Sunday, June 23, 2013

No Substitute for Liver, It will give you more stamina than the energizer bunny

So what makes liver so wonderful? Quite simply, it contains more nutrients, gram for gram, than any other food. In summary, liver provides:
  • An excellent source of high-quality protein
  • Nature’s most concentrated source of vitamin A
  • All the B vitamins in abundance, particularly vitamin B12
  • One of our best sources of folic acid
  • A highly usable form of iron
  • Trace elements such as copper, zinc and chromium; liver is our best source of copper
  • An unidentified anti-fatigue factor
  • CoQ10, a nutrient that is especially important for cardio-vascular function
  • A good source of purines, nitrogen-containing compounds that serve as precursors for DNA and RNA.

ANTI-FATIGUE FACTOR

Liver’s as-yet-unidentified anti-fatigue factor makes it a favorite with athletes and bodybuilders. The factor was described by Benjamin K. Ershoff, PhD, in a July 1951 article published in the Proceedings for the Society for Experimental Biology and Medicine.
Ershoff divided laboratory rats into three groups. The first ate a basic diet, fortified with 11 vitamins. The second ate the same diet, along with an additional supply of vitamin B complex. The third ate the original diet, but instead of vitamin B complex received 10 percent of rations as powdered liver.
A 1975 article published in Prevention magazine described the experiment as follows: "After several weeks, the animals were placed one by one into a drum of cold water from which they could not climb out. They literally were forced to sink or swim. Rats in the first group swam for an average 13.3 minutes before giving up. The second group, which had the added fortifications of B vitamins, swam for an average of 13.4 minutes. Of the last group of rats, the ones receiving liver, three swam for 63, 83 and 87 minutes. The other nine rats in this group were still swimming vigorously at the end of two hours when the test was terminated. Something in the liver had prevented them from becoming exhausted. To this day scientists have not been able to pin a label on this anti-fatigue factor."

Tuesday, June 18, 2013

Get Switched ON! Down your Eggs like Rocky and Speed up your brain by boosting ACH acetyl choline

During the course of the normal aging process, concentrations of ACh tend to decrease, resulting in the sporadic lapses of short-term memory that many elderly individuals tend to experience erupting to Alzheimer's if not checked.

Significant loss of cholinergic neurons is one of  the most significant biological explanation for this devastating Alzheimeir's condition.  Some of Ach functions include: the conduction of pain, the regulation of neuroendocrine function, the regulation of REM sleep cycles, and the process of learning and memory formation.  These neurons send major projections to the hippocampus, a structure particularly important for the normal formation of declarative memories.

Scientists have discovered that choline is necessary to produce phosphatidylcholine (PC).  Phosphatidylcholine is  crucial to synthesize a low density lipoprotein (VLDL) particle, which we need    to export fats from our livers.  Methionine acts as a precursor to choline and can  convert to phosphatidylethanolamine, which finally ends ups as phosphatidylcholine.


Thus, the combined deficiency of choline and methionine will severely impair our livers ability to release fats into the bloodstream.
Animal and plant foodsCholine (mg)
32 gram sunflower lecithin syrup544

15 gram soy lecithin granules450
5 ounces (142 g) raw beef liver473 
Large hardboiled egg113 
1 Whole raw egg,has over an average of 100mg of choline!
 Most experts believe you should eat the whole egg raw, which is also one the highest quality protein sources on the planet. 

Only diseased chickens lay salmonella-contaminated eggs. If you are obtaining high quality, cage-free, organic eggs , the risk virtually disappears. *****

Acetyl-N-Carnitine is a kind of amino acid that is able to increase the production of acetylcholine by donating a small molecule called acetyl (which is made up of two carbons atoms, three hydrogen ones, and an oxygen atom) to another compound, which is known as choline. Once choline receives this acetyl molecule, it becomes acetylcholine (hence the name). Taurine, another amino acid, has been shown to increase the levels of acetylcholine in the hippocampus, which is a part of the brain. 

Dehydroepiandrosterone (DHEA) and 

pregnenolone thrusts the release

 of acetylcholine in the hippocampus.  


This include dimethylaminoethanol (DMAE) which is a drug that slows the breakdown of choline in tissues outside of the brain. As a result, more choline is available to be turned into acetylcholine.

By adding a methyl group (CH3) to DMAE, choline (also called trimethylaminoethanol) is formed. The choline thus formed may then be used to make other valuable biochemicals, such as the major neurotransmitter acetylcholine.

Another drug, pyroglutamate, is also able to increase acetylcholine production by enhancing the production of other chemicals that cause more acetylcholine to be made.
Certain B vitamins are critical for the synthesis of acetylcholine, and a deficiency in them can cause decreased acetylcholine production. These include vitamin B1, B5, and B12.


Ginkgo biloba, stimulates the brain's adsorption of acetylcholine, and the lipid phosphatidylserine,  aids in the production and release of acetylcholine into the brain and reduces cortisol secretion.

GPC Choline (L-alpha-glycerylphosphorylcholine) is one of the best forms of choline to take as it is easily absorbed by the body.

Acetylcholine is important for memory and learning and is a neurotransmitter used throughout the body.  It controls muscle contraction for example.  Acetylcholine may be extremely important for long term memory and   It determines your brain speed.

  In contrast Anticholinergics generally have antisialagogue effects (decreasing saliva production), and most produce some level of sedation.

If you have too little, your brain is going to slow down.  The most extreme case of this is Alzheimer’s.   You can think of acetylcholine as a lubricant for your brain and body.  Acetylcholine along with dopamine are the neurotransmitters that turn your brain on.  They allow it to work hard and fast.  A lack of either one can lead to memory and attention problems.

Modafinil, Armodafinil, and Adrafinil are H3  (histamine receptor 3 antagonists) H3 antagonists also shove up concentrations of  extracellular acetylcholine , brain histamine,  noradrenaline,  & dopamine that are known to modulate cognitive processes. The ability to release brain histamine supports the effect on attention and vigilance, but histamine also modulates other cognitive domains such as short-term and long-term memory.   

Modafinil elevates hypothalamic histamine levels,[6] leading some researchers to consider modafinil a "wakefulness promoting agent" rather than a classic amphetamine-like stimulant.[7] Modafinil seems to inhibit the actions of the dopamine transporter, thus leading to an increase in extracellular and thus synaptic concentrations of dopamine


Histamine release in the brain triggers secondary release of excitatory neurotransmitters such as glutamate and acetylcholine via stimulation of H1receptors in the cerebral cortex. Consequently unlike the H1 antagonist antihistamines which are sedating, H3 antagonists have stimulant and nootropic effects, and are being researched as potential drugs for the treatment of neurodegenerative conditions such as Alzheimer's disease.

Galanthamine extract is a specific, competitive and reversible acetylcholinesterase
inhibitor. It is used in the manufacture of 
medications, such as Nivalin and Reminyl, both of which have been approved by the FDA. They are a strong (reversible) cholinesterase inhibitor, increasing the susceptibility of organisms to acetylcholine, and treat for mild to moderate dementia of Alzheimer's type in clinic.

Huperzine A is also an acetylcholinesterase inhibitorDamage to the cholinergic (acetylcholine-producing) system causes memory deficits associated with Alzheimer's disease. ACh has also been shown to promote REM sleep.  


Taking 200 milligrams of huperzine-A 30 minutes before bed can increase total REM by 20-30%. Huperzine-A, an extract of Huperzia serrata, slows the breakdown of the neurotransmitter acetylcholine. It is popular nootropic (smart drug), and I have used it in the past to accelerate learning and increase the incidence of lucid dreaming. I now only use huperzine-A for the first few weeks of language acquisition, and no more than three days per week to avoid side effects. Ironically, one documented side effect of overuse is insomnia. The brain is a sensitive instrument, and while generally well tolerated, this drug is contraindictated with some classes of medications. Speak with your doctor before using.


Neuro- transmitter:ACh
Acetylcholine

















Effects:↓Heart rate ↑Secretions (sweat, saliva) ↑Memory ↑Muscle contractions

Under healthy conditions REM sleep ‘turns-on' when activity levels of the biogenic amines (e.g. noradrenaline) decrease and activity levels ofacetylcholine increase. It is therefore not surprising to find that drugs that increase cholinergic activity generally tend to increase REM sleep and dream recall.

 Magnolia bark extract  contains eudesmol, an essential oil with possible antioxidant advantages.  Honokiol and magnolol (found in magnolia bark) can exert an increase in acetylcholine.


Deprenyl (selegiline) pre-treatment has been shown to protect cholinergic neurons from toxicity.



*****Only 0.003% percent of eggs are infected. The translation is that only one in every 30,000 eggs is contaminated with salmonella. This gives you an idea of how uncommon this problem actually is, so don't live in fear....down the hatch with those raw eggs, just like Rocky Balboa.

 You may feel sick and have loose stools, but this infection is easily treated by using high-quality probiotics that have plenty of good bacteria.  The majority of the people who contract salmonella aggressively using probiotics as treatment,just suffer with symptoms for a few hours.


Possible signs and symptoms of salmonella: include:Nausea, Vomiting, Abdominal pain, Diarrhea, Fever,, Chills Headache, Muscle pains and blood in the stool.  Signs and symptoms of salmonella infection generally last four to seven days, although it may take several months for your bowels to return to normal.

Saturday, June 15, 2013

Rapid recovery from major depression using magnesium treatment.

 Magnesium deficiency is occurring at epidemic rates, 80% is one estimate.   Magnesium  rbc (red blood cell testing) is the most accurate test,  serum magnesium tests are worthless.

Mega Dose magnesium sulfate increases testosterone levels in animal studies.

From a nutritional perspective, several research studies have shown certain minerals to be an effective natural insomnia remedy to help people fall asleep and stay asleep throughout the night. James F. Balch, M.D., author of Prescription for Nutritional Healing, writes: "A lack of the nutrients calcium and magnesium will cause you to wake up after a few hours and not be able to return to sleep."
Calcium is directly related to our cycles of sleep. In one study, published in the European Neurology Journal, researchers found that calcium levels in the body are higher during some of the deepest levels of sleep, such as the rapid eye movement (REM) phase. The study concluded that disturbances in sleep, especially the absence of REM deep sleep or disturbed REM sleep, are related to a calcium deficiency. Restoration to the normal course of sleep was achieved following the normalization of the blood calcium level.
William Sears, M.D. writes: "Calcium helps the brain use the amino acid tryptophan to manufacture the sleep-inducing substance melatonin. This explains why dairy products, which contain both tryptophan and calcium, are one of the top sleep-inducing foods."

Magnesium sulfate supplementation increases testosterone levels , and a magnesium-rich (brown rice) diet helps the elderly maintain testosterone levels.

There's been quite a bit of HYPE pimping MAGNESIUM L-THREONATE as a superior form of MAGNESIUM with claims of unique NOOTROPIC effects.

I've looked into what research exists to support these facts and I am sorry to report that the evidence simply does not stack up.

In short, there is conclusive substantiated scientific evidence that MAGNESIUM L-THREONATE does not in fact offer any superiority over MAGNESIUM SULFATE

The hype regarding MAGNESIUM L-THREONATE stems from claims that MAGNESIUM L-THREONATE increases BRAIN MAGNESIUM LEVELS to a greater extent than other magnesium forms, which would include MAGNESIUM SULFATE.

THIS IS A FALLACY

As is happens, administration of both MAGNESIUM SULFATE and MAGNESIUM L-THREONATE increase CEREBROSPINAL FLUID (CSF) LEVELS (= BRAIN LEVELS) of MAGNESIUM by exactly the same amount, namely 7-15%

The following study demonstrates that administration of MAGNESIUM SULFATE increases CEREBROSPINAL FLUID (CSF) LEVELS (= BRAIN LEVELS) of MAGNESIUM "by 15% and 11% relative to baseline":

Crit Care Med. 2005 Mar;33(3):661-6.

Analysis of the brain bioavailability of peripherally administered magnesium sulfate: A study in humans with acute brain injury undergoing prolonged induced hypermagnesemia.

McKee JA, Brewer RP, Macy GE, Phillips-Bute B, Campbell KA, Borel CO, Reynolds JD, Warner DS.

Source
Neurosciences Intensive Care Unit, Duke University Medical Center, Durham, NC, USA.


In magnesium deficiency, chronic insomnia is one of the main, central symptoms. Sleep is usually agitated with frequent nighttime awakenings. On the other hand, a high magnesium, low aluminum diet has been found to be associated with deeper, less interrupted sleep. This was proven in a study done by James Penland at the Human Nutrition Research Center in North Dakota. The study was titled "Effects of trace element nutrition on sleep patterns in adult women." It's important to note that a balanced ratio of calcium and magnesium is important to overall health, and these two minerals should be taken together for best results.



magnesium deficiency CAN cause insomnia.
A study conducted at the Human Nutrition Research Center in North Dakota, "Effects of Trace Element Nutrition on Sleep Patterns in Adult Women," proved conclusively that a diet high in magnesium and low in aluminum led to sounder, longer sleep.Researchers at the East Texas Medical Center and the University of North Carolina have discovered that vitamin D helps to regulate the sleep-wake cycle.  They've found a definite link between vitamin D deficiency and the current global epidemic of sleep disorders. 




There is a wealth of evidence that Magnesium Orotate is beneficial in situations ranging from athletic performance to survival of heart disease patients.  

Restoration to the normal course of sleep was achieved following the normalization of the blood calcium level.  As a note, calcium works best when its balanced with magnesium in a two to one ratio (with twice as much calcium as magnesium).




What are the causes of hypomagnesemia?

David R. Mouw, MD, PhD; Robyn A. Latessa, MD
University of North Carolina, MAHEC Family Practice Residency,  Asheville, NC
Elaine J. Sullo, MLS
East Carolina University, Laupus Library,  Greenville, NC

  EVIDENCE-BASED ANSWER

The causes of magnesium depletion and hypomagnesemia are decreased gastrointestinal (GI) absorption and increased renal loss. Decreased GI absorption is frequently due to diarrhea, malabsorption, and inadequate dietary intake. Common causes of excessive urinary loss are diuresis due to alcohol, glycosuria, and loop diuretics.
Medical conditions putting persons at high risk for hypomagnesemia are alcoholism, congestive heart failure, diabetes, chronic diarrhea, hypokalemia, hypocalcemia, and malnutrition

Sixty percent of cases of clinical depression are considered to be treatment-resistant depression (TRD). Magnesium-deficiency causes N-methyl-d-aspartate (NMDA) coupled calcium channels to be biased towards opening, causing neuronal injury and neurological dysfunction, which may appear to humans as major depression. Oral administration of magnesium to animals led to anti-depressant-like effects that were comparable to those of strong anti-depressant drugs. Cerebral spinal fluid (CSF)magnesium has been found low in treatment-resistant suicidal depression and in patients that have attempted suicide. Brain magnesium has been found low in TRD using phosphorous nuclear magnetic resonance spectroscopy, an accurate means for measuring brain magnesiumhttp://www.sciencedirect.com/science/article/pii/S0306987709007300


Magnesium Deficiency
Insomnia is one of the central, or neurotic, symptoms of chronic magnesium deficiency.  A number of parasomnias (night terrors; nocturnal verbal and motor automatisms; restless legs syndrome) may be related to magnesium deficiency.  Sleep in magnesium deficiency is usually agitated with frequent nocturnal awakenings. Nocturnal instrument monitoring reveals major disorders of sleep organization. The deficiency may be severe enough to be diagnosed on the basis of clearly low blood magnesium levels. Conversely, a high magnesium, low aluminum diet has been found to be associated with high-quality sleep time and few nighttime awakenings, and magnesiumsupplementation has been reported to reduce sleep latency and result in uninterrupted sleep. 



Case histories are presented showing rapid recovery (less than 7 days) from major depression using 125-300 mg of magnesium (as glycinate and taurinate) with each meal and at bedtime. Magnesium was found usually effective for treatment of depression in general use. Related and accompanying mental illnesses in these case histories including traumatic brain injury, headache, suicidal ideation, anxiety, irritability, insomnia, postpartum depression, cocaine, alcohol and tobacco abuse, hypersensitivity to calcium, short-term memory loss and IQ loss were also benefited. Dietary deficiencies of magnesium, coupled with excess calcium and stress may cause many cases of other related symptoms including agitation, anxiety, irritability, confusion, asthenia, sleeplessness, headache, delirium, hallucinations and hyperexcitability, with each of these having been previously documented. The possibility that magnesiumdeficiency is the cause of most major depression and related mental health problems including IQ loss and addiction is enormously important to public health and is recommended for immediate further study. Fortifying refined grain and drinking water with biologically available magnesium to pre-twentieth century levels is recommended.

Although the first report of magnesium treatment for agitated depression was published in 1921 showing success in 220 out of 250 cases, and there are modern case reports showing rapid terminating of TRD, only a few modern clinical trials were found. A 2008 randomized clinical trial showed that magnesium was as effective as the tricyclic anti-depressant imipramine in treating depression in diabetics and without any of the side effects of imipramine. Intravenous and oral magnesium in specific protocols have been reported to rapidly terminate TRD safely and without side effects. Magnesium has been largely removed from processed foods, potentially harming the brain. Calcium, glutamate and aspartate are common food additives that may worsen affective disorders. We hypothesize that – when taken together – there is more than sufficient evidence to implicate inadequate dietary magnesium as the main cause of TRD, and that physicians should prescribe magnesium for TRD. Since inadequate brain magnesium appears to reduce serotonin levels, and since anti-depressants have been shown to have the action of raising brain magnesium, we further hypothesize that magnesium treatment will be found beneficial for nearly all depressives, not only TRD.


Rapid recovery from major depression using magnesium treatment.

Source

George Eby Research, 14909-C Fitzhugh Road, Austin, TX 78736, USA. george.eby@coldcure.com

Abstract

Major depression is a mood disorder characterized by a sense of inadequacy, despondency, decreased activity, pessimism, anhedonia and sadness where these symptoms severely disrupt and adversely affect the person's life, sometimes to such an extent that suicide is attempted or results. Antidepressant drugs are not always effective and some have been accused of causing an increased number of suicides particularly in young people. Magnesium deficiency is well known to produce neuropathologies. Only 16% of the magnesium found in whole wheat remains in refined flour, and magnesium has been removed from most drinking water supplies, setting a stage for human magnesium deficiency. Magnesium ions regulate calcium ion flow in neuronal calcium channels, helping to regulate neuronal nitric oxide production. In magnesium deficiency, neuronal requirements for magnesium may not be met, causing neuronal damage which could manifest as depression. Magnesium treatment is hypothesized to be effective in treating major depression resulting from intraneuronal magnesium deficits. These magnesium ion neuronal deficits may be induced by stress hormones, excessive dietary calcium as well as dietary deficiencies of magnesium. Case histories are presented showing rapid recovery (less than 7 days) from major depression using 125-300 mg of magnesium (as glycinate and taurinate) with each meal and at bedtime. Magnesium was found usually effective for treatment of depression in general use. Related and accompanying mental illnesses in these case histories including traumatic brain injury, headache, suicidal ideation, anxiety, irritability, insomnia, postpartum depression, cocaine, alcohol and tobacco abuse, hypersensitivity to calcium, short-term memory loss and IQ loss were also benefited. Dietary deficiencies of magnesium, coupled with excess calcium and stress may cause many cases of other related symptoms including agitation, anxiety, irritability, confusion, asthenia, sleeplessness, headache, delirium, hallucinations and hyperexcitability, with each of these having been previously documented. The possibility that magnesium deficiency is the cause of most major depression and related mental health problems including IQ loss and addiction is enormously important to public health and is recommended for immediate further study.

30 SECONDS TO THE FOUNTAIN OF YOUTH

The time course of the human growth hormone response to a 6 second and a 30 seconds cycle ergo meter sprint.

High Intensity Exercise Exponentially Boosts Growth Hormone

Source

Department of Physical Education, Sports Science and Recreation Management, Loughborough University, UK.


The study also showed that the 30 second sprint raised HGH levels by up to 530% over the resting baseline.  Baseline is what your normal sedentary average resting hgH secretion is.


An exercise intensity above lactate threshold and for a minimum of 10 minutes facilitates a push secretion of hGH. Exercise exertion above the lactate threshold(With a higher exercise intensity the lactate level in the blood reaches the 'anaerobic threshold, the onset of blood lactate accumulation) intensifying the pulsatile release of hGH during the delta wave sleep cycle, increasing 24-hour hGH secretion.”

Abstract

Exercise is a potent stimulus for the release of human growth hormone (hGH)

The highest measured mean serum hGH concentrations after the 30 s sprint were more than 450% greater than after the 6 s sprint.

Repeated bouts of aerobic exercise within a 24-hour period result in increased 24-hour integrated GH concentrations. Because the GH response to acute resistance exercise is dependent on the work-rest interval and the load and frequency of the resistance exercise used, the ability to equate intensity across different resistance exercise protocols is desirable.

While exercise interventions may not restore GH secretion to levels observed in young, healthy individuals, exercise is a robust stimulus of GH secretion. The combination of exercise and administration of oral GH secretagogues may result in greater GH secretion than exercise alone in individuals who are older or have obesity. 

Dr. Colgan wrote an article in the 1990's that a full throttle 30 second sprint, would increase growth hormone 10 fold.

Monday, June 10, 2013

In 1992, the Swiss Health Service estimated that women consuming the equivalent of two cups of soy milk per day provides the estrogenic equivalent of one birth control pill. That means women eating cereal with soy milk and drinking a soy latte each day are effectively getting the same estrogen effect as if they were taking a birth control pill.






Researchers have identified a protein called zonulin that increases intestinal permeability in humans and other animals.7 This led to a search of the medical literature for illnesses characterized by increased intestinal permeability (leaky gut). Imagine their surprise when the researchers found that many, if not most, autoimmune diseases – including celiac disease,depression, type 1 diabetes, multiple sclerosis, rheumatoid arthritis and inflammatory bowel disease – are characterized by abnormally high levels of zonulin and a leaky gut.

several features of the modern lifestyle directly contribute to unhealthy gut flora:
Antibiotics and other medications like birth control and NSAIDs
Diets high in refined carbohydrates, sugar and processed foods
Diets low in fermentable fibers
Dietary toxins like wheat and industrial seed oils that cause leaky gut
Chronic stress
Chronic infections

In Step #1: Don’t Eat Toxins, I explained that one of the main reasons we don’t want to eat wheat and other gluten-containing grains is that they contain a protein called gliadin, which has been shown to increase zonulin production and thus directly contribute to leaky gut.

But what else can cause leaky gut? In short, the same things I listed above that destroy our gut flora: poor diet, medications (antibiotics, NSAIDs, steroids, antacids, etc.), infections, stress, hormone imbalances, and neurological conditions (brain trauma, stroke and neurodegeneration).



In fact, researchers have found that they can induce type 1 diabetes almost immediately in animals by exposing them to zonulin. They develop a leaky gut, and begin producing antibodies to islet cells – which are responsible for making insulin


That’s exactly what’s happening today. These four food toxins – refined cereal grains, industrial seed oils, sugar and processed soy – comprise the bulk of the modern diet. Bread, pastries, muffins, crackers, cookies, soda, fruit juice, fast food and other convenience foods are all loaded with these toxins. And when the majority of what most people eat on a daily basis is toxic, it’s not hard to understand why our health is failing.

Soy contains trypsin inhibitors that inhibit protein digestion and affect pancreatic function;
Soy contains phytic acid, which reduces absorption of minerals like calcium, magnesium, copper, iron and zinc;
Soy increases our requirement for vitamin D, which 50% of American are already deficient in;
Soy phytoestrogens disrupt endocrine function and have the potential to cause infertility and to promote breast cancer in adult women.
Vitamin B12 analogs in soy are not absorbed and actually increase the body’s requirement for B12;
Processing of soy protein results in the formation of toxic lysinoalanine and highly carcinogenic nitrosamines;
Free glutamic acid or MSG, a potent neurotoxin, is formed during soy food processing and additional amounts are added to many soy foods to mask soy’s unpleasant taste; and,
Soy can stimulate the growth of estrogen-dependent tumors and cause thyroid problems, especially in women.

First, the soy products consumed traditionally in Asia were typically fermented and unprocessed – including tempeh, miso, natto and tamari. This is important because the fermentation process partially neutralizes the toxins in soybeans


Because plants like cereal grains are always competing against predators (like us) for survival. Unlike animals, plants can’t run away from us when we decide to eat them. They had to evolve other mechanisms for protecting themselves. These include:
producing toxins that damage the lining of the gut;
producing toxins that bind essential minerals, making them unavailable to the body; and,
producing toxins that inhibit digestion and absorption of other essential nutrients, including protein.

How to maintain and restore a healthy gut

The most obvious first step in maintaining a healthy gut is to avoid all of the things I listed above that destroy gut flora and damage the intestinal barrier. But of course that’s not always possible, especially in the case of chronic stress and infections. Nor did we have any control over whether we were breast-fed or whether our mothers had healthy guts when they gave birth to us.

If you’ve been exposed to some of these factors, there are still steps you can take to restore your gut flora:
Remove all food toxins from your diet
Eat plenty of fermentable fibers (starches like sweet potato, yam, yucca, etc.)
Eat fermented foods like kefir, yogurt, sauerkraut, kim chi, etc., and/or take a high-quality, multi-species probiotic
Treat any intestinal pathogens (such as parasites) that may be present
Take steps to manage your stress

Selegiline a proven anti-anhedonia and neuroprotective agent.

Selegiline increases cellular levels of superoxide dismutase (one of the body's most potent anti-oxidant) by direct alteration of gene transcription synthesis.  The same kind of direct action on DNA, selegiline boosts nerve growth factors, proteins ceasing cell death.

With age ,m neurons decrease in number and MAO-B increases which breaks down neurotransmitters.  Every decade dopamine levels in the striatum  drop by 13%, contributing to parkinson's.

Selegiline can be obtained from alldaychemist.com.

Tuesday, June 4, 2013

Flush your Xanax, Pop Steriods and Sleep Like a Teenager...........Allopregnanolone affects sleep in a benzodiazepine-like fashion

Insomnia will be a thing the past you can happily forget about.  Scientific advancements in the arena of neurosteriods have proven  the potent power of allopregnanolone to flood the gamma amnio butyric acid receptors in the brain, inducing deep slow wave sleep.  The gamma amnio butyric acid receptors are the same ones the popular benzodiazepines target and act on to quell anxiety, anesthetize and sedate in even the worst cases of insomnia.

Allopregnanolone has numerous advantages over benzodiazepines and other pharmaceutical tranquilizers.   

Pregnenolone (allopregnanolone is a metabolite of pregnenolone and progesterone)

 Pros:  1. actually boosts cognitive performance, memory, learning, neurogenesis, neuroprotection and overall mood

2. generates the most restoring delta slow wave sleep, when growth hormone is released

3. increases brain levels of acetylcholine

Benzodiazepines, Ambien and tranquilizers
Cons:  1.  decrease  REM and delta wave sleep
2.  cause cognitive decline, memory loss
3.  long term use results in brain damage


The diagram above shows the hormonal cascade and synthesis of allopregnanolone.

Controlled double blind placebo research (cited and linked below) suggests that both progesterone and pregnenolone  both increase levels of allopregnanolone through oral or injected routes of administration.

 1997 Sep;282(3):1213-8.

Allopregnanolone affects sleep in a benzodiazepine-like fashion.

Source

Max Planck Institute of Psychiatry, Clinical Institute, Munich, Germany. lancel@mpipsykl.mpg.de


The sleep effects of allopregnanolone are very similar to those elicited by larger doses of progesterone, which produce comparable brain levels of allopregnanolone. These data indicate that the steroid allopregnanolone has benzodiazepine-like effects on sleep.  Recent research in rats and humans has shown that exogenous progesterone evokes a sleep profile similar to that induced by agonistic modulators of g-aminobutyric acid receptors, such as benzodiazepines. This finding suggests the involvement of the neuroactive metabolite of progesterone, allopregnanolone.

Both doses of allopregnanolone reduced the latency to non-rapid eye movement sleep (nonREMS) and 15 mg/kg allopregnanolone significantly increased the time spent in pre-REMS, an intermediate state between
non-REMS and REMS 

Steroid hormones affect neurotransmission in the brain. Data from animal experiments have shown that progesterone metabolites enhance the action of gamma-aminobutyric acid (GABA), the main inhibitory neurotransmitter in the cortex, producing benzodiazepine-like (e.g., diazepam and lorazepam) physiologic and behavioral effects.


Several lines of evidence indicate that the central-depressant action of progesterone is due not so much to the binding of progesterone to intracellular steroid receptors but rather is chiefly mediated by the action of its 5 alpha reduced metabolite 3a-hydroxy-5a-pregnan-20-one (allopregnanolone) at the membrane-bound GABAA receptors. Both endogenous and exogenous increases in the level of progesterone result in rapid elevations of allopregnanolone concentrations in plasma and brain (Barbaccia et al., 1996; Korneyev and Costa, 1996; Lancel et al., 1996b; Paul and Purdy, 1992). Electrophysiological and biochemical experiments showed that allopregnanolone is a potent allosteric agonistic modulator of GABAA receptors. In agreement with these findings in the rat, a dose of 300 mg of micronized progesterone given orally to male subjects has been shown to reduce non-REMS latency, to promote stage 2 sleep, to slightly suppress slow-wave sleep and to decrease EEG activity in the lower frequencies and enhance activity in the frequencies .15 Hz during nonREMS (Friess et al., 1997). Two observations suggest that allopregnanolone is implicated in the influence of progesterone on sleep. 

 The present data show that systemic administration of allopregnanolone mixed with oil produced rapid, long-lasting (.5 hr), seemingly dose-dependent increases in the levels of allopregnanolone in both plasma and brain. The present study shows for the first time that exogenous allopregnanolone significantly influences sleep. Both doses (7.5MG/KG AND 15MG/KG) tended to reduce non-REMS latency (table 1), which indicates a rapid hypnotic action. The higher dose significantly promoted pre-REMS, which occurred mainly during the first 2 postinjection hr.  The influence of allopregnanolone both on the amount of time spent in the different vigilance states and on EEG activity during non-REMS and REMS is reminiscent of the effects induced by benzodiazepines, which suggests that the influence of allopregnanolone on sleep is mediated by GABAA receptors. Nevertheless,the comparison of the sleep changes induced by allopregnanolone with those observed earlier after the administration of various doses of progesterone (Lancel et al., 1996b) shows that the overall effects of 15 mg/kg allopregnanolone are similar to those evoked by 90 mg/kg progesterone. As with the higher dose of allopregnanolone, 90 mg/kg progesterone shortened sleep latency, significantly increased the time spent in pre-REMS and was too low to suppress REMS or affect the number and average duration of the sleep episodes. The hypnotic effects of progesterone are to a large extent mediated by the positive allosteric interaction of its metabolite allopregnanolone with GABAA receptorsFrom the pharmacological point of view, steroids related to allopregnanolone, known as epalons, are likely to affect sleep in a benzodiazepine-like fashion. 

epalonsClass of neuroactive steroids. Name derived from epiallopregnanolone, an endogenous metabolite of progesterone that has activity on the GABA-A receptor complex. Have anxiolytic, anti-convulsant and sedative-hypnotic properties.

 Crit Rev Neurobiol. 1995;9(2-3):207-27.  A putative receptor for neurosteroids on the GABAA receptor complex: the pharmacological properties and therapeutic potential of epalons.  Gee KW, McCauley LD, Lan NC.
Source Department of Pharmacology, College of Medicine, University of California, Irvine 92717, USA. 

Abstract: A critical mass of evidence now supports the existence of a novel class of neuroactive steroids. These steroids are devoid of any known steroid hormone activity and have high specificity for the gamma-aminobutyric acidA receptor complex (GRC), which is a ligand-gated chloride channel that mediates the inhibitory action of the neurotransmitter gamma-aminobutyric acid (GABA). 
 These neuroactive steroids have anxiolytic, anticonvulsant, and sedative-hypnotic properties. Based upon some of the unique characteristics of the epalons relative to barbiturates and the BZs, it is plausible that the epalons can be developed into a novel class of therapeutic agents for the treatment of anxiety, epilepsy, and insomnia.




Editors note:  Pregnenolone and Progesterone should not be taken by anyone in their 20's unless blood and saliva tests show levels are below range, because this will prevent the body's own production of these hormones from cholesterol.  All hormones  applied by a creme, IV or injection will dodge the infamous first pass through the liver, greatly reducing bio-availability.  Make sure you always implement a liver detox (standardized milk thistle, dandelion, phosphatidyl choline) into your daily regimen if you plan on taking oral steriods, and have your liver functioning tested annually.