Welcome to Delicate template
Header
Just another WordPress site
Header

Exposure to chronic constant emotional or physical stress triggers a vicious cycle of inflammation. The stress increases the amount of inflammation that the body generates, and the additional inflammation “feeds” more stress.

Depressed individuals report that they experience high levels of tension and anxiety, fatigue, muscle discomfort, and/or gastrointestinal problems. Often they have a feeling that “something is very wrong”, but they cannot pinpoint what is bothering them.

Individuals suffering from depression often start by visiting physicians that specialize in specific organ systems of the body. For example a neurologist (specialty in the nerves), a gastroenterologist (digestive system), or a psychiatrist (medical doctor) or a psychologist, practitioners specializing in mental disorders. Unfortunately, most of these experts tend to focus on a single part of the body.

Since the human body is a single organism, and all the organ systems are integrated, it might be useful to realize that there is substantial and constant cross talk between all the organ systems of the body. Affect one part of the body and it has a ripple effect on all the other parts of the body.

As an example, when individuals are depressed, their immune cells produce large amounts of inflammatory molecules, pro-inflammatory cytokines, which circulate throughout the body. Since cytokines act in a hormone-like fashion, they affect all parts of the body and the brain.

Treatment Resistant Depression
Over seven million individuals with depression find little or no relief that prescribed antidepressant medications. A significant number of these patients have high levels of inflammatory cytokines, immune messages that result in inflammation. These inflammatory cytokines can interfere with the actions of medications.
Lifestyle Changes.

Too many individuals are convinced that only prescription medications can make a difference in their depression and anxiety. However, there are certain life style changes that may help them, with their clinician’s approval, decrease their medication.*

(*Note: The following lifestyle changes should only be incorporated after consultation with a qualified health practitioner. If you are on prescription medications, especially for depression or anxiety, DO NOT REDUCE OR STOP ANY MEDICATIONS without consulting with the prescribing health practitioner.)

Some naturally oriented steps that one can take are:

EXERCISE:
Researchers at Duke University Medical Center, Durham, NC, found that a brisk 30-minute walk or jog three times a week may be just as effective in relieving major depression as are antidepressant prescription medications. Patients were assigned to three groups: antidepressant medications only, exercise only, or a combination of both medication and exercise. The scientists found that the exercise by itself was just as effective as medication and “was equally effective in reducing depression…” as were antidepressants.

One reason exercise may be so effective in reducing the inflammatory-depression cycle is that every time a muscle contracts, it releases anti-inflammatory immune cytokines that reduce inflammation and a help to decrease anxiety, and improve mood.
SUNSHINE AND FRESH AIR:
The amount of time subjects are exposed to sunlight is directly related to the amount of a specific inflammatory cytokine they produce, and depressed individuals show differing levels of the cytokine when exposed to light for varying amounts of time.
Moderate exposure to sunshine and fresh air may contribute greatly to feeling less depressed. This may “simply” be because when one is exposed to sunlight, vitamin D is produced by the body.

Vitamin D is more like a “hormone” than a purely nutritional element, since it affects hundreds of genes and is a powerful immune system regulator. Although still not definitively proven, individuals living in temperate areas may find that taking vitamin D3 supplements may prove helpful.

EAT SMARTER:
Increase the amount of fresh and colorful fruits and vegetables, beans, fish, and chicken. Limit non-nutritious “foods”, especially fried foods, sweets, sodas (diet or regular!), white rice, and pasta. Eating in a nutritional manner may help the body regulate its daily inflammatory responses.

CONTROL YOUR WEIGHT:
Fat cells, adipose cells, especially those around abdomen produce a wide range of inflammatory cytokines. As the size of the cells decrease, the amount of inflammation that the body produces decreases. Lowering inflammation helps an individual to return to their natural immune homeostasis, their natural immune balance.

OMEGA-3 FATTY ACIDS FROM FISH OILS:
Studies suggest that daily consumption of omega-3 fatty acids from fish makes a difference in depression. In a recent randomized double-blind placebo-controlled study of shift workers, supplementation with omega-3 was associated with a reduction in high sensitivity C-reactive protein (an inflammatory marker) and depression. In another study of women, the highest intake of omega-3 was associated with a 49% decrease in symptoms of depression. In the latter study, investigators suggested that omega-3 was triggering the production of anti-inflammatory compounds.

RETURN THE BODY TO IMMUNE BALANCE, IMMUNE HOMEOSTASIS:
Inflammation in the body is a normal and desired process that is part of the healing cycle and it is the primary method by which the body defends itself from pathogens. The key to good health is to help the body achieve the right level of inflammation, immune homeostasis. We want the body to produce enough of an inflammatory response to defend itself from pathogens and cancerous cells, but not so much inflammation that healthy tissues are damaged.

Hyperimmune egg has been shown to help the body return to immune homeostasis, immune balance. In a university, double-blind placebo-controlled trial (the gold standard of human trials), subjects consuming hyperimmune egg reported lower levels of moodiness, anger, and hostility. [Med Sci Sports Exer 2009 5:228].

SUMMARY
Chronic inflammation, brought about by an over-expression or lack of control of the normal protective mechanisms of the body, has been linked to range of conditions including depression.
Individuals who control inflammatory responses will have a much higher emotional and physical quality of life.

www.ncbi.nlm.nih.gov/pubmed/15694227
www.ncbi.nlm.nih.gov/pubmed/23873713
www.karger.com/Article/Fulltext/51732
www.ncbi.nlm.nih.gov/pubmed/20609377
www.ncbi.nlm.nih.gov/pubmed/15694227
www.ncbi.nlm.nih.gov/pubmed/19423079
www.ncbi.nlm.nih.gov/pubmed/18580840
www.ncbi.nlm.nih.gov/pubmed/20600462
www.ncbi.nlm.nih.gov/pubmed/10547175
www.ncbi.nlm.nih.gov/pubmed/23497121
www.ncbi.nlm.nih.gov/pubmed/14696037
www.ncbi.nlm.nih.gov/pubmed/24005610
bit.ly/1enpcdi
www.ncbi.nlm.nih.gov/pubmed/23874068
www.ncbi.nlm.nih.gov/pubmed/24005610
www.psychiatrictimes.com/depression/inflammation-and-treatment-resistance-major-depression-perfect-storm

Shirley Wang published an article in the WSJ titled “New View of Depression: An Ailment of the Entire Body”. Her lead-in stated: “Scientists are increasingly finding that depression and other psychological disorders can be as much diseases of the body as of the mind. People with long-term psychological stress, depression and post-traumatic stress disorder tend to develop earlier and more serious forms of physical illnesses that usually hit people in older age, such as stroke, dementia, heart disease and diabetes”.

Ms. Wang reported that Dr. Owen Wolkowitz at the University of California, San Francisco thinks of depression as “a systemic illness”, rather than a mental or brain disease. Dr. Wolkowitz found that
“[D]epression is associated with an unusually high rate of aging-related illnesses and early mortality”, or “accelerated aging”. He also points out that individuals who are aging more rapidly and/or are ill, have shorter telomeres than expected.

[Division is essential for most healthy cells. Telomeres are the protective tips of chromosomes that guide the chromosomes during cell division. Every time a cell divides, the telomeres shorten in length. Eventually there is little or no telomere resulting in an inability of the cell to divide efficiently. Eventually the cell dies. Some investigators are of the opinion that the length of telomeres is a predictor of longevity.]

There appears to be a strong association of inflammation with shorter telomeres. Senescent cells, which are unable to divide any longer and have almost non-existent telomeres, produce high concentrations of immune factors, cytokines, that regulate genes that result in inflammation.

Chronic inflammation is found in a myriad of diseases including cardiovascular disease, stroke, diabetes, cancer multiple sclerosis, dementia, as well as depression. Heightened levels of inflammation are found in smokers and the obese. Each pack of cigarettes smoked results in a 18% shortening of telomeres, and the telomeres of obese women are shorter than those of lean women. Using other biomarkers, both smokers and obese individuals have higher levels of inflammation in their bodies than the general population.

Depression results in inflammation and inflammation “feeds” depression. The same cytokines that cause inflammation, pro-inflammatory cytokines, under other circumstances may be anti-inflammatory.
Data from studies demonstrate that depressed individuals have an imbalance of pro- and anti-inflammatory factors.

Some practitioners suggest that depressed patients need to “boost” their immune responses. Instead, “boosting” the immune response, i.e., inflammation, may only exacerbate the disease.

Because of the complexity of immune responses, it is important to let the body find its own “set” point. This is why achieving immune homeostasis, immune balance, is essential for good health.

http://twinsuk.ac.uk/wp-content/uploads/2012/03/Valdes-.lancet.pdf
http://www.ncbi.nlm.nih.gov/pubmed/23136552
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1868538/
http://www.ncbi.nlm.nih.gov/pubmed/17705097
http://www.sciencedirect.com/science/article/pii/S0022395609001241
http://drhellengreenblatt.info/2011/09/smoking-inflammation-immune-homeostasis-balance/

Immune inflammation is the body’s way of protecting itself from infection and cancerous cells. It is also necessary for repairing damaged tissues and eliminating dangerous compounds produced internally or to which we are exposed to externally.

In the 1800’s, Dr. Rudolf Virchow, one of the 19th century’s foremost scientists, observed the presence of inflammatory immune cells in cancerous tissues and suggested that there was a connection between cancer and inflammation.

The right balance of inflammatory responses are needed to fight cancer. Too little of an immune response leaves cancer cells unrecognized and unchallenged. Too much inflammation, or going down a different pathway of immune cell stimulation, may cause the immune system to support tumor growth rather than go into an “attack” mode.

Immune and digestive homeostasis, intestinal balance, depends on the right types and numbers of microbiota (bacteria), the health of the cells that make up the intestinal lining, and the immune cells that are embedded in the intestinal walls.

Over 75-80% of the immune system is represented in the gut. The immune cells produce antibodies (immunoglobulins), cytokines, and other immune factors that help protect the digestive system from pathogens that are introduced into the gut when consuming food and drink.

Bacteria and their secretions interact with intestinal immune cells and vice versa. These bacteria play a major role in the health of the digestive tract. An inappropriate level of intestinal immune responsiveness and incorrect types and numbers of microbiota may contribute to difficulty in maintaining intestinal homeostasis, gut balance. Immune imbalances, a breakdown of any of these elements, lead to problems with the intestine such as inflammatory bowel disease or cancer.

Pre-cancerous polyps often precede the development of colorectal cancer. Several naturally occurring substances have been shown to reduce the size and number of polyps, probably by down-regulation of genes that cause inflammation.

Maintaining immune and digestive homeostasis is imperative for good health. I look forward to having you contact me about any questions you might have on limiting inflammation and returning to homeostasis. I can be contacted at: DrHellen@DrHellenGreenblatt.info or click on: http://drhellengreenblatt.info/contact-dr-hellen/. You may also reach me at: 1.302-265.3870 [USA, Eastern Time].

www.nature.com/nature/journal/v454/n7203/abs/nature07201.html
serpins.med.unc.edu/~fcc/Biology134_Folder/Pathology_213/Inflamm-Cancer.pdf
www.ncbi.nlm.nih.gov/pubmed/22893204
www.ncbi.nlm.nih.gov/pmc/articles/PMC2916138/
www.ncbi.nlm.nih.gov/pubmed/21677746

People often ask how they ended up getting an autoimmune disease, a condition in which their own immune system turns on themselves and destroys healthy by-stander tissues and organs.

My response-the not-yet-proven-hypothesis that molecular mimicry results in autoimmune disease.

Molecular mimicry is a phenomenon in which tissues in the body share a “barcode”, antigenic receptors,  with specific viruses or a bacteria.  The immune system responds by mounting an inflammatory attack against the invading pathogen.  This response targets not only the pathogen, but in addition, tissues that share the same antigenic makeup as the invading microorganism. In short, a terrible error occurs and the body starts destroying itself.

The inflammatory disease rheumatic fever is an excellent example of the possible outcome of molecular mimicry. Damage of heart valves may occur after infection with the bacteria Streptococcus. This development accounts for the panic that many parents experience when their kids come down with “strep throat”.

Antibodies, large unique proteins,  are produced by the immune system when the body is exposed to pathogens.  These specialized proteins attach to the invaders, “flagging” them for destruction by circulating immune cells.  In the case of rheumatic fever, since bacteria and heart valve tissue look alike to the body, antibodies are produced that attach to both surfaces, triggering inflammatory immune responses ultimately resulting in damage to heart valves, as well as death of the bacteria.

The data, controversial, but compelling, is that molecular mimicry, due to viral and bacterial infections,  may also be a trigger for neurological disease.

This concept is reinforced by the fact that multiple sclerosis is a condition in which nerve cells are damaged by uncontrolled levels of inflammation.  Immune cell products mistakenly attack myelin proteins, which make up the protective sheath that “insulates” nerves.  Damage to this covering results in nerve signals becoming intermittent, slowing down, or stopping entirely.  Such nerve damage affects vision, mobility, coordination, balance, bladder, or bowel control.

 A large body of data suggests that infection with herpes virus 6 and/or Epstein-Barr virus triggers  inflammation that leads to nerve cell destruction.  Different viruses and bacteria have been implicated as initiating inflammatory responses in other neurodegenerative diseases as well.

 To understand the role of excessive inflammation in your own condition, enter the condition in combination with the word “inflammation”.  The results you receive will help you understand the importance of achieving immune homeostasis, immune balance of our inflammatory responses.

Let me help you improve your quality of life, naturally. Please contact me at 302.265.3870 (USA ET) or email: DrHellen@DrHellenGreenblatt.info

http://www.bjmp.org/content/role-chronic-bacterial-and-viral-infections-neurodegenerative-neurobehavioral-psychiatric-au
http://www.ncbi.nlm.nih.gov/pubmed/22617826
http://www.ncbi.nlm.nih.gov/pubmed/18193392
http://www.ncbi.nlm.nih.gov/pubmed/9761770
http://www.ncbi.nlm.nih.gov/pubmed/22201827
http://www.ncbi.nlm.nih.gov/pubmed/12557285
http://www.ncbi.nlm.nih.gov/pubmed/21859892

A healthy immune system controls the amount of inflammation the body uses to defend itself from infection and mutating cancer cells, and to help its healing processes. The body has to control the intensity of its inflammatory responses so that it doesn’t attack healthy, “by-stander” cells and tissues.  [When the body attacks its own self, an autoimmune response, conditions such as arthritis, lupus, and diabetes result.]  To control inflammation means that the body has to stay balanced all the time.  When inflammatory responses are balanced the body is in immune/inflammatory homeostasis.

Immune homeostasis, immune balance is what keeps cancer in check.  Too much inflammation may trigger cancer cells to grow and multiply, and they in turn may trigger more inflammation to occur. 

 Cigarette smoke has carcinogens, compounds, that cause genes to mutate, or to switch on and off, phenomena known as epigenic events.  Additionally, exposure to cigarette smoke stimulates the release of inflammatory cytokines, molecular messages produced by immune cells.  When these molecules are released into the body they may cause imbalances in the inflammatory process, and a loss of immune homeostasis, immune balance.

Smoking results in the perfect “cancer storm”, because cigarette smoke not only cause inflammation, but it also contributes to angiogensis, the growth of new blood vessels that tumor cells use to grow and multiply in numbers.

 Normally, there is a balance of growth-stimulating and growth-inhibitory molecules so that blood vessels form only when and where they are needed, for example when blood vessels are damaged. 

However, cancer cells upset signaling and the body starts produces fresh blood vessels. These blood vessels “feed” growing tumors with oxygen and nutrients, allowing the cancer cells to invade nearby tissues and to migrate throughout the body, metastasizing, and forming new colonies of cancer cells.

 A study from the National Cancer Institute published this month, analyzed 1400 different inflammatory and immune genes from lung cancer patients and healthy individuals.  In 44 genes there appeared to be an association between lung cancer and certain genetic differences in the cells.

 The scientists focused their work on an important inflammatory gene and found that individuals with a specific type of gene linked to inflammation had a 21% to 44% lower likelihood of getting lung cancer than those with a different form of the same gene.

 Once again, the key is that the body needs to stay in balance, and if you maintain balance, especially  immune inflammatory homeostasis, your quality of life will be changed forever.

 Feel free to contact Dr. Hellen at DrHellen@DrHellenGreenblatt.info with questions or to consult with her.  A message may also be left at: 1.302-265.3870 or click on: http://drhellengreenblatt.info/contact-dr-hellen/.

 
http://www.cancer.gov/cancertopics/factsheet/Therapy/angiogenesis-inhibitors
http://www.ncbi.nlm.nih.gov/pubmed/21751938
http://www.freep.com/article/20121008/FEATURES08/121008047/Scientists-link-gene-to-lower-risk-of-lung-cancer?odyssey=nav%7Chead
http://www.news-medical.net/news/20121008/NFKB1-gene-variant-may-reduce-risk-of-lung-cancer.aspx

Gut-associated lymphoid tissues are found in the walls of the intestine and contain billions of immune cells.  The white blood cells control the levels and types of bacteria that naturally populate the intestines.  The bacteria help to digest food that provides energy to the body,  and are part of the immune/bacterial ecosystem of the intestine.

 Interestingly, both immune cells and bacteria, protect the intestines from attack by pathogenic microorganisms, and cancer cells, and help heal the intestines when they are damaged.  Cross talk between the bacteria, and immune cells help the intestines maintain homeostasis, balance.  Each keeps the other in check.

 CELIAC DISEASE
Celiac disease is an intestinal, inflammatory, autoimmune (against oneself) disorder.  Individuals with celiac disease suffer from a wide-range of symptoms including diarrhea, fatigue, weight loss, inability to focus, skin and neurological issues, constipation, a feeling of being “bloated”, gas, anemia, headaches, osteoporosis (loss of bone density), and depression. 

 Ingesting grains, such as wheat, rye, and barley, which contain a component of protein called gluten, reportedly stimulate celiac disease.

 The presence of gluten stimulates sensitive immune cells to produce proinflammatory cytokines.  These immune messages drive inflammation, resulting in the destruction of the intestinal wall and symptoms.   Genetic, environmental, dietary, neuroendocrine, and immunological factors all contribute to disease progression.

 Currently, the primary guidance that celiacs get, is to go on a “gluten-free” diet.  Although it may be effective for some people,  such diets are restrictive, expensive, and do not work well for everyone.  In one study, every patient, 100% of those surveyed, in a cohort of 300 individuals, hoped for another option.

 OTHER APPROACHES
I often hear from people with autoimmune challenges such as celiac disease, “it’s genetic”.  Fine, so your genes are partially to blame. Meanwhile, what will you do? Continue to be uncomfortable?  So I ask those with inflammatory issues, why not consider short-term approaches until researchers discover longer-term solutions?  In three words: limit excessive inflammation.

 I like to describe inflammation as a way that the body “burns” out pathogenic microorganisms and cancer cells. The body must produce enough inflammation to protect itself from disease, and help the healing process, but not so much that healthy tissue, for example the intestinal lining, is damaged.

 Nutritional Approaches
Vitamin C and omega-3 fatty acids, from fish oil, inhibit the production of proinflammatory cytokines. (There is however,  evidence that vitamin A increases inflammatory processes.).

 Medical Approaches
Antibodies against specific inflammatory cytokines reduce intestinal injury in celiac disease, and the administration of corticosteroids, along with a gluten-free diet, was reported, in a small clinical trial, to provide benefit to celiac patients.

 Immunological Homeostasis/Balance
Hyperimmune egg, an ingredient that helps the body return to immunological balance, helps to support gastrointestinal health.  Many individuals with digestive issues report daily consumption of hyperimmune egg leads to major differences in their quality of life.

 LIMIT INFLAMMATION FOR BETTER HEALTH
The key to a higher level of quality of life in celiac and other autoimmune and autoinflammatory conditions, is to help the body limit its excessive inflammatory responses.  Removing gluten from one’s diet, using vitamin C, omega-3, corticosteroids, and hyperimmune egg, may contribute to helping the body regulate run-away inflammation.

Feel free to contact Dr. Hellen at DrHellen@DrHellenGreenblatt.info with questions or to consult with her. A message may also be left at: 1.302-265.3870 or click on: http://drhellengreenblatt.info/contact-dr-hellen/.


www.cell.com/cell-host-microbe/retrieve/pii/S1931312812000662

 www.medscape.com
 www.nature.com/nature/journal/v471/n7337/full/nature09849.html
www.nature.com/nature/journal/v471/n7337/full/nature09849.html
www.nature.com/nature/journal/v474/n7351/full/nature10208.html
www.ncbi.nlm.nih.gov/pubmed/18667914
www.ncbi.nlm.nih.gov/pubmed/22024540
www.ncbi.nlm.nih.gov/pubmed/22109896
www.ncbi.nlm.nih.gov/pubmed/22606367
www.ncbi.nlm.nih.gov/pubmed?term=morningstar%20hyperimmune%20egg
 www.sciencedaily.com/releases/2008/11/081114185942.htm
www.sciencedaily.com/releases/2012/04/120426105654.htm

 

Alzheimer’s and IVIG Rx
Last week John Gever, Senior Editor, MedPage Today brought attention to the results of a small study presented at the 2012 Alzheimer’s Association International Conference held in Vancouver, British Columbia.  In this study, patients with mild to moderate Alzheimer’s were given antibody preparations, immunoglobulin preparations, which were obtained by pooling plasma from numerous blood donors.  This sterile, medical product, IVIG, intravenous immunoglobulin, consists mostly of immunoglobulins, antibodies,  and is administered intravenously (IV). 

After receiving IVIG twice a month for three years, patient’s ‘ ability to function or think, their mood, or memory did not worsen over the three years. [Untreated Alzheimer’s disease patients typically show measurable declines in 3 to 6 months.]

The FDA, The U.S. Food and Drug Administration, has approved the use of IVIG for only six conditions.  However, it has been used “off-label”, to try and treat about 50 other conditions, including infectious diseases, a wide-range of autoimmune conditions, organ transplant and cancer patients, blood, and neurological conditions to mention a few.

When practitioners are asked how s/he thinks IVIG works, the response is typically, except for infectious diseases, “we are not sure”.

 IVIG Contains Immunoglobulins and Smaller Immune Factors
IVIG contains antibodies to organisms such as streptococcus, hepatitis, measles, polio, etc., that can specifically neutralize infectious agents.  Other immunoglobulins may be directed  against specific immunological factors. 

However, viewing reported results in chronically ill populations, I have always been of the opinion that IVIG also contains cytokines, or cytokine-like immune molecules, with potent immune system-modulating properties, which help the body return to immune homeostasis, immune balance. 

 I suggest that the reason that Alzheimer’s patients receiving IVIG saw a stabilization of their symptoms, is that IVIG limited inflammatory responses and thus slowed the progression of disease.

 Alzheimer’s and Inflammatory Cytokine Levels
This supposition is further supported by the fact that animal models suggest that excessive production of inflammatory cytokines, inflammatory messages, are implicated in Alzheimer’s disease. These animals have a condition similar to human Alzheimer’s, and also have higher levels of inflammatory cytokines in their blood.  When a drug was administered that inhibited the cytokines, there was less damage to nerve cells and neurological outcomes in the animals improved.  

 The scientists suggest that blocking production of high amounts of inflammatory cytokines may be beneficial for any number of brain conditions, such as “Alzheimer’s and Parkinson’s disease, multiple sclerosis (MS), motor neurone disease, frontotemporal dementia, and complications from traumatic brain injury.” (1)

 Immune Homeostasis, Immune Balance the Key to Health
Thus improvements, or at least delay in the onset of Alzheimer’s, or other brain –associated conditions, may be associated with the body achieving immune homeostasis.  A body in inflammatory balance controls the immune system’s  inappropriate inflammatory responses which otherwise may lead to damage of bystander tissues.

Feel free to contact Dr. Hellen at DrHellen@DrHellenGreenblatt.info with questions or to consult with her. A message may also be left at: 1.302-265.3870 or click on: http://drhellengreenblatt.info/contact-dr-hellen/.

 


www.medpagetoday.com/MeetingCoverage/AAIC/33780
http://emedicine.medscape.com/article/210367-overview#aw2aab6b3
www.alz.org/aaic/tues_1030amct_ivig_trial.asp
www.jneurosci.org/content/32/30/10201.abstract?sid=349221d1-e12f-411a-80a6-80285ed5db54
www.ncbi.nlm.nih.gov/pubmed/22806462

The journal of the American Geriatrics Society, just released a study of older women suggesting  that women, and we assume men as well, add years of healthy living by staying active and increasing their consumption of fruits and vegetables. 

 Women between the ages of 70 to 79 years were followed for a five-year period.  Investigators monitored the amount of physical activity they reported, and their carotenoid blood levels.  [Carotenoids are a class of pigmented, phyto [plant] nutrients found in the yellow, orange, and plants.  Blood levels of carotenoids are associated with the quantity of vegetables and fruits consumed.  The more fruit and veggies consumed, the higher the levels of carotenoids in the bloodstream.]

In the study, women that were most physically active and consumed large amounts of fruits and vegetables, were eight times more likely to be alive after the study’s five years of follow-up, compared to women who were not active, and did not eat many fruits and vegetables.

 Exercise increases survival times

More than half of the 713 participants (53%) did no exercise, 21% were moderately active, and the 26% were very active.  The active women engaged in twice the amount of activity as did women who were not active.  Active woman reported that they walked, or were involved in strength training, bowling, dancing, household, or outdoor chores.  Physical activity resulted in active woman experiencing five-year death rates 71% lower than those of the least active women.

 Fruits and vegetable consumption increases survival times

During the five-year follow-up period, women who consumed the most fruits and vegetables, and had the highest blood levels of carotenoids, were 46 percent less likely to die than woman that ate fewer fruits and vegetables.  Blood carotenoid levels were 12% higher in the women who survived, compared to blood samples taken from women that would die earlier.

 This study supports previous results demonstrating that eating more vegetables and fruits, and consuming moderate amounts of wine products, which also contain phytonutrients,  is linked to people living longer.

 Down-regulation of inflammation:  A probable reason for the reported results.

Most scientists have only vague ideas as to why exercise, and heightened consumption of fruits and vegetables should make a difference in longevity.  However, decades of literature reviews, and successful counseling of individuals in the importance of balancing immune system inflammation, make it evident to me, that exercise and healthy food consumption helps the body limit run-away inflammatory responses, and therefore helps the body balance its natural levels of inflammation.

 Inflammation is the body’s protective response to infection, cancer cell growth, and injury.  However, when inflammatory responses are not controlled, inflammation ends up doing more harm than good, and becomes the origin of most illnesses.

 It has been documented that unhealthy aging is accompanied by excessive inflammation with increases in cytokines that cause inflammation, and inflammatory markers such as C-reactive protein (CRP).

 But the body expends a great deal of energy to naturally control inflammatory responses, and return to immune homeostasis, immune balance.   So for example, moderate exercise lowers inflammation. 

Every time muscle contraction occurs, potent anti-inflammatory cytokines are released.  Therefore, as the women in this study were physically active, their bodies were naturally reducing the amount of inflammation in their bodies.

 As to the contribution of fruits and vegetables in lowering inflammation, hundreds of studies support the fact that carotenoids affect cytokines, the immune system messengers that modulate inflammation. 

 There are many ways to help the body modulate immune system-generated inflammatory responses, but simple lifestyle changes such as regular exercise, and increased consumption of fruits and vegetables, are two simple steps to consider for a healthier, longer, and more active life.

www.ncbi.nlm.nih.gov/pubmed/22587851

www.ncbi.nlm.nih.gov/pubmed/22162208

www.sciencedaily.com/releases/2012/05/120530100512.htm

www.sciencedaily.com/releases/2009/06/090624093353.htm

 www.ncbi.nlm.nih.gov/pubmed/19549997

www.ncbi.nlm.nih.gov/pubmed/22483785

www.ncbi.nlm.nih.gov/pubmed/22473333

www.ncbi.nlm.nih.gov/pubmed/22708923

The retina is the “flat screen” at the back of the eye onto which light is projected when we look at an object.  The center of the retina is called the macula.  When it is damaged, a condition called  macular degeneration, there is a “hole” at the center of one’s vision, making it difficult to recognize faces, read, or drive a car.

 As people grow older, they are at greater risk of getting macular degeneration.    Risk factors for this condition are:  being Caucasian, obese, female, and having a family history of macular degeneration.  High blood pressure, high cholesterol, and eating few fruits and vegetables, also add to one’s risk.

 However, the greatest known risk of damaging the retina comes from smoking tobacco.  Current and former smokers have 6.6 times the chance of developing macular degeneration as compared to those who never smoked. [Unfortunately, if you smoked one or more packs a day, even having quit 15 years previously, still increases the risk that you will have damaged your retina in some way.]

Even after decades of study, we do not understand the underlying mechanisms of macular degeneration. Increasingly however, the literature suggests that inflammation is a major contributor to destruction of the retina.

Immune system inflammation is the body’s first line of defense against pathogens such as viruses, bacteria, fungi, and parasites.  Inflammation is also important to control mutating, cancer cells. 

 However, excessive amounts of tissue-damaging inflammation can damage healthy neighboring tissue.  High sensitivity C-reactive protein (hs-CRP) is a blood marker associated with inflammation, and an indication that too great an inflammatory response is being generated by the immune system.

  A seven year study of hs-CRP levels of 4900 people was conducted in the Netherlands.  Individuals with high levels of C-reactive protein had a significantly greater risk of acquiring macular degeneration compared to those with “normal” baselines of the inflammatory marker. Additionally, other studies suggest that 75% of patients with macular degeneration have “inflammatory” genes that release pro-inflammatory cytokines that are associated with the condition.

 Some clinicians have recommmended using-steroidal anti-inflammatory medications to control macular degeneration, yet contradictory studies suggest that frequent aspirin use leads to macular degeneration. 

 We know that high aspirin consumption leads to excessive bleeding in digestive tracts and the eyes.  Perhaps the association of high aspirin use and macular degeneration is due the bleeding aspect of excessive aspirin consumption.

Inflammation is important for our survival, but it must be the appropriate amount of inflammation; it must be a balanced response of just enough inflammation to defend and heal, but not so much that it damages tissues.

Controlling excessive inflammation, without  the  side-effects of medications such as bleeding,  would likely help limit degeneration of the retina.

 www.blindness.org/index.php?option=com_content&view=article&id=46&Itemid=56

www.ophsource.org/periodicals/ophtha/article/S0161-6420(00)00580-7/abstract

www.ncbi.nlm.nih.gov/pubmed/21920607

www.ncbi.nlm.nih.gov/pubmed/21183941

www.ncbi.nlm.nih.gov/pubmed/17923549

www.csmd.ucsb.edu/news/md_science_article.pdf

As I have shared with readers and audiences over the years, when someone ages poorly, it results from decades of inflammatory imbalances.

Inflammation is necessary for the body to defend itself from pathogens and mutating cells, and for the body to heal itself after trauma or disease.

However, when the immune system produces excessive levels of inflammation, and does not correctly limit the amount of inflammation after its task has been completed, then inflammation becomes associated with unhealthy aging, and chronic disease.

For example, it is apparent that neurological diseases are affected, if not triggered by, inflammatory responses of the immune system.

 Immune cells of the brain and nervous system release inflammatory factors, cytokines and complex mixtures of other small immune molecules.

 These factors result in nervous cell and immune system inflammation and eventually, death of nerve cells.

 Last month, the journal of Immunity and Aging reported the results of genetic and immunological studies of Sicilian centenarians, individuals that are 100 years or older.

The researchers concluded that these individuals, all active and “in relatively good health”, survived longer than their cohorts, because their immune system was at “optimal performance” and that they were able to control inappropriate levels of inflammation.

 More evidence for the contribution of inflammation to aging poorly, for example cognitive abilities, is seen in a seemingly irrelevant study in which the use of fish oils was shown to counteract the negative effects of sugar drinks.

In this study, rats learned how to run a maze.  After their lesions, one group of rats was fed a sugary solution for over 6 weeks. After six months, the rats ran the maze again from memory.

Rats that were on the sugar, could not remember how to run the maze, but those on sugar along with  omega-3 fatty acids, were able to run it. The omega-3 fatty acids counteracted the negative effects of the sugary diet.

We know that high sugar consumption results in increasing size of fat cells, adipose tissue, and that fat cells release inflammatory molecules that are associated with the cardiovascular, joint, and insulin-related issues seen in obese individuals.

In addition, it has been shown that there are compounds in omega-3 fatty acids that counteract inflammatory responses.

Therefore, the results of the maze study may be attributable to the fact that the omega-3 helped down-regulate pro-inflammatory cytokines, messengers that initiate the inflammatory process.

During the past decades, I have watched the health outcomes of older individuals that have followed a regimen that maintains inflammatory balance.

In their 70s, 80s, and early 90s, they work full days, sometimes in physically-demanding positions, are on little or no medication, and find that they are more active, than individuals 20 years their junior.

Balanced immune inflammation, immune homeostasis, is the key to an active life.

One must generate enough inflammation to defend oneself from infectious disease, and help the body heal, but a healthy person has to be able to limit and control  inflammatory responses at appropriate levels for the tasks at hand.

www.immunityageing.com/content/9/1/8/abstract
www.ncbi.nlm.nih.gov/pubmed/22404117
www.ncbi.nlm.nih.gov/pubmed/16613757
www.ncbi.nlm.nih.gov/pubmed/22535513
archpsyc.jamanetwork.com/article.aspx?volume=66&issue=11&page=1263
www.ncbi.nlm.nih.gov/pubmed/22566778

Through the years, I have spoken with many individuals, usually, women, who have now been diagnosed with fibromyalgia.  Fibromyalgia is a condition in which individuals suffer from chronic pain, and have tenderness in about a dozen different spots in the body, and have “brain fog”.   They suffer from unremitting fatigue, bowel problems, difficulty in sleeping through the night, and waking up unrefreshed.  As would be expected, they are depressed and anxious as well.

 There are some physicians, even now, that think fibromyalgia “is all in the minds” of their patients.  Some studies have shown, that compared to the general population, individuals with fibromyalgia have significantly higher levels of depression and anxiety.  [Now why someone who is in pain and tired much of the time, would be depressed is beyond me.]

 I once spoke to a male physician who said that he always thought that fibromyalgia was “just” a psychological problem, having nothing to do with biology.  I asked him why he used the past tense, and he said to me, “because I got it!”. 

 Now that the pharmaceutical industry has come out with at least three FDA-approved medications for fibromyalgia, it evidently means that fibromyalgia can now be classified as a disease, and many clinicians treat it as such.  

Many patients have differing success when using these prescription medications.  The three pharmaceuticals reduced pain symptoms by only 30%.  Some of the medications made a difference in fatigue, but not in sleep patterns.  Many of these medications result in side effects ranging from insomnia (which they were trying to combat in the beginning!), nausea, and diarrhea.  Unfortunately for individuals suffering with fibromyalgia, many patients find that if the medication does work for them, too often it is for only a short-period of time, for as little as six months total.

Most clinicians state that the cause of fibromyalgia is unknown, but that “painful tissues” are not associated with inflammation. 

I respectfully suggest that inflammatory responses are major contributors to the pain and discomfort those individuals with fibromyalgia experience.  Indeed, I cannot imagine that a person can feel pain, in the absence of inflammation.

Increasingly, the literature suggests that fibromyalgia, and other neuromuscular conditions are characterized by low-grade inflammation.  Inflammatory cytokines such as tumor necrosis factor-alpha and IL-1, and other immunological factors, have been found to be at higher levels than “normals” and may be resulting in the fatigue and flu-like illness experienced by individuals with fibromyalgia.

Controlling run-away inflammation by returning to immune homeostasis, immune balance, has, in my experience, resulted in dramatic differences in the quality of life of individuals suffering with fibromyalgia.  These individuals have tried other approaches with only limited success, so why not support balanced immune responses?

Medscape Family Medicine 2012 WebMD, LLC
www.actabiomedica.it/data/2007/2_2007/fietta.pdf
www.medicinenet.com/fibromyalgia/article.htm
www.ncbi.nlm.nih.gov/pubmed/21975140
www.ncbi.nlm.nih.gov/pubmed/19957871

 

Obstructive sleep apnea syndrome  (OSAS) occurs when an individual repeatedly stops breathing, sometimes as many as 1-2 times a minute during their sleep.  It is most frequently associated with heavy snoring, broad swings in heart rate, and, as one would expect, extreme daytime sleepiness.  Those that suffer with sleep apnea are prone to accidents; they are twice as likely to be involved in car crashes as compared to individuals without the condition.

 The relationship between inflammation and sleep apnea is complicated, with not only inflammation of the airways, but  body-wide inflammation as well.

 As with other inflammatory conditions, obstructive sleep apnea is associated with cardiovascular disease, diabetes, and obesity.  Visceral fat, belly fat, is a major predictor of having obstructive sleep apnea syndrome, since fat cells produce large amounts of immune modulating molecules, that trigger inflammation.

 People suffering with sleep apnea have complex imbalances of immune factors, cytokines.  Their levels of immune modulating cytokines, such as tumor necrosis factor and interleukin (IL)-6, are markedly high, as are levels of other inflammatory proteins, including  C-reactive protein (hsCRP). [CRP is a blood protein typically associated with the presence and amount of inflammation in the body.]  Additionally,  hormones that regulate insulin and hunger levels are higher than levels found in those without sleep apnea.

 There is conflicting data about the affect of CPAPs, continuous positive airway pressure breathing devices,  on inflammation. Some studies suggest that the devices help lower the number of inflammatory molecules circulating in the body, other studies suggest that using a CPAP increases inflammation.

 Successfully battling disease, and healing , is determined by inflammatory immune cells and the types and ratios of cytokines they generate.  Restoring balance, immune homeostasis, to the body, helps the body stay healthy, and recover rapidly when in ill health.

emedicine.medscape.com/article/295807-overview
www.sciencedaily.com/releases/2008/02/080218214401.htm
www.ncbi.nlm.nih.gov/pubmed/22515302
www.chestjournal.chestpubs.org/content/127/3/1074.full
www.chestjournal.chestpubs.org/content/126/1/1.long
www.mayoclinic.com/health/sleep-apnea/DS00148
www.ncbi.nlm.nih.gov/pubmed/22408197

The concept of epigenetics was first introduced in the 1940s, and its implications on how we modulate inflammation through its processes are intriguing and exciting.

For most of my scientific career, we were taught that biological processes of the body were pre-determined by genes. It was said that DNA’s message was set-in-stone, and except through mutations which might result in cancer, or mutations and recombinations of genetic material that were handed down from one generation to another, the message encoded by DNA was unchanging.

Accumulating evidence suggests that altering our diet, life style, and environment, significantly influences gene expression; the way that the body translates the DNA message. We can change the affect our genes have on our physiological and emotional well-being.

It never ceases to amaze me that the medical profession writes off conditions such as arthritis, heart disease, cancer, strokes, Alzheimer’s etc. as being the result of “aging”; basically, saying to their patient, “you have to live with it because you are getting old”.

Instead, health practitioners might better focus on the fact that imbalances of inflammatory and anti-inflammatory responses contribute to health issues. Directing the emphasis on life style changes would enable individuals to take steps towards breaking the inflammation cycle, literally affecting the DNA message, and the resulting quality of their lives.

There are simple approaches that help maintain immune balance, immune homeostasis. Two such changes are: limiting the size of fat cells, and exercise. Fat cells, especially around our abdominal area, produce large amounts of pro-inflammatory cytokines, that trigger inappropriate levels of inflammation.

Exercise is a way to neutralize these molecules since contracting our muscles releases potent anti-inflammatory cytokines.

Additionally, the daily consumption of two or more servings of hyperimmune egg can go a long way toward supporting the body’s natural immune-rebalancing attempts.

In the controversy of genes vs. nurture, we now know that it is a combination of both that makes the difference. We can help regulate what our genes “say” by how we choose to live our lives.

www.sciencemag.org/site/feature/plus/sfg/resources/res_epigenetics.xhtml

www.ncbi.nlm.nih.gov/pubmed/22004920.1

target=”_blank”>articles.mercola.com/sites/articles/archive/2012/04/11/epigenetic-vs-determinism.aspx

www.ncbi.nlm.nih.gov/pubmed/22428854

www.ncbi.nlm.nih.gov/pubmed/20388091

 

(Please see prior posting)

ACHIEVING INFLAMMATORY HOMEOSTASIS, IMMUNE BALANCE, NATURALLY

CONTROL INFLAMMATION

Restoring immune inflammatory balance, homeostasis, may reduce diabetic symptoms, help guard against infections, and contribute to overall health by letting the body heal itself. Lifestyle changes, rather than medication, are the best ways to regain immune balance, inflammatory homeostasis.

BECOME PHYSICALLY ACTIVE.

Muscles release anti-inflammatory molecules every time they contract. To help balance the levels of inflammation in the body, try to be physically active at least 150 minutes a week. Walk to the bus at a brisk pace. Stand, instead of sitting. Work faster when in the garden. Exercise while watching TV. Just get moving!

This week’s pre-publication article from the journal, Diabetes Care, reports that diabetics that participated in aerobic and resistance training twice a week were more fit than controls, even when they personally did not have any weight loss. Moreover, another publication this week in the journal, Endocrine, reports that even without weight reductions, exercise by itself helps control blood sugar levels.

GET TO YOUR IDEAL WEIGHT.

Obese individuals are at greater risk of getting diabetes. Fat cells release pro-inflammatory cytokines, messages that result in inflammation. Many diabetic symptoms are reduced, even with minimal weight loss.

Make smarter beverage and food choices. The most recent discussions about foods is to ignore the amount of fat you take in, and instead, concentrate on decreasing your total carbohydrate intake.

 Limit your intake of:

  • Liquid carbohydrates such as sodas, either regular or “diet”, fruit juices, “energy” drinks, beer.
  • Fried foods.
  • Starches, such as corn, white rice, chips, nachos, French fries.
  • White flour such as found in breads, pasta, cakes, desserts.

 Fill half your plate with vegetables and colorful fruit. The following foods are reportedly helpful to diabetics: Brewer’s yeast, broccoli, buckwheat, liver, okra, peas, and spinach.

VITAMIN D MAY PLAY A ROLE IN BALANCING INFLAMMATORY RESPONSES. Recent studies suggest that vitamin D, actually a hormone-like biochemical, is involved in cell growth and immunity. Studies suggest that vitamin D suppresses proinflammatory cytokines and increases anti-inflammatory cytokines. Organ systems such as liver, skin, thymus, small intestines, and pancreas have cells that bind a form of vitamin D. Certain groups of diabetics have low levels of vitamin D.

The body produces its own vitamin D when sun exposure is appropriate. Moderate sun exposure during the summer months, stimulates the production of its vitamin D. In temperate climes, supplementation may be prudent.

 OMEGA-3 FATTY ACIDS. There are suggestions in the scientific literature that diabetics may benefit from consuming omega-3 fish oils. Consume 2-3 servings of fish/week or take supplements.

MODERATE COFFEE CONSUMPTION. Certain compounds in coffee may help decrease inflammation. Moderate consumption of coffee may be helpful to diabetics.

HYPERIMMUNE EGG. Immunologists have shown that consumption of multiple servings/day of hyperimmune egg is a natural way to help the body regain its immune homeostasis.

IN SUMMARY

Important steps that a diabetic can take are to become physically active, control their diet and weight, and are other steps to reduce inappropriate inflammation.


www.ncbi.nlm.nih.gov/pubmed/22399699

www.ncbi.nlm.nih.gov/pubmed/22407494

www.ncbi.nlm.nih.gov/pubmed/20181814

www.ncbi.nlm.nih.gov/pubmed/22404117

www.ncbi.nlm.nih.gov/pubmed/22397028

www.ncbi.nlm.nih.gov/pubmed/19957870

www.ncbi.nlm.nih.gov/pubmed/21593500

www.ncbi.nlm.nih.gov/pubmed/22375372

 

 

Many patients that undergo chemotherapy report lingering effects of the disease, or from treatment protocols. Some individuals report that experience problems with cognition, clear thinking, memory, focus, concentration, and staying organized which they call “brain fog” or “chemo brain.”

The relationship between inflammation and cancer is still under intense study. Immune inflammation plays a major role during different stages of tumor development, from recognition of the cancer cells, to metastasis, to resolution of the disease. There are proven complex interactions between immune and cancer cells during which there appears to be “cross-talk.”

Chemotherapeutic medications are, of necessity, cytotoxic. The medications cause the death of cells (apoptosis) by programming their death or by interfering with certain biochemical processes within the cell.

The relationship of inflammatory immune cells and dead cells is a complex one. Whenever a cell dies because of infection or injury, inflammatory immune cells release inflammatory cytokines, messages that activate immune cells to clean up debris, and start the healing process.

Chemotherapy, in which both healthy and cancerous cells are killed, can have unintended effects. The medications can damage immune cells and their DNA; the very cells that the body needs to stop cancer cells from multiplying, to clean up the dead cells, and heal the body after cytotoxic challenge.

An example of such a possible problem is tumor lysis syndrome. When large numbers of cells are killed by chemotherapeutic agents, the dying cells release vast amounts of inflammatory-triggering compounds. The body is simply overwhelmed by these factors, resulting in significant immunological and chemical disruptions throughout the body.

A limited number of studies, still to be replicated, suggest that long after treatment has ended, healthy brain cells continue to die off. And at least one study has shown altered brain structure in individuals that had undergone chemotherapy a year previously. These results however, were not seen in patients that had received chemotherapy three years previously.

The relationship between inflammation, cancer, and cancer therapy, is not understood. However, the available science suggests that limiting excessive inflammatory responses by the immune system, may help minimize the adverse effects of chemotherapy, especially as it relates to the brain.

 

http://www.mayoclinic.com/health/chemo-brain/DS01109


www.ncbi.nlm.nih.gov/pubmed/20303878


www.ncbi.nlm.nih.gov/pubmed/21545608

www.nature.com/cdd/journal/v15/n1/full/4402255a.html

www.ncbi.nlm.nih.gov/pubmed/22294874

www.nature.com/nrclinonc/journal/v3/n8/full/ncponc0581.html

jbiol.com/content/7/4/11

 

For years, physicians told their (overwhelmingly female) patients, that patient complaints of skeletal and muscle pains, sleep disorders, overwhelming fatigue not improved by bed rest, brain “fog”, and lack of stamina, were “all in their mind”.

However once pharmaceutical medications were introduced into the market place to help decrease some of these symptoms, health practitioners started diagnosing these conditions as chronic fatigue syndrome, CFS or ME, myalgic encephalomyelitis.

Viral Involvement Controversial

In 2009, an article in the prestigious journal Science reported that 95% of subjects with chronic fatigue syndrome were infected with a specific virus and/or had antibodies to that virus. The investigational team emphasized that these findings did not prove that there was a link between this virus and chronic fatigue, but that the virus might be “a contributing factor”.

Late this past year, the editors of Science retracted the controversial article due to the poor quality controls, and omissions in the description of certain figures. Additionally, other laboratories have been unable to replicate the results.

This specific virus may not have been responsible for ME, but the concept is sound since other studies have suggested that bacterial and viral infections can trigger inflammatory immune diseases such as heart valve damage, arthritis, multiple sclerosis, diabetes, and systemic lupus erythematosus (SLE).

Autoimmune Inflammatory Conditions

Inflammatory diseases are often manifestations of an autoimmune inflammatory response. Autoimmune disease occurs when the immune system “over-reacts” to a stimulus and attacks its own cells with excessive inflammatory responses.

Digestive Tract-A Large Immune Organ

The lining of the digestive tract is heavily populated by immune cells and is considered a major immune organ. Many CFS patients complain of gut dysfunction, and have been diagnosed with irritable bowel syndrome (IBS) and with proinflammatory cytokine production.

Increase in Inflammatory Markers

Immunologically, individuals with chronic fatigue have increased blood levels of inflammatory compounds, such as C-reactive protein (CRP), and exhibit immunological abnormalities, including increased numbers of activated immune cells, and high levels of inflammatory cytokines, indicative of inflammation.

“… [T]he simplest way to think about … findings [such as these-HCG] is that people with increased inflammation–from whatever source–are more likely than others to develop a range of symptoms that frequently lead to a diagnosis of a condition such as CFS …” says William C. Reeves, MD, Chief of the Chronic Viral Diseases Branch, the Centers for Disease Control and Prevention (CDC). “

Role of Immune Inflammation

Immune inflammation helps defend the body from infection and heals the body after injury. However, when immune inflammation is in “overdrive”, autoimmune and other autoinflammatory conditions result.

Making certain lifestyle changes will contribute to lowering the amount of inflammation in the body. These are: a) becoming physically active so that muscle contractions generate naturally-occuring anti-inflammatory molecules and b) controlling one’s weight to reduce the levels of inflammatory compounds being released by fat cells.

Other steps to consider are moderate exposure to sunlight (or taking vitamin D3 supplements), consuming omega-3, and adding hyperimmune egg to one’s diet.

Immune Balance

Good health is determined by the balance between the pro-inflammatory and anti-inflammatory cytokines produced by our immune cells; maintaining these immune factors in their appropriate amounts, is essential.

www.sciencemag.org/content/326/5952/585
www.sciencemag.org/content/334/6063/1636.1
www.sciencedirect.com/science/article/pii/S0889159108004261
www.nutritionandmetabolism.com/content/7/1/79
www.ncbi.nlm.nih.gov/pubmed/19758205
cmr.asm.org/content/9/4/532.abstract
www.ncbi.nlm.nih.gov/pubmed/16380690
www.ncbi.nlm.nih.gov/pubmed/18801465

Alcohol hangovers occur when blood alcohol concentrations (BAC) return to zero. The event is characterized by pounding headache, sensitivity to lights and loud noises, dizziness, drowsiness, nausea, vomiting, dry mouth, sweating, concentration problems, hyper-excitability, and anxiety and/or depression.

The biology of hangovers is complex and surprisingly, has not been well-researched. Dehydration and sleep deprivation may be contributors to the state of being hung over, but biological changes during suggest that, as with a majority of disease, imbalances of immune factors, especially excessive production of inflammatory cytokines, may be the culprit.

Hangovers are reminiscent of “sickness behavior”, the feelings that sick individuals have during the course of fighting an infection. “Feeling poorly” is the effect of increased levels of proinflammatory cytokines, that increase inflammation in the brain.

During inflammation, a great deal of cross-talk, mediated by cytokines, goes on between the immune system, the brain, and the intestines, which stimulates a wide range of physical, hormonal, nervous , gastrointestinal, and emotional responses.

Increased levels of inflammatory cytokines, such as IL-12 and interferon-gamma (IFN-gamma) are found in individuals suffering from hangovers. Additionally IL-10 , which suppresses inflammatory cytokines, is also found at higher levels in hangover subjects.

C-reactive proteins (CRP) are found in the blood and are considered an excellent marker for inflammation in the body. High levels of C-reactive protein are strongly associated with the severity of hangover events. The response may be related to inflammation induced by excessive ingestion of certain alcohol components such as congeners, or alcohol metabolites.

Numerous anecdotal reports suggest that when the body is in immune inflammatory balance, that hangovers will not occur at all, or, will be severely limited in their scope.


http://alcalc.oxfordjournals.org/content/43/2/124.full
http://www.ncbi.nlm.nih.gov/pubmed/15226168
http://www.ncbi.nlm.nih.gov/pubmed/14693266
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC508465/pdf/1002641.pdf
http://www.ncbi.nlm.nih.gov/pubmed/20712594
http://www.ncbi.nlm.nih.gov/pubmed/11259077

Exercise is essential for workers such as firefighters and paramedics that have physically-and emotionally-demanding jobs, and is mandated by most departments.

According to a study by the University of Arizona, Tucson, AZ and the Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, 30% of the strains and sprains that firefighters and paramedics experienced, happened as they were working out. Seventeen percent of injuries, and almost half of time off work for injuries, were caused by strains and sprains resulting from workers carrying individuals.

Pain and inflammation “feed one another”. Pain triggers more inflammation and inflammation  leads to more pain. It is not clear how the body senses pain, nor biochemically, the exact events that lead to the sensation of pain. We know however, that pain signals from our back or limbs travel along nerve cells to the spinal cord and up to the brain, and that inflammation in the spinal cord and brain is either the direct cause of pain, or a major contributor to pain sensations that we experience.

When muscles and tissues are injured, immune cells respond by entering the area and releasing cellular factors (e.g., cytokines) that will up-regulate inflammation as a way to help the body heal.

However, it is as important for the body to decrease its inflammatory responses after a challenge is met, as it is to increase the response in the first place. Decreases in inflammatory responses, down-regulation, result from the production of different amounts of anti-inflammatory cytokines and their ratio to pro-inflammatory cytokines that cause inflammation. It all about the appropriate balance of immune responses, immune homeostasis.

(Please watch for the next posting discussing natural methods of helping the body achieve immune homeostasis, and recover, and heal faster.)

injuryprevention.bmj.com/content/early/2011/11/03/injuryprev-2011
www.nature.com/nrneurol/journal/v7/n3/full/nrneurol.2011.4.html
www.ncbi.nlm.nih.gov/pubmed/19096368
www.ncbi.nlm.nih.gov/pubmed/22119349
www.gluegrant.org/inflammation101.htm
http://www.ncbi.nlm.nih.gov/pubmed?term=Curr%20Drug%20Targets%20Immune%20Endocr%20Metabol%20Disord%202005%205%3A413

A recent guest post on kevinmd.com by Sophie Lee expressed her frustration and anger at physicians who dismiss her reports of pain with her severe bouts of irritable bowel syndrome (IBS). She repeatedly hears, “it isn’t really serious” “you will just have to live with it, etc.  [ www.ibstales.com ].

I just do not get why conventional “wisdom” is that IBS is not an inflammatory disorder. Perhaps pain is possible without inflammation, but that would be atypical. My contention is that if the immune system was in homeostasis, autoimmune disease would either not occur, or it would be limited.

For years I have been questioning “experts”, how is it that IBS is categorized as an autoimmune* disease, yet you claim there is no inflammatory response in the gut?

Current research supports my contention. Recent studies are providing evidence that low levels of inflammation, along with immune mast and other immune cells, are found in the small and large intestines. Mast cells are typically associated with allergic reactions such as runny noses, watery eyes, swelling, and excessive mucous. The mast cells in the intestines appear to be involved in immune homeostasis, in helping the immune system balance.

Interestingly, many of the immune cells found in the gut are in close proximity to nerve cells. .. “Cross-talk” between these cells may explain the pain and other symptoms that individuals experience, and support the hypothesis of a brain-gut axis event in IBS.

It is time for individuals that have “tried everything”, to give their bodies a chance to heal naturally. The immune system has caused the problem, and the immune system can be gently guided to down-regulate overly active responses.

The key to greater comfort may be as simple as helping the body return to immune homeostasis. I hold a patent in the area of immune homeostasis and gut health, and numerous anecdotal reports suggest that balancing immune inflammatory responses makes a major difference in the quality of life of such individuals. Additionally there is a published clinical report by Mark Morningstar, DC, Grand Blanc, MI supporting the relationship between immune homeostasis and healthy bowel function.

One has everything to gain by letting one’s own body rebalance and limit inflammatory responses.

*The immune system mistakenly attacks “self”, the body’s own healthy tissues.

ncbi.nlm.nih.gov/pubmed/22053295
sciencedaily.com/releases/2010/06/100607111308.htm
ncbi.nlm.nih.gov/pubmed/18627650
ncbi.nlm.nih.gov/pubmed/19674619
patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6,803,035.PN.&OS=PN/6,803,035&RS=PN/6,803,035

A properly functioning immune system protects the body against infections by bacteria, viruses, fungi and other pathogens, and helps it heal. When our bodies detect a threat, or a stimulus that is “perceived” to be a threat, it orchestrates a delicate but highly aggressive immune inflammatory response to meet that threat.

There are two initial phases of immune responses:

  • Innate/early phase — a “built-in” or “automatic” response that is prepared at all times to defend the body against infection and cell mutations, such as those seen in cancers, and
  • Acquired– a more “educated” immune response that takes time to evolve in response to a specific trigger.

Inflammation is a complex event during which immune cells migrate into an area in response to various immune factors. These messages, such as cytokines, are used to to communicate and coordinate an organize attack against pathogens, or to help the healing process. After the threat has been resolved, other immune cells come in to carry away dead organisms and cells, and start the repair process.

A well-balanced immune system, a system in immune homeostasis, will mount enough of an inflammatory response to eliminate the threat, and then go on to repair damaged tissues. However, problems may arise if the immune system continues to generate an inflammatory responses after a challenge has been met —when inflammatory responses do not lower in intensity.

In such cases, the immune system is “over-responsive”; it is unbalanced, out of homeostasis. An over-active immune system leads to conditions where the body starts to destroy its own healthy tissue (e.g. diabetes, thyroid, lupus, multiple sclerosis, fibromyalgia, etc.) or it may lead to allergies and chemical sensitivities, or poor healing.

Many people have the mistaken impression that “boosting” immune function at all times is useful. This is simplistic. People with autoimmune conditions, such as those mentioned above, are already “over responding”. The last thing they need is to further “boost” their immune response, increase their autoimmune responsiveness.

Another example of “boosting” immune response is artificially increasing the level of natural killer (NK) cells within the body. NK cells often make up part of the body’s “early response”. “Boosting” numbers of certain white cells is unnatural and may cause other difficulties due to excessive numbers of these cells.

Increased levels of NK cells, as well as autoimmunity, have been associated with women who have difficulty conceiving. Women who have experienced spontaneous abortions and miscarriages, have higher than normal levels of NK cells.

Additionally, other types of specific immune cells, for example those that play a role in protecting the body from infection, may promote miscarriage and premature births, when they are at higher than normal levels.

The lesson here is that all of our immune cells and their components have to be balanced, or in a state of homeostasis, for our body to naturally heal and protect itself.

There are a number of simple steps that one can take to return the body to homeostasis, including using recovery proteins, exercise, smarter food choices, and maintenance of healthier weights.

http://www.ncbi.nlm.nih.gov/pubmed/20237962
http://www.ncbi.nlm.nih.gov/pubmed/20528832
http://www.ncbi.nlm.nih.gov/pubmed/21162648
 

css.php