Sunday, September 13, 2015

Digestive Enzymes

The primary enzymes of concem in the nutritional and functional food arena have been the hydrolases, so named because they catalyzethe breakdown of the substrate by adding a water molecule. The main classes of hydrolytic enzymes are protease (act on proteins), amylase (act on carbohydrates), lipase (act on fats or lipids) and cellulase (plant cellulose). Enzymes are important substances found naturally in the body and in food. If someone does not produce enough enzymes to properly breakdown their food, they can experience symptoms such as gas, constipation, bloating and heartburn. Raw foods also provide enzymes that naturally break down food for proper absorption. Supplemental enzymes typically come from two sources, either extracted from the pancreas of animals or prepared from plant products. Enzymes can improve the digestion of food, reduce stress in the gastrointestinal (GI) tract, help maintain normal pH levels and promote the growth of healthy intestinal flora. Many foods contain the enzymes necessary for their digestion.


Plant based enzymes are usually derived from the fungus Aspergillus oryzae. Several human studies suggest that these enzymes derived from this fungus may play a role in anti-inflammatory and fibrinolytic therapy, as well as providing digestive support. These enzymes may be, in some cases, more effective at digesting food than pancreatic based enzymes because their activity is not dependent on an optimal acid-alkaline environment.
Optimal pH is the range of acidity or alkalinity in which the digestive activity is the greatest. Plant-derived enzymes operate effectively at a very wide pH range, digesting actively in the (hopefully) acidic environment of the stomach and the alkaline environment of the small intestine.

Pancreatic enzymes improve digestion and assimilation of proteins and other nutrients as well as reduce circulating immune complexes that are formed from antigen and antibody reactions (i.e., allergies). They are more easily degraded than plant enzymes, and may be less effective for supporting digestive activity, since pancreatic enzymes are only effective in the slightly alkaline environment of the small intestine. Digestive enzymes are also found naturally in raw pineapple (bromelain) and green papaya (papain) as well as other foods, but these are weak compared to pancreatic or plant enzyme supplements.
Digestive enzyme supplementation is believed to be helpful for a large number of health conditions, including:

Pancreatic Insufficiency - Oral enzymes are standard medical treatment for conditions in which the pancreas is unable to meet the body's demands for enzyme production, such as cystic {ibrosis and malabsorption syndromes.
Food Allergies - By breaking down larger protein molecules into smaller, less allergenic molecules.
Inflammatory Bowel Disease (Crohn's and Ulcerative Colitis) - Some studies have shown enzyme deficiencies in these conditions.
Circulation - Enzymes taken on an empty stomach decrease break down of immune complexes and improve circulation.
Digesti Plant based enzymes appear to not only improve break down of macronutrients but also improve hydrochloric acid production in those with low stomach acid.
Parasites - Enzymes appear to help fight off certain parasites by weakening their protective coats.
Pain/lnflammation - Some find help lrom using digestive or pancreatic enzymes or bromelain/curcumin as anti-inflammatory agents that reduce swelling and help clear away debris from the injured area, such as after a sports injury or surgery.
Respiratory - Studies in Europe have shown that pancreatic enzymes speed recovery from bronchitis.
Pancreatic Cancer - Dr. Gonzales, MD pioneered working with cancer patients with pancreatic enzymes. He reviewed and published the follow-up results of 11 patients who followed his treatment regime. They lived on average three times longer than expected. Gonzales said all the patients were in an advanced stage of the illness, and their conditions were inoperable.  

Acne Rosacea - Digestive insufficiency is common in rosacea and enzyme supplementation may improve this skin condition.
Other Cancers - By supporting digestion, enzymes may increase the life expectancy in those suffering from many types of cancer.

For example, 166 subjects with multiple myeloma who took pancreatic enzyme tablets for the first year and then 1 tablet for the second year of the study experienced an extended lifespan from 47 months to 83 months over those who did not use the enzymes. 
A large study of patients with colorectal cancer who had previously undergone traditional therapies found that the addition of oral enzyme therapy (Wobe Mugos) improved their quality of life by reducing signs and symptoms of disease as well as reducing the adverse reactions to chemother.

Enzyme Potency

Enzyme potency is best defined in terms of activity, not weight. Weight measurements can be misleading as there is no direct relationship between weight and activity. Low potency enzymes may weigh as much as high potency ones, and filler may add to the weight (but, not the activity) of an enzyme supplement.Enzyme supplements come labeled with various units of measurement used to detect enzyme activity.
For each specific enzyme assay, the test to determine the activity of the erzyme must be performed under a specific substrate, pH and temperature. This makes it difficult to compare products with different assays.

Two independent scientific organizations have attempted to standardize ingredients used in foods and dietary supplements. The Committee on Food Chemicals Codex (FCC), a division of the US Institute of Medicine, publishes the Food Chemicals Codex.This reference manuai includes monographs and testing methods for a range of food chemicals, including many enzymes. FCC focuses on food grade ingredients, and its assays are more generally used for microbial and plant-based enzymes. The US Pharmacopeia (USP) also publishes standard assays for many pharmaceutical and nutraceutical ingredients. USP's testing is generally directed more toward pharmaceutical use enzymes and its methodology is more often employed for assaying animal-derived erzymes.

The following is a list of some of the enzyme units or assays used to detect enzyme activity: 
ALU - measures activity of acid lactase units (enzyme that breaks down milk sugar).
HUT - Measures the activity of protease enzymes (protein digesting enzymes) based on hemoglobin units on tyrosine basis
FCCLU - Measures the activity of lipase units (fat digesting enzymes).
FCCPU - Measures plant proteolytic activity (plant enzymes that break down protein).
r DU - Measures activity of amylase in dextrinizing units (carbohydrate digesting enzymes).
GDU - Measures the proteolytic activity of bromelain (enzyme that breaks down protein).

The US Pharmacopeia (USP) will appear as the number of times an enzyme is stronger than the standard. For example,"4Xpancreatin" is four times stronger than the USP standard. Each "X" contains 25 USP units of amylase, 2 USP units of lipase, and 25 USP units of protease (or proteolyic enzymes).
In theory, too much enzyame activity could be irritating as the enzymes travel through the digestive system. Fortunately, that does not usually happen with supplemental amounts.
Research has not determined the level at which such problems might arise. However, a serious condition involving damage to the large intestines called fibrosing colonopathy has resulted from the use of pancreatic enzymes in children with cystic fibrosis. Until more is known, children with cystic fibrosis needing to take pancreatic enzymes should only do so under the careful supervision of a knowledgeable healthcare professional-

Sunday, August 30, 2015

Insulin and Insulin Resistance – The Ultimate Guide

by Authority Nutrition 

Insulin is an important hormone that controls many processes in the body.
However, problems with this hormone are at the heart of many modern health conditions.
Sometimes our cells stop responding to insulin like they are supposed to.
This condition is termed insulin resistance, and is incredibly common.
In fact, a 2002 study showed that 32.2% of the US population may be insulin resistant (1).
This number may rise to 70% in obese adult women and over 80% in some patient groups (2, 3). About a third of obese children and teenagers may also have insulin resistance (4).
These numbers are scary, but the good news is that insulin resistance can be dramatically improved with simple lifestyle measures.
This article explains what insulin resistance is, why you should care and how you can overcome it.

Insulin and Insulin Resistance Explained

Highlighted Pancreas

Insulin is a hormone secreted by an organ called the pancreas.
Its main role is to regulate the amount of nutrients circulating in the bloodstream.
Although insulin is mostly implicated in blood sugar management, it also affects fat and protein metabolism.
When we eat a meal that contains carbohydrates, the amount of blood sugar in the bloodstream increases.
This is sensed by the cells in the pancreas, which then release insulin into the blood.
Then insulin travels around the bloodstream, telling the body’s cells that they should pick up sugar from the blood and bring it into the cells.
This leads to reduced amounts of sugar in the blood, and puts it where it is intended to go, into the cells for use or storage.
This is important, because high amounts of sugar in the blood can have toxic effects, causing severe harm and potentially leading to death if untreated.
However, due to various reasons (discussed below), sometimes the cells stop responding to the insulin like they are supposed to.
In other words, they become “resistant” to the insulin.
When this happens, the pancreas start producing even more insulin to bring the blood sugar levels down. This leads to high insulin levels in the blood, termed hyperinsulinemia.
This may continue to develop for a long time. The cells become increasingly more insulin resistant, and both insulin and blood sugar levels go up.
Eventually, the pancreas may not be able to keep up anymore and the cells in the pancreas may become damaged.
This leads to decreased insulin production, so now there are low amounts of insulin and cells that don’t respond to the little insulin that is available. This can lead to skyrocketing blood sugar levels.
When blood sugar levels exceed a certain threshold, a diagnosis of type 2 diabetes is made. In fact, this is a simplified version of how type 2 diabetes develops.
Insulin resistance is the main cause of this common disease that affects about 9% of people worldwide (5).

Resistance vs Sensitivity

Insulin resistance and insulin sensitivity are two sides of the same coin.
If you are insulin resistant, then you have low insulin sensitivity. Conversely, if you are insulin sensitive then you have low insulin resistance.
Being insulin resistant is a bad thing, while being insulin sensitive is good.
Bottom Line: Insulin resistance implies that the cells are not responding well to the hormone insulin. This causes higher insulin levels, higher blood sugar levels and may lead to type 2 diabetes and other health problems.

What Causes Insulin Resistance?

There are many potential causes and contributors to insulin resistance.

One of the main ones is believed to be increased amount of fats in the blood.
Numerous studies show that high amounts of free fatty acids in the blood cause cells, such as muscle cells, to stop responding properly to insulin (6, 7, 8).
This may be partly caused by fats and fatty acid metabolites building up inside muscle cells, termed intramyocellular fat. This disrupts the signalling pathways needed for insulin to work (9, 10, 11).
The main cause of elevated free fatty acids is eating too many calories and carrying excess body fat. In fact, overeating, weight gain and obesity are all strongly associated with insulin resistance (12, 13, 14, 15).
Having increased visceral fat, the dangerous belly fat that builds up around the organs, seems to be very important.
This type of fat may release lots of free fatty acids into the blood, and can even release inflammatory hormones that drive insulin resistance (16, 17, 18).
However, normal weight or thin people can also be insulin resistant, it is just much more common among those who are overweight (19).
There are several other potential causes of insulin resistance:
  • Fructose: A high intake of fructose (from added sugar, not fruit) has been linked to insulin resistance in both rats and humans (20, 21, 22).
  • Inflammation: Increased oxidative stress and inflammation in the body may lead to insulin resistance (23, 24).
  • Inactivity: Physical activity increases insulin sensitivity, and being inactive causes insulin resistance (25, 26).
  • Omega-3: Eating omega-3 fatty acids can in many cases reduce insulin resistance. They can also lower blood triglycerides, which are often high in insulin resistant people (27, 28).
  • Gut microbiota: There is evidence that a disruption in the bacterial environment in the gut can cause inflammation that exacerbates insulin resistance and other metabolic problems (29).
There are also various genetic and social factors, and blacks, Hispanics and Asians are at particularly high risk (30, 31, 32).
This list is not definitive. There are many other factors that may affect insulin resistance/sensitivity.
Bottom Line: The main causes of insulin resistance may be overeating and increased body fat, especially in the belly area. Other factors include high sugar intake, inflammation, inactivity and genetics.

How to Know if You Are Insulin Resistant

There are several ways that your doctor can determine if you are insulin resistant.
For example, having high fasting insulin levels is a good sign that you have insulin resistance.
A test called HOMA-IR estimates insulin resistance based on your blood sugar and insulin levels, and is fairly accurate.
There are also ways to measure blood sugar control more directly, such as an oral glucose tolerance test, where you are given a dose of glucose and then your blood sugar levels are measured for a few hours.
If you are overweight or obese, especially with large amounts of fat around the belly area, then chances are very high that you are insulin resistant.
There is also a skin condition called acanthosis nigrans, involving dark spots on the skin that can indicate insulin resistance.
Having low HDL (“good” cholesterol) levels and high blood triglycerides are two other markers that are strongly associated with insulin resistance (3).
Bottom Line: Having high insulin levels and high blood sugar levels are key symptoms of insulin resistance. Other symptoms include lots of belly fat, high blood triglycerides and low HDL levels

Insulin Resistance, Metabolic Syndrome and Type 2 Diabetes

Insulin resistance is a hallmark of two very common conditions, metabolic syndrome and type 2 diabetes.
Doctor Holding a Sign That Says Diabetes

The metabolic syndrome is a group of risk factors associated with type 2 diabetes, heart disease and other problems.
The symptoms are high blood triglycerides, low HDL levels, elevated blood pressure, central obesity (belly fat) and elevated blood pressure (33).
Sometimes this condition is referred to as the “insulin resistance syndrome” (34)
Insulin resistance is also a major driver of type 2 diabetes. The high blood sugar levels are caused by the cells not responding to insulin anymore (35).
Over time, the insulin-producing cells in the pancreas may stop functioning, leading to insulin deficiency as well (36).
By stopping the development of insulin resistance, it may be possible to prevent most cases of metabolic syndrome and type 2 diabetes.
Bottom Line: Insulin resistance is at the heart of metabolic syndrome and type 2 diabetes, which are currently among the biggest health problems in the world.

Insulin Resistance is Linked to Heart Disease and All Sorts of Other Health Problems

Insulin resistance is also strongly associated with heart disease, which is the world’s biggest killer (37).
In fact, people who are insulin resistant or have metabolic syndrome have up to a 93% greater risk of heart disease (38).
There are many other diseases linked to insulin resistance. This includes non-alcoholic fatty liver disease, polycystic ovarian syndrome (PCOS), Alzheimer’s disease and cancer (39, 40, 41, 42).
Bottom Line: Insulin resistance may cause a variety of diseases, including heart disease, non-alcoholic fatty liver disease, polycystic ovarian syndrome, Alzheimer’s disease and cancer.

Ways to Reduce Insulin Resistance (Improve Insulin Sensitivity)

The good thing about insulin resistance, is that it is very easy to influence it.
In fact, changing your lifestyle is able to completely reverse insulin resistance in many cases.
Here are several evidence-based ways to reduce insulin resistance:
  1. Exercise: This may be the single easiest way to improve insulin sensitivity. The effect is almost immediate (43, 44).
  2. Lose belly fat: Try to lose some fat, especially the deep “visceral” fat from your liver and belly. This article lists several evidence-based tips on how to lose belly fat.
  3. Stop Smoking: Tobacco smoking can cause insulin resistance, so quitting should help (45)
  4. Sugar: Try to reduce your intake of added sugars, especially from sugar-sweetened beverages.
  5. Eat healthy: Eat a diet based mostly on whole, unprocessed foods. Include nuts and fatty fish.
  6. Supplements: Taking a supplement called berberine can be effective to enhance insulin sensitivity and reduce blood sugar (46). Magnesium supplements may be helpful as well (47).
  7. Sleep: There is some evidence that poor sleep causes insulin resistance, so improving sleep quality should help (48).
  8. Stress: If excessive, try to manage your stress levels (49). Meditation has been shown to be helpful (50).
  9. Donate blood: High levels of iron in the blood are linked to insulin resistance. For men and postmenopausal women, donating blood may improve insulin sensitivity (51, 52, 53).
  10. Intermittent fasting: Following an eating pattern called intermittent fasting can improve insulin sensitivity (54).
Most of the items on the list also happen to be the same things we generally associate with good health, protection against disease and a long life.
All this being said, keep in mind that nothing in this article is intended as medical advice.
Insulin resistance is linked to various serious health problems, and I recommend that you speak to your doctor about your options. There are also various medical treatments that can work.
Bottom Line: Insulin resistance may be reduced or even completely reversed with simple lifestyle measures. These include exercise, eating healthy, losing belly fat and taking care of your sleep and stress levels.

Low-Carb Diets and Insulin Resistance

Another thing worth highlighting is low-carb diets.
Diets that restrict carbohydrates can have incredibly powerful benefits against metabolic syndrome and type 2 diabetes (55, 56), and this is partly mediated by reduced insulin resistance (57, 58, 59).
However, when carb intake is very low, such as on a ketogenic diet, the body may induce an insulin resistant state in order to spare blood sugar for the brain.
This is termed “physiological” insulin resistance (as opposed to “pathological”) and is not a bad thing (60).
Bottom Line: Low-carb diets reduce the harmful insulin resistance linked to metabolic disease. However, very low-carb ketogenic diets may induce a harmless type of insulin resistance that spares blood sugar for the brain.

Take Home Message

Insulin resistance may be one of the key drivers of many (if not most) of today’s chronic diseases, which are collectively killing millions of people every year.
The good news is that it can be significantly improved with simple lifestyle measures, such as losing fat, eating healthy food and exercising.
Preventing insulin resistance may be among the single most powerful things you can do to live a longer, healthier and happier life.

Sunday, August 23, 2015

The “Chemical Imbalance” in Mental Health Problem

This article has been developed and written for use as a patient handout. It may be reproduced/copied to provide patient information.
Introduction
Over the years, advances in neurology and research have simplified the way psychologists, psychiatrists, and others diagnosis and treat mental health problems. In over one hundred years of mental health treatment, the symptoms and behaviors associated with certain mental health conditions have remained the same. Psychotic disorders, where the individual often can’t distinguish between reality and their fantasies, still have auditory hallucinations. Depressed individuals still can’t sleep and remain preoccupied with the past. Hyperactive children (Attention-Deficit Hyperactivity Disorder or ADHD) still exhibit uncontrollable restlessness. 

When patients first began reclining on the couches of psychoanalytic psychiatrists, the depressed folks talked about their past. This led the founders of psychology and psychiatry to believe that issues that began in childhood caused many mental health problems. But questions were still not answered. Why would a bad relationship with your mother create the appetite loss found in depression, especially when eating problems only started several months prior to the session? By what strange mechanism would a childhood issue create an auditory hallucination, often years after the reported traumatic event? Many people had difficult childhoods, but they didn’t hallucinate and have a great appetite. It became clear that many mental health problems also had a physical component that involved changes in concentration, sleep, appetite, speech pattern, energy level, perceptions (hallucinations), and motivation. Studies began to determine the connection, if indeed one was present, between the condition of the patient and the physical signs/symptoms that were also present.

The picture became easier to understand when chemicals in the brain called “neurotransmitters” were discovered. The brain consists of billions of neurons or cells that must communicate with each other. The communication between neurons maintains all body functions, informs us when a fly lands on our hand, or when we have pain. The communication between neurons is controlled by the brain’s type and level of neurotransmitters. Neurotransmitters are chemical substances that control and create signals in the brain both between and within neurons. Without neurotransmitters, there would be no communication between neurons. The heart wouldn’t get a signal to beat, arms and legs wouldn’t know to move, etc.

As we discovered more about neurotransmitters, we began to identify which neurotransmitters controlled certain bodily functions or which were related to certain emotional/psychiatric difficulties. Serotonin, a neurotransmitter, was found to be related to body temperature and the onset of sleep. Research also identified Serotonin as related to depression and later to a variety of mental health conditions such as anorexia and obsessive-compulsive disorder. 

As research in neurotransmitters continued, studies between neurotransmitters and mental conditions revealed a strong connection between amounts of certain neurotransmitters in the brain and the presence of specific psychiatric conditions. Using an everyday example, our automobile operates by using a variety of fluids such as engine oil, transmission fluid, brake fluid, and coolant (anti-freeze). Every automobile has a way to measure the levels or amounts of each of these needed liquids such as the dipstick for oil and transmission fluid and marked indicators for anti-freeze and brake-fluid levels. Using our dipstick to measure engine oil, for an example, we can find our engine to be found one, two, or even three quarts low. After a recent oil change, the dipstick may also tell us that we have excessive oil in the engine. To work properly, all fluid levels must be in the “normal range” as indicated by the dipstick. When we receive a blood test, values of certain blood components are given with the “normal range” also provided, indicating if a blood chemical is below or above the average range. 

Neurological research has identified over fifty (50) neurotransmitters in the brain. Research also tells us that several neurotransmitters are related to mental health problems – Dopamine, Serotonin, Norepinephrine, and GABA (Gamma Aminobutyric Acid). Too much or too little of these neurotransmitters are now felt to produce psychiatric conditions such as schizophrenia, depression, bi-polar disorder, obsessive-compulsive disorder, and ADHD.
Unfortunately, the body doesn’t have a built-in dipstick for neurotransmitters, at least one that’s inexpensive enough for community mental health practice. There are advanced imaging techniques such as Positron Emission Tomography (PET Scans) that are being utilized in research and in the development of medications that directly influence changes in specific neurotransmitters. Lacking a PET Scanner, most professionals evaluate neurotransmitter levels by looking for indicators in thought, behavior, mood, perception, and/or speech that are considered related to levels of certain neurotransmitters.

This is perhaps best illustrated in individuals with depressed mood. The mental health professional is often required to separate those who would benefit from counseling and those who may require counseling and an antidepressant medication. The key is looking for those symptoms that are known to be related to chemical changes in the brain. For example, situational depression often produces sad expressions, worry, pessimistic attitude and other features but does not create prolonged changes in the physical symptoms such as changes in sexual interest, appetite, or sleep. The continued presence of physical symptoms tells us that the brain’s neurotransmitter levels have changed.

The technical aspects of neurotransmitter levels, the psychiatric symptoms they produce, and how medications have been developed to raise or lower the brain levels of these neurotransmitters can be very complicated. For this reason, the same procedure of explaining other medical conditions where medication brings symptoms back to the “normal range” is often used. Medical patients with high blood pressure, high blood sugar, or high cholesterol are informed that their body chemistry is too high, or in some cases, too low and must be corrected with medication.
For many years, mental health professionals have used the term “chemical imbalance” to explain the need for medications that are used to treat mental health conditions. This simple and commonly used explanation recognizes that the condition is a medical problem and that it can be treated with medication. The “chemical imbalance” explanation also reflects the overall theme of treatment – identifying what neurotransmitters are involved in the clinical symptom picture and with medication, attempting to return that neurotransmitter level back to the “normal range”. 

Your Neurotransmitter Levels and Emotional Health
Your emotional health is a combination of attitudes, personality, support systems, and your brain’s neurotransmitter levels. Positive attitudes and a healthy personality help us through life’s difficulties and a good support system of family and friends is also valuable during times of trouble. Despite having these resources, there are times when coping with our experiences and life events changes our neurotransmitter status. Like an overheated automobile, we begin to have difficulty operating properly.
We are all at-risk for changes in our brain’s chemistry. Mostly commonly, we will experience depression, anxiety, or stress reactions. As our neurotransmitters change, they bring with them additional symptoms, behaviors, and sensations that add to our on-going difficulties. Recognizing these changes is an important part of treatment and returning your life to normal and reducing our stress.
This discussion is offered to explain how the neurotransmitter system in the brain can create psychiatric conditions and mental health problems. It is hoped the discussion will provide information that will be of value to those who suspect their neurotransmitter system is creating problems.
The following is a discussion of neurotransmitters and current thoughts about how these neurochemicals are involved in psychiatric illness. Four neurotransmitters, out of over fifty, are well researched and known to be related to psychiatric conditions. 

Dopamine: Parkinson’s Disease and ADHD to Smoking and Paranoia
Dopamine is a neurotransmitter linked to motor/movement disorders, ADHD, addictions, paranoia, and schizophrenia. Dopamine strongly influences both motor and thinking areas of the brain.
One type of Dopamine works in the brain movement and motor system. As this level of dopamine decreases below the “normal range” we begin to experience more motor and gross-movement problems. Very low levels of Dopamine in the motor areas of the brain are known to produce Parkinson’s Disease with symptoms such as:
Muscle rigidity and stiffness
Stooped/unstable posture
Loss of balance and coordination
Gait (walking pattern) disturbance
Slow movements and difficulty with voluntary movements
Small-step gait/walking
Aches in muscles
Tremors and shaking
Fixed, mask-like facial expression
Slow, monotone speech
Impairment of fine-motor skills
Falling when walking
Impairment in cognitive/intellectual ability
Dopamine in the thinking areas of the brain might be considered the neurotransmitter of focus and attending. Low levels impair our ability to focus on our environment or to “lock on” to tasks, activities, or conversations. Low levels of Dopamine make concentration and focus very difficult with low levels also associated with Attention-Deficit Hyperactivity Disorder (ADHD). On the other end of the Dopamine dipstick, as Dopamine levels in the brain begin to raise, we become excited/energized, then suspicious and paranoid, then finally hyperstimulated by our environment. With low levels of Dopamine, we can’t focus while with high levels of Dopamine our focus becomes narrowed and intense to the point of focusing on everything in our environment as though it were directly related to our situation.

Mild elevations in Dopamine are associated with addictions. Nicotine, cocaine, and other substances produce a feeling of excited euphoria by increasing Dopamine levels in the brain. Too much of these chemicals/substances and we feel “wired” as moderate levels of Dopamine make us hyperstimulated – paying too much attention to our environment due to being overstimulated and unable to separate what’s important and what is not. 

In an ADHD child, low levels of Dopamine don’t allow the child to focus or attend to anything in the environment, looking very physically hyperactive when running about the room or switching from activity-to-activity due to their lack of focus. As Dopamine levels increase above the normal range, our ability to focus increases to the point of being paranoid. Mild elevations make the environment overly stimulating and excited. 

Moderately high Dopamine levels make us on-guard, suspicious, and prone to misinterpret experiences in the environment. Known as an “idea of reference” in psychiatry, we begin thinking unrelated experiences are suddenly directly related to us. People observed talking across the street are now talking about us. As Dopamine increases, it can become so intense that we feel the radio, television, and newspaper contain secret messages directed at us from Hollywood or elsewhere. It’s as though we are attempting to incorporate/add everything we witness into our life. Planes flying overhead are snapping pictures of us and motorists talking on cellular phones are calling in a report on us. Our mind speed increases and races in an attempt to add all we see into our life. In an attempt to make sense, we may become extremely religious, paranoid, or feel we are a very important person. Increased Dopamine also increases the perception of our senses, as though turning up the volume in all our senses – hearing, vision, taste, smell, and touch.

As Dopamine levels increase, the noises we heard loudly suddenly become auditory hallucinations. Our inner thoughts are now being heard outside our body. These “voices” begin talking to us, known to take different forms such as derogatory (putting you down), religious topics, command (telling you to do something), or sexual content. Hallucinations (experiencing something that is not truly there in reality) will soon develop in all our senses. We may begin seeing faces in clouds, carpets, or patterns. We may sense the touch of spirits or movements inside our body. We may experience unusual smells or tastes.

High levels of Dopamine in the brain often cause us to lose our contact with reality. As though living in a science-fiction movie, we begin to develop unusual if not bizarre ideas about what is happening to us. With our paranoia, we may experience delusions (false beliefs) of persecution or may think we have super powers (delusions of grandiosity) and can predict the future or read minds. High levels of Dopamine are found in Schizophrenia, drug intoxication, and other psychotic conditions where the ability to distinguish the inner world from the real world is impaired.

Treatment for psychiatric/medical conditions associated with Dopamine imbalance, as you might expect, involves increasing or decreasing Dopamine levels in the brain. Low-Dopamine disorders are treated with medications that increase Dopamine in the brain. For Parkinson’s Disease – L Dopa is prescribed and for ADHD, medications that are psychostimulants. Amphetamines and medications with similar action actually slow down the hyperactive (ADHD) children by increasing Dopamine – boasting their level into the normal range, allowing them to now focus and attend.

Mildly elevations in Dopamine are associated with addictions such as narcotics, speed, and nicotine/smoking. Thus, medications used in the treatment of addictions actually block or lower Dopamine production. If a medication blocks dopamine, it also blocks the effects of the addicted substance as well as blocking the craving sensation. The medication to help smokers, Zyban, is actually the antidepressant Wellbutrin that is known to block Dopamine.

Moderate to high levels of Dopamine, associated with severe psychiatric conditions such as Paranoia and Schizophrenia, are treated with medications that block or lower Dopamine in the brain. These medications, called antipsychotics, have been available for many years. Early antipsychotic medications however, lowered Dopamine throughout the brain, including the Dopamine located in the motor/movement areas. For that reason, older antipsychotic medications produced motor/movement problems that looked like Parkinson’s Disease – short-step gait, fixed facial expression, tremors, poor balance, etc. Newer medications have fewer side effects in motor areas, as they are able to specifically target one type of Dopamine.

Dopamine levels typically change very slowly. Patients who develop Paranoia and/or Schizophrenia often experience a gradual increase in Dopamine levels over several years – also experiencing an increase in the severity of symptoms over those years. A typical high school or college student may develop a sense of being on-edge or unusual feelings, gradually becoming suspicious and feeling alienated, moving into auditory hallucinations, and finally developing bizarre false beliefs (delusions) of persecution or exaggerated self-importance over the next several years. Stress can often rapidly increase Dopamine, but it still rarely happens overnight.
When an individual becomes psychotic, paranoid, and hallucinates in only a few days, we must strongly suspect medication/drug intoxication or neurological events – something that could increase Dopamine levels dramatically and almost instantly. The prolonged use of amphetamines (speed) or steroids can produce a loss of reality and sudden paranoia. As it might happen, a construction worker taking “street” speed to increase his work productivity finds his hand or foot talking to him (auditory hallucinations) and decides to cut it off. The sudden presence of psychosis (hallucinations, delusions, paranoia, etc.) in an individual with a history of prior normal adjustment would suggest the need for intensive medical and neurological workup.

Serotonin: From Bliss to Despair
Serotonin, first isolated in 1933, is the neurotransmitter that has been identified in multiple psychiatric disorders including depression, obsessive-compulsive disorder, anorexia, bulimia, body dysmorphic disorder (nose doesn’t look perfect after ten surgeries), social anxiety, phobias, etc. Serotonin is a major regulator and is involved in bodily processes such as sleep, libido (sexual interest), body temperature, and other areas.
Perhaps the best way to think of Serotonin is again with an automobile example. Most automobiles in the United States are made to cruise at 70 miles per hour, perfect for interstate highways and that summer vacation. If we place that same automobile on a racetrack and drive day-after-day at 130 mph, two things would happen. Parts would fail and we would run the engine so hot as to evaporate or burnout the oil. Serotonin is the brain’s “oil”.
Like a normal automobile on a race track, when we find ourselves living in a high stress situation for a prolonged period of time, we use more Serotonin than is normally replaced. Imagine a list of your pressures, responsibilities, difficulties and environmental issues (difficult job, bad marriage, poor housing, rough neighborhood, etc.). Prolonged exposure to such a high level of stress gradually lowers our Serotonin level. As we continue to “hang on” we develop symptoms of a severe stress-produced depression. 

An automobile can be one, two or three quarts low in oil. Using the automobile as an example, imagine that brain Serotonin can have similar stages, being low (one quart low), moderately low (two quarts low), and severely low (three quarts low). The less Serotonin available in the brain, the more severe our depression and related symptoms.
When Serotonin is low, we experience problems with concentration and attention. We become scatterbrained and poorly organized. Routine responsibilities now seem overwhelming. It takes longer to do things because of poor planning. We lose our car keys and put odd things in the refrigerator. We call people and forget why we called or go to the grocery and forget what we needed. We tell people the same thing two or three times. 

As stress continues and our Serotonin level continues to drop, we become more depressed. At this point, moderately low or “two quarts” low, major changes occur in those bodily functions regulated by Serotonin. When Serotonin is moderately low, we have the following symptoms and behaviors:
· Chronic fatigue. Despite sleeping extra hours and naps, we remain tired. There is a sense of being “worn out”
· Sleep disturbance, typically we can’t go to sleep at night as our mind/thought is racing. Patients describe this as “My mind won’t shut up!” Early-morning awakening is also common, typically at 4:00 am, at which point returning to sleep is difficult, again due to the racing thoughts.
· Appetite disturbance is present, usually in two types. We experience a loss of appetite and subsequent weight loss or a craving for sweets and carbohydrates when the brain is trying to make more Serotonin.
· Total loss of sexual interest is present. In fact, there is loss of interest in everything, including those activities and interests that have been enjoyed in the past.
· Social withdrawal is common – not answering the phone, rarely leaving the house/apartment, we stop calling friends and family, and we withdraw from social events.
· Emotional sadness and frequent crying spells are common.
· Self-esteem and self-confidence are low.
· Body sensations, due to Serotonin’s role as a body regulator, include hot flushes and temperature changes, headaches, and stomach distress.
· Loss of personality – a sense that our sense of humor has left and our personality has changed.
· We begin to take everything very personally. Comments, glances, and situations are viewed personally and negatively. If someone speaks to you, it irritates you. If they don’t speak, you become angry and feel ignored.
· Your family will have the sense that you have “faded away”. You talk less, smile less, and sit for hours without noticing anyone.
· Your behavior becomes odd. Family members may find you sitting in the dark in the kitchen at 4:00 am.
Individuals can live many years moderately depressed. They develop compensations for the sleep and other symptoms, using sleeping medication or alcohol to get some sleep. While chronically unhappy and pessimistic, they explain their situation with “It’s just my life!” They may not fully recognize the depressive component.
Very low levels of Serotonin typically bring people to the attention of their family physician, their employer, or other sources of help. Severe Serotonin loss produces symptoms that are difficult to ignore. Not only are severe symptoms present, but also the brain’s ideation/thinking becomes very uncomfortable and even torturing. When Serotonin is severely low, you will experience some if not all of the following:

· Thinking speed will increase. You will have difficulty controlling your own thoughts. The brain will focus on torturing memories and you’ll find it difficult to stop thinking about these uncomfortable memories or images.

· You’ll become emotionally numb! You wouldn’t know how you feel about your life, marriage, job, family, future, significant other, etc. It’s as though all feelings have been turned off. Asked by others how you feel – your response might be “I don’t know!”

· Outbursts will begin, typically two types. Crying outbursts will surface, suddenly crying without much warning. Behavioral outbursts will also surface. If you break the lead in a pencil, you throw the pencil across the room. Temper tantrums may surface. You may storm out of offices or public places.
· Escape fantasies will begin. The most common – Hit the Road! The brain will suggest packing up your personal effects and leaving the family and community. 

· Memory torture will begin. Your brain, thinking at 100 miles an hour, will search your memories for your most traumatic or unpleasant experiences. You will suddenly become preoccupied with horrible experiences that may have happened ten, twenty, or even thirty years ago. You will relive the death of loved ones, divorce, childhood abuse – whatever the brain can find to torture you with – you’ll feel like it happened yesterday.

· You’ll have Evil Thoughts. New mothers may have thoughts about smothering their infants. Thoughts of harming or killing others may appear. You may be tortured by images/pictures in your memory. It’s as though the brain finds your most uncomfortable weak spot, then terrorizes you with it.

· With Serotonin a major bodily regulator, when Serotonin is this low your body becomes unregulated. You’ll experience changes in body temperature, aches/pains, muscle cramps, bowel/bladder problems, smothering sensations, etc. The “Evil Thoughts” then tell you those symptoms are due to a terminal disease. Depressed folks never have gas – it’s colon cancer. A bruise is leukemia. 

· You’ll develop a Need-for-Change Panic. You’ll begin thinking a change in lifestyle (Midlife Crisis!), a divorce, an extramarital affair, a new job, or a Corvette will change your mood. About 70 percent of jobs are lost at this time as depressed individuals gradually fade away from their life. Most extramarital affairs occur at this time.

· As low Serotonin levels are related to obsessive-compulsive disorders, you may find yourself starting to count things, become preoccupied with germs/disease, excessively worry that appliances are turned off or doors locked, worry that televisions must be turned off on an even-numbered channel, etc. You may develop rituals involving safety and counting. One auto assembly plant worker began believing his work would curse automobiles if their serial number, when each number was added, didn’t equal an even number. 

· Whatever normal personality traits, quirks, or attitudes you have, they will suddenly be increased three-fold. A perfectionist will suddenly become anxiously overwhelmed by the messiness of their environment or distraught over leaves that fall each minute to land on the lawn. Penny-pinchers will suddenly become preoccupied with the electric and water consumption in the home.
· A “trigger” event may produce bizarre behavior. Already moderately low in Serotonin, an animal bite or scratch may make you suddenly preoccupied with rabies. A media story about the harmful effects of radiation may make you remember a teenage tour of the local nuclear power plant – suddenly feeling all your symptoms are now the result of exposure to radiation.

· When you reach the bottom of “severely low” Serotonin, the “garbage truck” will arrive. Everyone with severely low Serotonin is told the same thing. You will be told 1) You’re a bad spouse, parent, child, employee, etc., 2) You are a burden to those who love or depend on you, 3) You are worsening the lives of those around you, 4) Those who care about you would be better if you weren’t there, 5) You would be better if you weren’t around, and 6) You and those around you would be better off if you were totally out of the picture. At that point, you develop suicidal thoughts.

Clinical Depression is perhaps the most common mental health problem encountered in practice. One in four adults will experience clinical depression within their lifetime. Depression is the “common cold” of mental health practice – very common and much easier to treat today than in the past.

Treatment for depression, as might be expected, involves increasing levels of Serotonin in the brain. Since the mid-eighties, medications have been available that attempt to specifically target and increase Serotonin. Known as Selective Serotonin Reuptake Inhibitors (SSRI’s), these medications such as Prozac, Zoloft, and Paxil are felt to work by making more Serotonin available in the brain.
Like all neurotransmitters, we can have too much Serotonin. While elevated levels of Serotonin produce a sense of well-being, bliss, and “oneness with the universe” – too much Serotonin can produce a life-threatening condition known as Serotonin Syndrome (SS). 

Likely to occur by accident by combining two Serotonin-increasing medications or substances, Serotonin Syndrome (SS) produces violent trembling, profuse sweating, insomnia, nausea, teeth chattering, chilling, shivering, aggressiveness, over-confidence, agitation, and malignant hyperthermia. Emergency medical treatment is required, utilizing medications that neutralize or block the action of Serotonin as the treatment for Serotonin Syndrome (SS).

Like Dopamine, Serotonin can be accidentally increased or decreased by substances. One method of birth control is known to produce severe depression as it lowers Serotonin levels. A specific medication for acne has also been linked with depression and suicidal ideation. For this reason, always inform your physicians if you are taking any medication for depression. Also avoid combining antidepressants with any herbal substances reported to be of help in Depression such as St. John’s Wort.

Norepinephrine: From Arousal to Panic
Norepinephrine (NE) is the neurotransmitter often associated with the “fight or flight” response to stress. Strongly linked to physical responses and reactions, it can increase heart rate and blood pressure as well as create a sense of panic and overwhelming fear/dread. This neurotransmitter is similar to adrenaline and is felt to set threshold levels to stimulation and arousal. Emotionally, anxiety and depression are related to norepinephrine levels in the brain, as this neurotransmitter seems to maintain the balance between agitation and depression.
Low levels of norepinephrine are associated with a loss of alertness, poor memory, and depression. Norepinephrine appears to be the neurotransmitter of “arousal” and for that reason, lower-than-normal levels of this neurotransmitter produce below-average levels of arousal and interest, a symptom found in several psychiatric conditions including depression and ADHD. It is for this reason that medications for depression and ADHD often target both dopamine and norepinephrine in an attempt to restore both to normal level.

Mild elevations in our norepinephrine levels produce heightened arousal, something known to be produced by stimulants. This arousal is considered pleasurable and several “street drugs” such as cocaine and amphetamines work by increasing the brains level of norepinephrine. This increased sense of arousal is pleasurable, linking these substances to their potential for addiction. Research tells us that some individuals using antidepressants develop a state of “hypomania” or emotional elation and physical arousal in this same manner. For that reason, individuals using modern antidepressants are often cautioned to notify their treating physician/psychiatrist if they become “too happy”.
Moderately high levels of norepinephrine create a sense of arousal that becomes uncomfortable. Remembering that this neurotransmitter is strongly involved in creating physical reactions, moderate increases create worry, anxiety, increased startle reflex, jumpiness, fears of crowds & tight places, impaired concentration, restless sleep, and physical changes. The physical symptoms may include rapid fatigue, muscle tension/cramps, irritability, and a sense of being on edge. Almost all anxiety disorders involve norepinephrine elevations.

Severe and sudden increases in norepinephrine are associated with panic attacks. Perhaps the best way to visualize a panic attack is to remember the association with the “flight or fight” response. The “flight or fight” response is a chemical reaction to a dramatic and threatening situation in which the brain produces excessive amounts of norepinephrine and adrenaline – giving us extra strength, increased energy/arousal, muscle tightness (for fighting or running), and a desperate sense that we must do something immediately. This animal response was activated in early man when a bear showed up at his cave or when faced with a tiger in the woods. In modern times, imagine your reaction if while calmly watching television, someone or something started trying to knock your front door in to attack you. In the “flight or fight” reaction, your brain and body chemistry prepare you to either run from the situation or fight to the death!

A panic attack is the activation of the “flight or fight” chemical reaction without a bear at the door. It’s as though the self-protection animal response is kicking-off accidentally, when no real life-threatening situation is present. Known now as panic attacks, they can surface at the grocery, at church, or when you least expect it. As norepinephrine is a fast-acting neurotransmitter, the panic attack may last less than ten minutes (feels like hours however!) but you’ll be rattled/shaken for several hours. Panic attacks are strong physical and chemical events and include the following symptoms:
· Palpitations, pounding heart or rapid heart rate
· Sweating and body temperature changes
· Trembling or shaking
· Shortness of breath of smothering sensations
· Choking sensations
· Chest pain and discomfort
· Nausea or stomach distress
· Dizziness, lightheadedness, or feeling faint
· Sense of unreality, as though you are outside yourself
· Fear of losing control or going crazy
· Fear of dying
· Numbness and tingling throughout the body
· Chills and hot flushes
If we think about the automobile example, a panic attack is the equivalent of your dashboard warning lights coming on – your stress level is too high. Panic attacks, or surges of norepinephrine, can also occur by accident as when created by the use of certain medications. The medications for certain medical conditions can cause a panic attack or increase our level of anxiety. Medications often used for asthma, for example, can create anxiety or panic attacks.

Treating low or elevated levels of norepinephrine in the brain involve different approaches. Low levels of norepinephrine are often treated using newer antidepressants. Many new antidepressants, known as Serotonin-Norepinephrine Reuptake Inhibitors (SNRI’s) with brand names like Effexor and Serzone, treat depression by increasing levels of both serotonin and norepinephrine neurotransmitters.
Treatment for high levels of norepinephrine, as found in anxiety and panic disorders, involves decreasing neurotransmitter levels directly or using medications which increase another neurotransmitter that inhibits or decreases the action of norepinephrine. One of those inhibiting neurotransmitters is GABA, also known as Gamma-Aminobutyric Acid.

GABA: Mania and Seizures to Relaxation and Impulse Control
Gamma-Aminobutyric Acid (GABA) is a neurotransmitter that is inhibitory, that is, it decreases the ability of other neurotransmitters to work. GABA is involved in our level of excitability. Rather than encouraging communication between cells such as Dopamine, Serotonin or Norepinephrine - GABA reduces, discourages, and blocks communication. This neurotransmitter is important in brain areas involving emotion and anxiety.

When GABA is in the normal range in the brain, we are not overly aroused or anxious. At the same time, we have appropriate reactions to situations in our environment. GABA is the communication speed controller, making sure all brain communications are operating at the right speed and with the correct intensity. Too little GABA in the brain, the communication becomes out of control, overstimulated, and chemically unstable. Too much GABA and we are overly relaxed and sedated, often to the point that normal reactions are impaired.

Low levels of GABA are associated with Bipolar Disorder, Mania. With GABA levels below average, the brain is too stimulated. We begin talking rapidly, staying up for days at a time, and develop wild and grandiose ideas. In a Manic state, we are so “high” and out of control that social problems are quick to develop, often due to hypersexuality, excessive spending, reckless decisions, risk-taking behavior, and grandiose ideas. We may feel so good that we think we are a heavenly spirit, an intellectual genius, or possessing extraordinary powers. I personally had one patient who locked himself in his mobile home and spent one week rewriting the New Testament in “hillbilly”. Another, with limited education, began purchasing books on the Theory of Relativity by Albert Einstein, sensing he may be able to use the information to invent “warp drive”.
Low levels of GABA are also associated with problems of poor impulse control, including clinical conditions such as gambling, temper tantrums, and stealing. When GABA is low in the brain, impulsive behaviors are not inhibited (stopped) by logical or reasonable thinking. 

Low levels of GABA are also associated with epilepsy or seizure disorders. If we imagine a seizure as a type of electrical storm, the seizure begins at one location in the brain then rushes across and through the brain like a sudden storm. Low levels of GABA make it easy for the brain to develop seizures which is why seizures are part of the withdrawal syndrome for many substances that work with GABA such as alcohol and tranquilizers (benzodiazepines – Xanax, Ativan, Librium, Valium, etc.). Substances that artificially maintain a high level of GABA, when stopped, create a dramatic drop in GABA levels, thus creating the risk for withdrawal seizures due to the chemical instability that is created.

High levels of GABA produce more control, relaxation, and even sedation. Alcohol works by increasing GABA levels, which is why all body systems are relaxed at first – then sedated to the point of slurred speech, unsteady gait, and foggy thinking. Alcohol withdrawal, or the sudden severe drop of high GABA levels, produce a low GABA level and the possibility of seizures. Withdrawal from benzodiazepines is known to follow the same pattern. Taking forty milligrams of Valium for two years, suddenly stopping all medication, will likely produce a seizure.
Medications for anxiety create relaxation and a decrease in anxiety by increasing GABA levels in the brain. Alcoholic beverages work in the same manner; the alcohol increasing GABA levels to produce mild euphoria, loss of social anxiety, and other symptoms of intoxication. Excessive intake of benzodiazepines and/or alcohol is extremely dangerous as the high GABA level actually smothers the communication between brain neurons – sometimes to the point of a total lack of communication between neurons – also known as death.

Medications for seizures, impulse control problems, and Bipolar Disorder, Mania all work by increasing the GABA levels without accompanying euphoria. Lithium and anti-seizure medications all increase GABA into the normal range, thus lowering the possibility of seizures and producing brain chemical stability. As GABA is the neurotransmitter policeman, changes in GABA can influence all neurotransmitters but especially norepinephrine.

Medication Treatment of the “Chemical Imbalance”
Understanding these four neurotransmitters provides a window to understanding the majority of psychiatric conditions, ranging from depression to schizophrenia. Mental health professionals use psychological testing, interviews, questionnaires, and patient history to determine first, if a change in the neurotransmitter system is present, then second, what neurotransmitters are involved. A proper clinical diagnosis then leads to proper medication treatment.

Medications are prescribed in an effort to return the brain’s neurotransmitter status to normal. Much like a physician may prescribe a medication to lower your cholesterol or increase another body chemical, mental health professionals are concerned with returning your neurotransmitter levels to normal.
Medications for mental health conditions work in several ways:
· Some imitate the neurotransmitter, triggering a response as though the original neurotransmitter were present
· Some block the neurotransmitter from being absorbed by the surrounding neurons, known as blocking the reuptake. Reuptake inhibitors block the reabsorption/reuptake of Serotonin or Norepinephrine and thus make more neurotransmitter available
· Some force the release of the neurotransmitter, causing an exaggerated effect. Cocaine does this to Norepinephrine and Dopamine while MDMA (Ecstasy – a club drug) does this to Serotonin.
· Some increase neurotransmitters known to slowdown or reduce the production of other neurotransmitters.
· Some block the release of neurotransmitters completely
· Some interfere with the storage of neurotransmitters, allowing them to come out of storage and lose potency
Based on the neurotransmitter theory of psychiatric illness, we can plot clinical conditions and see how mental health professionals determine medication treatment by recognizing which neurotransmitters are involved:
Diagnosis: Stress-Produced Depression
Neurotransmitter: Low Serotonin
Medication: Selective Serotonin Reuptake Inhibitor (SSRI)
Diagnosis: Agitated/Anxious Depression
Neurotransmitter: Low Serotonin
Elevated Norepinephrine
Medication: SSRI and Antianxiety Medication or
Serotonin Norepinephrine Reuptake Inhibitor (SNRI)
Diagnosis: Major Depression with Psychosis
(Severe depression with hallucinations/paranoia)
Neurotransmitter: Elevated Dopamine
Low Serotonin
Medication: Antipsychotic medication
SSRI
Diagnosis: Bipolar Disorder, Mania
Neurotransmitter: Low GABA
Medication: Anticonvulsant or Lithium
Diagnosis: Bipolar Disorder, Depressed
Neurotransmitter: Low GABA
Low Serotonin
Medication: Anticonvulsant or Lithium
SSRI

Final Thoughts
A variety of conditions and circumstances encountered in life can produce changes in our brain chemistry. These changes can then create mental health problems. We have known for years that chemical and substances in the body can become unregulated as in high blood pressure, high cholesterol, low/high blood sugar, etc. There is no stigma associated with using medications to return these body chemicals/substances back to their normal levels.

It is the hope of mental health professionals that the public can understand the medical and neurochemical nature of various emotional and psychiatric conditions, thus eliminating the stigma often associated with treatment. Modern treatment is very effective and can eliminate years of emotional suffering with very little in the way of intervention or treatment. Mental health treatment is available in every county in the United States.

This article is presented as a public service by Joseph M. Carver, Ph.D., a Clinical Psychologist

Sunday, July 12, 2015

David Wolfe's Top 10 Immunity Superheroes

Your immune system is vast and complex. It is designed to detoxify your body as well as protect it from illness and foreign invaders.


Harmful bacteria, viruses, calcium-forming micro-organisms and candida are part of our world. Unfortunately, so are toxic chemicals, including everything from pesticides to car pollution to nuclear radiation to most municipal tap waters. In our world these harmful micro-organisms and the endless list of toxic chemicals assault our immune system consistently. Coupled with these assaults are the daily stresses of life and their deleterious effects upon us.

All of these add up to a weakened immune system: colds and flus, coughs, fevers, chronic health problems, skin disorders, digestive distress, nervous conditions, chronic fatigue and even cancer. When the body has too much to deal with, it stops being able to get rid of its waste efficiently and requires more support to help it fight off what is attacking it.

Fortunately, our immune system can be improved and empowered to such a point that not only can the harmful microbes be halted and the chemicals detoxified, but also a “stress defense shield” may be built up that can even drive off the effects of daily stress.

We all can learn more about how to empower our own immunity. I believe the best way to activate genius within the immune system is by ingesting certain superherbs and superfoods, taking probiotics and cultured foods, minimizing toxic food exposure by eating pure, organic, raw-living foods and making appropriate healthy lifestyle improvements.

In 400 BC Hippocrates said, “Let food be your medicine and let medicine be your food.” Both aspects of this phrase must be considered - not just food as medicine, but also medicine as food - that means superfoods (the most nutrient-rich plant foods in the world) and tonic superherbs (herbs that can be taken regularly like food). Out of 40,000 herbs used worldwide, perhaps only 50-60 of them are tonic superherbs. These superherbs should be taken for long periods, because, like all tonics, they are more like food and they build health treasures within and nourish our “stress defense shield.”
Whenever possible, try to include the following superfoods, superherbs and super products in your daily regime:

1. Reishi Mushroom
Reishi is Queen of the Medicinal Mushrooms. Reishi is the most well-studied herb in the history of the world. She has been the most revered herbal mushroom in Asia for over 2,000 years. The Daoists consider Reishi an “elixir of immortality” that is celebrated for its ability to significantly improve the functioning of the immune system by protecting us from the onslaught of viruses, bacteria, unwanted guests, pollution, chemicals, molds, and the toxicity that we are often subjected to in our world. Reishi helps build up our “stress defense shield” creating feelings of well-being within in spite of outer stresses.

2. Chaga Mushroom
Chaga is the King of the Medicinal Mushrooms. It contains the highest amounts of anti-tumor compounds of any herb. These compounds are in the form of betulin, betulinic acid and lupeol, which are powerful anti-mutagenic compounds naturally present in the white part of the birch tree’s bark (in which the chaga typically grows). Chaga is also extremely high in nourishing phytochemicals, nutrients, and free-radical scavenging antioxidants, especially melanin. Chaga is second only to cacao in antioxidant content. Chaga is the most powerful cancer-fighting herb known.

3. Gynostemma
According to the scientific herbal research being conducted in the People’s Republic of China, gynostemma has been identified as the most medicinal of all the Chinese herbs. It contains 120 saponins (immune modulating molecules that are fat soluble on one side of the molecule and water soluble on the other side) - all of which possess unique and specific health-giving properties. Gynostemma is a true tonic - you can take it or make tea out of it nearly every day with benefits that accrue the more you consume it. Gypenoside 49 (49th of the 120 saponins) has been identified as a telomerase activator that youthens us genetically.

4. Ginseng
Known throughout the world for its amazing energy-restoring and strength-building properties, ginseng is an adaptogen that helps our bodies “adapt” to stressful environmental conditions. Ginseng root can boost energy, induce mental alertness and increase endurance. Ginseng also helps fight pain and alleviate radiation damage to healthy tissues.

5. Chlorella
Chlorella is a natural green micro-algae, and a superfood detoxifier. It contains high levels of complete protein with properties that bond with heavy metals and chemical toxins, helping to eliminate them from the brain and nervous system. Chlorella is the highest chlorophyll-containing plant in the world with 40 times the chlorophyll content of the best wheatgrass juice known.

6. Zeolites
Zeolites are a form of unique, volcanic mineral compounds with crystalline structures that form a sort of “cage.” This “cage” works like a magnet to attract heavy metals, chemicals and other pollutants (e.g. radioactive isotopes), capturing them and allowing their easy removal (without being re-absorbed) from the body. Zeolites have been shown to have anti-viral and cancer-fighting effects.

7. Shilajit
Contains 80+ minerals and fulvic acid which assists in the removal of toxins, improves nutrition to cells and helps restore electricity to the blood. Shilajit promotes the movement of minerals into muscle, tissue and bone. It is an Ayurvedic mineral-herb which translates as the “conqueror of mountains and destroyer of weakness.”

8. Astragalus Root
One of the most potent immune tonics used to improve the lungs, strengthen muscles, increase metabolism, reduce stress and strengthen the genetics. The first telomerase activator product to make it into the market is TA-65, an extract of astragalus.

9. Camu Camu Berry
This plant-derived Vitamin C source will super-boost your immune system and help repair connective tissue. Camu Camu is one of the most concentrated supplies of Vitamin C in the world, and a powerful antioxidant.

10. Probiotics
Consuming a combination of good quality probiotics (these include friendly bacteria such as: Lactobacillus acidophilus, Bifidus infantis, B. longum, L. bulgaricus, S. thermophilus, L. plantarum, L. salivarius, Enterococcus faecium, etc.) and cultured and fermented foods like coconut kefir will lead to enhanced immunity as the beneficial probiotic bacteria are symbiotic allies to your body that help: fight viruses, candida and other infections; produce B vitamins; and assist in detoxification. Probiotics help build up that “stress defense shield.”

We live in a time of unprecedented abundance. Through the Internet and the advancing health freedoms we are all enjoying, we have easy access to these superfoods, superherbs and super health products.
When you start investigating and utilizing these substances consistently and regularly, you will notice that your immunity will step-by-step be enhanced. Your thoughts will have more clarity. Your overall energy will increase. You will also likely sleep better and perform better in athletic activities. Your overall productivity will improve. Digestive distress decreases. Feelings of well-being begin to dominate your life.

Superfoods and tonic superherbs can be added into anyone’s diet. Simply begin with the first one or few that you’re drawn to and go from there. Get out a blender and have fun. Make different teas with the superherbs or smoothies with the superfoods. Better yet, take your superherb tea and blend it with your superfoods to make the best elixirs ever. Getting healthier and healthier is fun!

Source: www.life.gaiam.com

Saturday, July 11, 2015

The Vague Nerve
- a single nerve that connects all of your vital organs - and it might just be the future of medicine

When Maria Vrind, a former gymnast from Volendam in the Netherlands, found that the only way she could put her socks on in the morning was to lie on her back with her feet in the air, she had to accept that things had reached a crisis point.
“I had become so stiff I couldn’t stand up,” she says. “It was a great shock because I’m such an active person.”
It was 1993. Vrind was in her late 40s and working two jobs, athletics coach and a carer for disabled people, but her condition now began taking over her life. “I had to stop my jobs and look for another one as I became increasingly disabled myself.” By the time she was diagnosed, seven years later, she was in severe pain and couldn’t walk any more. Her knees, ankles, wrists, elbows and shoulder joints were hot and inflamed. It was rheumatoid arthritis, a common but incurable autoimmune disorder in which the body attacks its own cells, in this case the lining of the joints, producing chronic inflammation and bone deformity.

Waiting rooms outside rheumatoid arthritis clinics used to be full of people in wheelchairs. That doesn’t happen as much now because of a new wave of drugs called biopharmaceuticals – such as highly targeted, genetically engineered proteins – which can really help. Not everyone feels better, however: even in countries with the best healthcare, at least 50 per cent of patients continue to suffer symptoms.

Like many patients, Vrind was given several different medications, including painkillers, a cancer drug called methotrexate to dampen her entire immune system, and biopharmaceuticals to block the production of specific inflammatory proteins. The drugs did their job well enough – at least, they did until one day in 2011, when they stopped working.

“I was on holiday with my family and my arthritis suddenly became terrible and I couldn’t walk – my daughter-in-law had to wash me.” Vrind was rushed to hospital, where she was hooked up to an intravenous drip and given another cancer drug, one that targeted her white blood cells. “It helped,” she admits, but she was nervous about relying on such a drug long-term.

Luckily, she would not have to. As she was resigning herself to a life of disability and monthly chemotherapy, a new treatment was being developed that would profoundly challenge our understanding of how the brain and body interact to control the immune system. It would open up a whole new approach to treating rheumatoid arthritis and other autoimmune diseases, using the nervous system to modify inflammation. It would even lead to research into how we might use our minds to stave off disease.
"A new treatment was being developed that would lead to research into how we might use our minds to stave off disease."
And, like many good ideas, it came from an unexpected source.

The nerve hunter

Kevin Tracey, a neurosurgeon based in New York, is a man haunted by personal events – a man with a mission. “My mother died from a brain tumour when I was five years old. It was very sudden and unexpected,” he says. “And I learned from that experience that the brain – nerves – are responsible for health.”

This drove his decision to become a brain surgeon. Then, during his hospital training, he was looking after a patient with serious burns who suddenly suffered severe inflammation. “She was an 11-month-old baby girl called Janice who died in my arms.” 
These traumatic moments made him a neurosurgeon who thinks a lot about inflammation. He believes it was this perspective that enabled him to interpret the results of an accidental experiment in a new way.

In the late 1990s, Tracey was experimenting with a rat’s brain. “We’d injected an anti-inflammatory drug into the brain because we were studying the beneficial effect of blocking inflammation during a stroke,” he recalls. “We were surprised to find that when the drug was present in the brain, it also blocked inflammation in the spleen and in other organs in the rest of the body. Yet the amount of drug we’d injected was far too small to have got into the bloodstream and travelled to the rest of the body.”

After months puzzling over this, he finally hit upon the idea that the brain might be using the nervous system – specifically the vagus nerve – to tell the spleen to switch off inflammation everywhere.
It was an extraordinary idea – if Tracey was right, inflammation in body tissues was being directly regulated by the brain.
"If Tracey was right, inflammation in body tissues was being directly regulated by the brain."
Communication between the immune system’s specialist cells in our organs and bloodstream and the electrical connections of the nervous system had been considered impossible. Now Tracey was apparently discovering that the two systems were intricately linked.
The first critical test of this exciting hypothesis was to cut the vagus nerve.
When Tracey and his team did, injecting the anti-inflammatory drug into the brain no longer had an effect on the rest of the body. The second test was to stimulate the nerve without any drug in the system.

“Because the vagus nerve, like all nerves, communicates information through electrical signals, it meant that we should be able to replicate the experiment by putting a nerve stimulator on the vagus nerve in the brainstem to block inflammation in the spleen,” he explains. “That’s what we did and that was the breakthrough experiment.”

The wandering nerve

The vagus nerve starts in the brainstem, just behind the ears.
It travels down each side of the neck, across the chest and down through the abdomen. ‘Vagus’ is Latin for ‘wandering’ and indeed this bundle of nerve fibres roves through the body, networking the brain with the stomach and digestive tract, the lungs, heart, spleen, intestines, liver and kidneys, not to mention a range of other nerves that are involved in speech, eye contact, facial expressions and even your ability to tune in to other people’s voices. 

It is made of thousands and thousands of fibres and 80 per cent of them are sensory, meaning that the vagus nerve reports back to your brain what is going on in your organs.
Operating far below the level of our conscious minds, the vagus nerve is vital for keeping our bodies healthy. It is an essential part of the parasympathetic nervous system, which is responsible for calming organs after the stressed ‘fight-or-flight’ adrenaline response to danger. Not all vagus nerves are the same, however: some people have stronger vagus activity, which means their bodies can relax faster after a stress.

The strength of your vagus response is known as your vagal tone and it can be determined by using an electrocardiogram to measure heart rate. Every time you breathe in, your heart beats faster in order to speed the flow of oxygenated blood around your body. Breathe out and your heart rate slows. This variability is one of many things regulated by the vagus nerve, which is active when you breathe out but suppressed when you breathe in, so the bigger your difference in heart rate when breathing in and out, the higher your vagal tone.

Research shows that a high vagal tone makes your body better at regulating blood glucose levels, reducing the likelihood of diabetes, stroke and cardiovascular disease. Low vagal tone, however, has been associated with chronic inflammation.

As part of the immune system, inflammation has a useful role helping the body to heal after an injury, for example, but it can damage organs and blood vessels if it persists when it is not needed. One of the vagus nerve’s jobs is to reset the immune system and switch off production of proteins that fuel inflammation. Low vagal tone means this regulation is less effective and inflammation can become excessive, such as in Maria Vrind’s rheumatoid arthritis or in toxic shock syndrome, which Kevin Tracey believes killed little Janice.

Having found evidence of a role for the vagus in a range of chronic inflammatory diseases, including rheumatoid arthritis, Tracey and his colleagues wanted to see if it could become a possible route for treatment. The vagus nerve works as a two-way messenger, passing electrochemical signals between the organs and the brain.
The vagus nerve works as a two-way messenger, passing electrochemical signals between the organs and the brain.
In chronic inflammatory disease, Tracey figured, messages from the brain telling the spleen to switch off production of a particular inflammatory protein, tumour necrosis factor (TNF), weren’t being sent. Perhaps the signals could be boosted?
He spent the next decade meticulously mapping all the neural pathways involved in regulating TNF, from the brainstem to the mitochondria inside all our cells.
Eventually, with a robust understanding of how the vagus nerve controlled inflammation, Tracey was ready to test whether it was possible to intervene in human disease.

Stimulating trial

In the summer of 2011, Maria Vrind saw a newspaper advertisement calling for people with severe rheumatoid arthritis to volunteer for a clinical trial. Taking part would involve being fitted with an electrical implant directly connected to the vagus nerve. “I called them immediately,” she says. “I didn’t want to be on anticancer drugs my whole life; it’s bad for your organs and not good long-term.”

Tracey had designed the trial with his collaborator, Paul-Peter Tak, professor of rheumatology at the University of Amsterdam. Tak had long been searching for an alternative to strong drugs that suppress the immune system to treat rheumatoid arthritis. “The body’s immune response only becomes a problem when it attacks your own body rather than alien cells, or when it is chronic,” he reasoned. “So the question becomes: how can we enhance the body’s switch-off mechanism? How can we drive resolution?”

When Tracey called him to suggest stimulating the vagus nerve might be the answer by switching off production of TNF, Tak quickly saw the potential and was enthusiastic to see if it would work. Vagal nerve stimulation had already been approved in humans for epilepsy, so getting approval for an arthritis trial would be relatively straightforward. A more serious potential hurdle was whether people used to taking drugs for their condition would be willing to undergo an operation to implant a device inside their body: “There was a big question mark about whether patients would accept a neuroelectric device like a pacemaker,” Tak says.

He needn’t have worried. More than a thousand people expressed interest in the procedure, far more than were needed for the trial. In November 2011, Vrind was the first of 20 Dutch patients to be operated on.

“They put the pacemaker on the left-hand side of my chest, with wires that go up and attach to the vagus nerve in my throat,” she says. “I waited two weeks while the area healed, and then the doctors switched it on and adjusted the settings for me.”

She was given a magnet to swipe across her throat six times a day, activating the implant and stimulating her vagus nerve for 30 seconds at a time. The hope was that this would reduce the inflammatory response in her spleen. As Vrind and the other trial participants were sent home, it became a waiting game for Tracey, Tak and the team to see if the theory, lab studies and animal trials would bear fruit in real patients. “We hoped that for some, there would be an easing of their symptoms – perhaps their joints would become a little less painful,” Tak says.
At first, Vrind was a bit too eager for a miracle cure. She immediately stopped taking her pills, but her symptoms came back so badly that she was bedridden and in terrible pain. She went back on the drugs and they were gradually reduced over a week instead.
And then the extraordinary happened: Vrind experienced a recovery more remarkable than she or the scientists had dared hope for.
The extraordinary happened: Vrind experienced a recovery more remarkable than she or the scientists had dared hope for.
“Within a few weeks, I was in a great condition,” she says. “I could walk again and cycle, I started ice-skating again and got back to my gymnastics. I feel so much better.”
She is still taking methotrexate, which she will need at a low dose for the rest of her life, but at 68, semi-retired Vrind now plays and teaches seniors’ volleyball a couple of hours a week, cycles for at least an hour every day, does gymnastics, and plays with her eight grandchildren.

Other patients on the trial had similar transformative experiences. The results are still being prepared for publication but Tak says more than half of the patients showed significant improvement and around one-third are in remission – in effect cured of their rheumatoid arthritis. Sixteen of the 20 patients on the trial not only felt better, but measures of inflammation in their blood also went down. Some are now entirely drug-free. Even those who have not experienced clinically significant improvements with the implant insist it helps them; nobody wants it removed.

“We have shown very clear trends with stimulation of three minutes a day,” Tak says. “When we discontinued stimulation, you could see disease came back again and levels of TNF in the blood went up. We restarted stimulation, and it normalised again.”

Tak suspects that patients will continue to need vagal nerve stimulation for life. But unlike the drugs, which work by preventing production of immune cells and proteins such as TNF, vagal nerve stimulation seems to restore the body’s natural balance. It reduces the over-production of TNF that causes chronic inflammation but does not affect healthy immune function, so the body can respond normally to infection.

“I’m really glad I got into the trial,” says Vrind. “It’s been more than three years now since the implant and my symptoms haven’t returned. At first I felt a pain in my head and throat when I used it, but within a couple of days, it stopped. Now I don’t feel anything except a tightness in my throat and my voice trembles while it’s working.

“I have occasional stiffness or a little pain in my knee sometimes but it’s gone in a couple of hours. I don’t have any side-effects from the implant, like I had with the drugs, and the effect is not wearing off, like it did with the drugs.”

Raising the tone

Having an electrical device surgically implanted into your neck for the rest of your life is a serious procedure. But the technique has proved so successful – and so appealing to patients – that other researchers are now looking into using vagal nerve stimulation for a range of other chronic debilitating conditions, including inflammatory bowel disease, asthma, diabetes, chronic fatigue syndrome and obesity.

But what about people who just have low vagal tone, whose physical and mental health could benefit from giving it a boost? Low vagal tone is associated with a range of health risks, whereas people with high vagal tone are not just healthier, they’re also socially and psychologically stronger – better able to concentrate and remember things, happier and less likely to be depressed, more empathetic and more likely to have close friendships.

Twin studies show that to a certain extent, vagal tone is genetically predetermined – some people are born luckier than others. But low vagal tone is more prevalent in those with certain lifestyles – people who do little exercise, for example. This led psychologists at the University of North Carolina at Chapel Hill to wonder if the relationship between vagal tone and wellbeing could be harnessed without the need for implants.

In 2010, Barbara Fredrickson and Bethany Kok recruited around 70 university staff members for an experiment. Each volunteer was asked to record the strength of emotions they felt every day. Vagal tone was measured at the beginning of the experiment and at the end, nine weeks later. As part of the experiment, half of the participants were taught a meditation technique to promote feelings of goodwill towards themselves and others. 

Those who meditated showed a significant rise in vagal tone, which was associated with reported increases in positive emotions. “That was the first experimental evidence that if you increased positive emotions and that led to increased social closeness, then vagal tone changed,” Kok says.
Now at the Max Planck Institute in Germany, Kok is conducting a much larger trial to see if the results they found can be replicated. If so, vagal tone could one day be used as a diagnostic tool. In a way, it already is. “Hospitals already track heart-rate variability – vagal tone – in patients that have had a heart attack,” she says, “because it is known that having low variability is a risk factor.”
The implications of being able to simply and cheaply improve vagal tone, and so relieve major public health burdens such as cardiovascular conditions and diabetes, are enormous. It has the potential to completely change how we view disease.
It has the potential to completely change how we view disease.
If visiting your GP involved a check on your vagal tone as easily as we test blood pressure, for example, you could be prescribed therapies to improve it. But this is still a long way off: “We don’t even know yet what a healthy vagal tone looks like,” cautions Kok. “We’re just looking at ranges, we don’t have precise measurements like we do for blood pressure.” 
What seems more likely in the shorter term is that devices will be implanted for many diseases that today are treated by drugs: “As the technology improves and these devices get smaller and more precise,” says Kevin Tracey, “I envisage a time where devices to control neural circuits for bioelectronic medicine will be injected – they will be placed either under local anaesthesia or under mild sedation.”

However the technology develops, our understanding of how the body manages disease has changed for ever. “It’s become increasingly clear that we can’t see organ systems in isolation, like we did in the past,” says Paul-Peter Tak. “We just looked at the immune system and therefore we have medicines that target the immune system.

“But it’s very clear that the human is one entity: mind and body are one. It sounds logical but it’s not how we looked at it before. We didn’t have the science to agree with what may seem intuitive. Now we have new data and new insights.”

And Maria Vrind, who despite severe rheumatoid arthritis can now cycle pain-free around Volendam, has a new lease of life: “It’s not a miracle – they told me how it works through electrical impulses – but it feels magical. I don’t want them to remove it ever. I have my life back!”

Source: www.businessinsider.com