Showing posts with label Alzheimer's. Show all posts
Showing posts with label Alzheimer's. Show all posts

Saturday, February 8, 2014

Alzheimer's Gluten Acts Like A 'Brain Drug

Dramatic Recovery In Parkinson’s Patient with Gluten Free Diet


Dramatic Recovery In Parkinson's Patient with Gluten Free Diet
Could gluten's toxicity extend to the nervous system, producing symptoms identical to classical Parkinson's disease? A new case study adds to a growing body of research indicating that wheat's neurotoxicity is greatly underestimated.

A remarkable new case report describing the dramatic recovery of a 75-year-old Parkinson's disease patient after following a 3-month long gluten free diet reveals the need to explore whether there is an increased prevalence of silent or symptomatic celiac disease or non-celiac gluten sensitivity both in those afflicted with Parkinson's disease and the related multi-factorial neurodegenerative condition known as Parkinsonism.

Published in the Journal of Neurology, the report notes that celiac disease often manifests with only neurological symptoms, even in advanced age. This may strike the reader as surprising, considering gastrointestinal complaints are the most commonly noticeable symptom; and yet, when the voluminous published literature on gluten related adverse health effects is taken into account, so-called 'out of intestine' expressions of intolerance to gluten-containing grains are far more common than gut-related ones, with no less than 200 distinct adverse health effects implicated. You can read our summary of the biological carnage exacted by this 'king of grains' here: Wheat: 200 Clinically Confirmed Reasons Not To Eat It. You will notice that harm to the brain figures high on the list. From schizophrenia to mania, autism to peripheral neuropathy, the central nervous system is particularly sensitive to its adverse effects.

There are a wide range of mechanisms driving gluten associated neurotoxicity, such as
Gluten Acts Like A 'Brain Drug' The presence of pharmacologically active opioid peptides in wheat including four gluten exorphins and gliadorphin, and another is gluten's ability to restrict blood flow to the frontal cortex. Read More: "Do Hidden Opiates In Our Food Explain Food Addictions?"

Gluten Brain Autoimmunity Plenty of research now indicates that in susceptible individuals wheat adversely affects the gut-brain axis, increases intestinal permeability, and ultimately leads to the immune system misidentifying self-structures within the brain or neurological tissue as other, causing the host immune system to attack its own nervous system. Read More 2 Popular Foods May Turn the Immune Against the Brain."


Wheat's Invisible Thorns Affect The Brain The defensive carbohydrate-binding protein in wheat known as wheat germ agglutinin (WGA), also know as "wheat lectin," has been found to cross the blood-brain-barrier and can interfere with neurological function in a number of ways. Read more: Opening Pandora's Bread Box: The Critical Role of Wheat Lectin in Human Disease.
Grains Metabolically Impair the Brain The larger context is that grains provide an inappropriate or suboptimal set of nutrients for brain metabolism. Dr. David Perlmutter in his NY Times bestselling book Grain Brain links cognitive impairments endemic to older populations in Western cultures to the over consumption of carbohydrates (from grains and sugar), and the under consumption of fats.

You can also read Dr. Kelly Brogan's article "This Is Your Body and Brain on Gluten" to get greater perspective on the topic.

Considering these factors, it is not surprising that gluten removal from the diet could result in what the title of the published case report described as a "Dramatic improvement of parkinsonian symptoms after gluten-free diet introduction in a patient with silent celiac disease." We've seen similar remarkable recoveries with brain-metabolism optimizing fats like coconut oil in cases of debilitating dementia, including Alzheimer's disease.



In this new case study, the 75-year-old man presented with a 1-year history of "difficulty walking, instability, and fatigability. His neurological examination revealed:
Facial hypomimia reduced facial expressions
Bradykinesia extreme slowness of movements and reflexes
Rigidity
Postural instability

A brain scan was performed using Single-photon emission computed tomography (SPECT), revealing abnormalities consistent with low dopamine production and which in combination with the clinical data lead to a diagnosis of Parkinson's disease. Additional laboratory blood work revealed lower than normal level of serum folate, elevated homocysteine, with normal vitamin B12 levels. To assess the possibility of asymptomatic malabsorption due to a silent celiac disease further blood screening was explored. Anti-gliadin antibodies, markedly elevated IgA, anti-transglutaminase antibodies, and positive anti-endomysial antibodies – all signs of gluten associated autoimmunity. Finally, a duodenal biopsy was performed revealing intestinal characteristics flattened villi; crypt hyperplasiaconsistent with celiac disease. As a result, the gastroenterologist prescribed a gluten-free diet.

Remarkably, after only 3 months of abstinence from gluten, the patient reported an almost complete remission of symptoms, subsequently confirmed by a neurological evaluation. 18 months later he was reexamined and was found to have improved further.

Notably, the patient did not see measurable improvements in the dopaminergic abnormalities discovered in his brain scan, which would be expected in classical Parkinson's disease, which is marked by the degeneration of the dopamine producing cells in the substantia nigra of the brain. The authors therefore did not posit that the celiac disease caused Parkinson's disease in the patient, but rather that celiac disease exacerbated parkinsonism in this case. The case, however, does illustrate the possibility that a number of patients diagnosed with Parkinson's disease are suffering from previously unidentified and unreported gluten-associated Parkinsonism, which from the outside clinical presentation can look identical. Those folks, who would benefit greatly from removing the cause of the neurological problems  namely, gluten/wheat removal are often overdiagnosed and overtreated with drugs aimed at alleviating Parkinson's disease, but which ultimately can lead to accelerated degeneration of endogenous dopamine production in the brain, enhanced neurotoxicity due to drug metabolites (e.g. 6-hydroxydopamine), and the production of dyskinesias (movement disorders) that are far worse than, or were never present within, the pre-treatment condition.

For additional research related to natural interventions for Parkinson's disease, use our database:Parkinson's Disease Research. Also, our section on neurodegenerative diseases provides additional help: Neurodegenerative Disease Research.

Vincenzo Di Lazzaro, Fioravante Capone, Giovanni Cammarota, Daniela Di Giuda, Federico Ranieri.Dramatic improvement of parkinsonian symptoms after gluten-free diet introduction in a patient with silent celiac disease. J Neurol. 2014 Feb ;261(2):443-5. Epub 2014 Jan 25. PMID:24464413

Sunday, September 29, 2013

Alzheimer's

How to Prevent Alzheimer’s Disease A Neurologist Speaks Out

Alzheimer's disease is at epidemic proportions, with 5.4 million Americans including one in eight people aged 65 and over living with the disease In the next 20 years, it is projected that Alzheimer's will affect one in four Americans, rivaling the current prevalence of obesity and diabetes.

There is still no known accepted cure for this devastating disease, and no effective treatments. Alzheimer's drugs are often of little to no benefit at all, which underscores the importance of prevention throughout your lifetime.

Fortunately, Alzheimer’s prevention is actually easier than you might think. There’s exceptionally compelling research showing that your brain has great plasticity, which you control through your diet and lifestyle choices.

Here, Dr. David Perlmutter probably the leading natural medicine neurologist in the US, from my perspective shares his insights into this pervasive problem. I don’t know anyone who exceeds his level of expertise in traditional neurology and still shares the same philosophical orientation that I have.

He has a clinic in Naples, Florida, and he’s been very active in publishing his findings in peer-reviewed medical journals. He’s also a fellow of the American College of Nutrition, .


I have a very strong background in traditional neurology, Dr. Perlmutter says. As a neurologist for many years, I became more and more frustrated with our lack of ability to actually treat diseases. We were really only treating symptoms.


When I finally began to understand what the proximate cause of the various illnesses we were dealing with was, I realized that mainstream neurology, though I don’t want to sound too critical, really pays no attention to the causation part of the story.
The Role of Grains in Disease Propagation


He realized an answer would never become apparent by simply writing prescriptions and hoping for the best. Instead, he began investigating the role of nutrition on brain health. Alzheimer’s, according to the RAND Corporation, is currently costing us some $200 million a year, yet it is largely preventable. And virtually no one talks about that!


This is a disease that is highly revenue-producing for mega factories of various so-called Alzheimer’s drugs, Dr. Perlmutter says. The point is there is no meaningful treatment in 2013. It is a disease predicated on lifestyle choices primarily, because of the high amount of carbohydrates/sugar that we now, as Western-culture individuals, are consuming.


It’s a preventable disease
. It surprises me at my core that no one’s talking about the fact that so many of these devastating neurological problems are, in fact, modifiable based upon lifestyle choices.

Dr. Perlmutter specifically looked at the impact of gluten and casein, or wheat and dairy primarily, on autoimmune diseases. His New York Times Bestseller, Grain Brain, reveals his findings, the cornerstones of which are the powerfully toxic role of glucose sugar and carbohydrates in one's diet.

He also stresses that gluten sensitivity is involved in most chronic disease, including those affecting the brain, because of how gluten affects your immune system. Unfortunately, many people, physicians included, still believe that if you don’t have celiac disease, gluten is fair game and you can eat as much of it as you like.

Full-blown Celiac disease, which is gluten sensitivity affecting your small intestine, affects an estimated 1.8 percent of people in Western cultures. But gluten sensitivity may actually affect as much as 30 to 40 percent of all people, and according to Dr. Alessio Fasano at Massachusetts General Hospital, virtually all of us are affected to some degree.

This is because we all create something called zonulin in the intestine in response to gluten. This protein, found in wheat, barley and rye, makes your gut more permeable, which allows proteins to get into your bloodstream that would otherwise have been excluded. That then sensitizes your immune system and promotes inflammation and autoimmunity. This kind of gut permeability is also promoted by things like antibiotics and chlorinated water.
The Gut-Brain Connection is Critical to Understand


Once gluten sensitizes your gut, it then becomes more permeable and all manner of previously excluded proteins including casein and other dairy proteins have direct access to your bloodstream, thereby challenging your immune system.


They’ve been talking about it for years and years which is now just gaining traction in mainstream medicine)that our health really depends on maintaining a barrier of the intestine from the bloodstream, Dr. Perlmutter says.


We now understand that the so-called blood-brain barrier, or that barrier that keeps things out of the brain where they don’t belong, is also affected by gluten, according to new research. It’s a very exciting time when we recognize that our biggest exposure to the environment is actually the lining of our intestines  not our lungs, not our skin. We are in fact very much dependent on the microbiota, the bacteria living in the gut, to maintain our health.”

According to Dr. Perlmutter, much of our current disease burden stems from the fact that we are contaminating our immune systems with proteins to which the human immune system has never, in the history of humankind, been previously exposed to. While not discussed in this interview, a MAJOR factor is the development of genetically engineered (GE) grains, which are now pervasive in most processed foods sold in the US. These GE crops create proteins never before encountered in any natural grain or food, so GE grains deliver a double-whammy against your immune system. Food allergies clearly appear to be one of the most noticeable side effects of a GE-grain diet.


We recognize that food is far more than protein, carbohydrates, fat, and micronutrients, and that food really does represent information. The foods that we consume are instructing our genes. Therefore, that’s a very empowering notion: you can change your genetic destiny based upon the food choices that you make, Dr. Perlmutter says.

Dr. Natasha Campbell-McBride, another neurologist who has also done remarkable work in this area as a result of seeking a solution for her autistic son, came to the same conclusion discussed by Dr. Perlmutter. Essentially, preventing and treating neurological disorders requires severe restriction of gluten and casein. You also need to address your gut flora.


With specific response to your comments about autism, we do know that some of the milk-related proteins tend to lead to antibody production in the brains of autistic children, blocking what’s called the folate receptor, Dr. Perlmutter says. One of the propositions is that there’s this blockage of the ability of folate to get into the brains of certain children, and this leads to all kinds of cognitive and neurocognitive issues.


The State University of New York has actually developed a screen for looking at folate receptor antibodies. We have found that to be actually very helpful. It’s a very exciting time for those of us not just in neurology but in all branches of medicine, who are suddenly realizing that we've come full circle. We’re now back to understanding that nutrition plays a pivotal role in the health of humans.
Avoiding Dairy Does NOT Include Avoiding Dairy Fats


I believe it would be wise for most people to avoid pasteurized dairy primarily casein but also other proteins and gluten. That said, there are subgroups of people who are particularly prone to harm from these proteins, and as a rule must avoid them in order to maintain their health. Bear in mind that dairy fat like butter, which has virtually no protein, is not problematic and can be consumed even by those who are sensitive to milk proteins. As stated by Dr. Perlmutter:


We need to eat fat. We’re suggesting a revolutionary dietary change, telling people they should go on this new diet which is only the diet humans have eaten for the past 2.6 million years! We've always eaten fat. Fat is the most wonderful health-providing food that we can obtain in the human diet. Of course, we have to qualify that with what type of fat you are eating.

Beneficial health-promoting fats that your body and your brain in particular needs for optimal function include organic butter from raw milk, clarified butter called organic grass fed raw butter, olives, organic virgin olive oil and coconut oil, nuts like pecans and macadamia, free-range eggs, wild Alaskan salmon, and avocado, for example.

According to Dr. Perlmutter, our current dietary fat phobia has absolutely been the cornerstone of our most common degenerative diseases of the day, including Alzheimer’s. Why? Because when you cut dietary fat and keep protein about the same, you’re going to fill in the gaps with health-harming carbohydrate foods, predominantly grains.


This whole grain goodness, as the US Department of Agriculture is trying to convince us we should focus on in terms of our dietary choices, is the cornerstone of our most devastating diseases. I mean, brain diseases like Alzheimer’s, cardiovascular disease, and obviously, what leads to them, diabetes, which is so prevalent in Western societies. Again, it’s the getting away from fat and the substitution with wheat- and corn-based carbohydrate high-fructose corn syrup that really, in my opinion, explains this huge explosion of degenerative conditions that are crippling us medically and crippling us economically as well, he says.


But the quality of the fat that we consume is absolutely fundamental. When we’re saying high-fat diet, we’re not talking about prepared foods on the Twinkie aisle at the grocery store that contain modified trans fats; hydrogenated fats that are clearly coffin nails. They’re a great risk for brain disorders, heart disorders, diabetes, etc. We’re talking about these beautiful, natural fats that we have been consuming for more than two million years.
Recommended Tests to Evaluate Disease Risks


There are specific tests that can help you determine your level of sensitivity to dairy proteins like casein, as well as gluten. The most effective test for gluten sensitivity, according to Dr. Perlmutter, is a test called the Cyrex Array 3 test. Most laboratories, when you order a test for either gluten sensitivity or celiac disease specifically, will look for antibodies against just one type of gliadin. However, there are dozens of different types of gliadin that can incite immune reaction or immune reactivity. The Cyrex test looks at 24 different parameters of gluten sensitivity, which gives you a much clearer picture.


Most commonly when I’m seeing patients, they’ve already had some form of preliminary gluten sensitivity test which was negative, and we find [out the truth] by doing the Cyrex test, he says.

The same lab offers another test, Cyrex Array 4, which looks at cross-sensitivity in people who are gluten-sensitive. This test includes a dairy product panel as well as amaranth, spelt, quinoa, rice, coffee, chocolate, and other foods that may be cross-reactive with respect to gliadin. Two other tests recommended by Dr. Perlmutter that are potent predictors of Alzheimer’s disease specifically are:
Fasting blood sugar, as this is a powerful predictor of your risk for Alzheimer’s disease. In this interview, he discusses research showing a very direct correlation between your fasting blood sugar and the rate at which your brain shrinks. The higher your fasting blood sugar, the greater your risk. Interestingly, brain shrinkage occurs at blood sugar levels that are currently considered within the normal range (90-100), and even small elevations of blood sugar directly correlate to increased risk for having shrinkage of your hippocampus, your memory center, which is the hallmark of Alzheimer’s disease.
Hemoglobin A1c. This is a marker of your average blood sugar over about a three-to four-month period of time. Again, there’s a striking correlation between hemoglobin A1c and the rate at which your brain is shrinking.

Both of these factors, your blood sugar and hemoglobin A1c, are entirely within your power to control, as they respond to dietary changes. Quite simply, you lower them by reducing your carbohydrate consumption. As stated by Dr. Perlmutter:


You can absolutely control your blood sugar. It’s a lifestyle choice. Do you eat grain? Do you drink orange juice in the morning? Are you having cereal in the morning? Have you decided to go low-carb and high-fat? In the latter case, your hemoglobin A1c will come down, your fasting blood sugar will come down, and lo and behold, you have taken positive steps to reduce your risk of brain shrinkage.
How the Science of Neuroplasticity Changes the Game


It’s important to realize that, despite what the media tells you, your brain is not programmed to shrink and fail as a matter of course as you age. We now know that every activity in which you engage be it exercise, the foods you eat, the supplements you take, your personal relationships, your emotional state, your sleep patterns all of these factors dramatically influence your genetic expression from moment to moment. Any given gene is not in a static on or off position. Neither are the deterministic. You may be a carrier of a gene that never gets expressed, simply because you never supply the required environment for it to turn on.


We interact with our genome every moment of our lives, and we can do so very, very positively, Dr. Perlmutter says. Keeping your blood sugar low is very positive in terms of allowing the genes to express reduced inflammation, which increase the production of life-giving antioxidants. So that’s rule number one: You can change your genetic destiny.


Rule number two: you can change your genetic destiny to grow new brain cells, specifically in the hippocampus. Your brain’s memory center regenerates. You are constantly growing new brain cells into your 50s, 60s, 80s, and 90s  throughout your lifetime  through a process called neurogenesis.


That said, these two ideas come together because you can turn on your genes through lifestyle choices that enhance neurogenesis and that enhance regrowth of cells and expansion of your brain’s memory center. This was proven by researchers recently. They demonstrated that there are factors under our control that can make that happen.

Lifestyle strategies that promote neurogenesis and regrowth of brain cells include the following. All of these strategies target a specific gene pathway called BDNF or brain-derived neurotrophic factor, which promotes brain cell growth and connectivity as demonstrated on MRI scans.
Exercise. In one year-long study, individuals who engaged in exercise were actually growing and expanding the brain’s memory center one to two percent per year, where typically that center would have continued to decline in size.
Reducing overall calorie consumption
Reducing carbohydrate consumption
Increasing healthy fat consumption
Increasing your omega-3 fat intake and reducing consumption of damaged omega-6 fats think processed vegetable oils in order to balance your omega-3 to omega-6 ratio. I prefer krill oil to fish oil here, as krill oil also contains astaxanthin, which appears to be particularly beneficial for brain health. As explained by Dr. Perlmutter, it belongs to the class of carotenoids, and is very focused on reducing free radical-mediated damage to fat, and your brain is 60 or 70 percent fat
The Importance of Vitamin D and Cholesterol for Brain Health


Vitamin D also plays a fundamental role in brain health, immune function, and inflammation. According to Dr. Perlmutter, vitamin D influences the expression of more than 913 genes. Sadly, a vast majority of people are dramatically deficient in this critical steroid hormone, in large part because they've been fooled into fearing sun exposure. You've also been deceived into fearing cholesterol, which is another critical component of health.


Obviously, sunshine makes vitamin D in your body from some precursor. When I ask my patients what is that precursor, nobody seems to know. I tell them it’s this horrible thing called cholesterol, and their eyebrows go up, he says.Cholesterol is so drastically important for health, because  it’s the precursor for which you make vitamin D and it’s a fundamental compound of every cell in your body and made by every cell in your body. It’s a brain antioxidant. It’s a precursor for all the steroid sex hormones  it’s fundamentally important.

According to Dr. Perlmutter, research shows that elderly individuals with the lowest cholesterol levels have the highest risk for Alzheimer’s. They also have the highest risk for dying. As he says, the war on cholesterol is fundamentally inappropriate and harmful.


I say to my audiences very frequently, If cholesterol is so bad, what you’re saying is that if you believe in evolution or if you believe in creation  either way  either nature got it wrong or God got it wrong by putting the ability to make cholesterol in every one of our cells. Why would that be a mistake?


It’s not a mistake. We are desperate for cholesterol. It’s a fundamental player in every cell membrane. We've been on a high-cholesterol diet for millions of years, and it has served us well. In fact, our genome has been selected based upon that diet, being on a high-cholesterol diet eating eggs, animal fat, and animal protein.”
The Benefits of Fasting


Dr. Perlmutter places most of his patients on a ketogenic, high-fat, low-carbohydrate diet that is gluten-free, along with prescribed aerobic exercise. Certain supplements may also be used, especially if the patient is vitamin D deficient or has any other critical deficiency.

I've previously interviewed Dr. Seyfried, who is a researcher at Boston University and connected with Harvard. He was one of the leading investigators to adopt the ketogenic diet for a neurological condition, the treatment of seizures, and then from there started investigating its use for treatment of cancer. Another PhD, Dr. D’Agostino in Florida, is also doing similar work in this area.

It’s interesting to note that it all stemmed from the treatment of intractable seizure disorders; before they realized that it was also a potent treatment adjunct for cancer patients. Most interestingly, cancer cells do not have the ability to any significant degree to metabolize fat and are almost completely dependent on metabolizing sugar. When you go on a ketogenic diet, you effectively deprive the cancer cells of sugar, which starves them, while allowing normal cells to thrive. Beyond that, you also need to recognize that the balance of organisms in your intestine play a critical role in maintaining your immunity. Clearly, if you’re fighting disease of any kind, you want your immune system to function optimally.


When you damage your microbiom, the balance of bacteria, in your gut by taking chemotherapy, at the very least add in an aggressive probiotic approach to keep bad bacteria count healthy, Dr. Perlmutter says.

I’m particularly fond of using fermented vegetables, because they can deliver extraordinarily high levels of beneficial bacteria. Most people aren't aware that in a healthy serving of sauerkraut  two to three ounces or so  you’re getting the equivalent of nearly 100 capsules of the highest-potency probiotic you can buy. It’s clearly one of the most cost-effective alternatives. Furthermore, if it’s fermented with a starter culture, which we’re going to be offering soon, you can also get very high levels of vitamin K2, which is crucial to balance vitamin D.

Dr. Perlmutter also highly recommends fasting. Contrary to popular belief, the ideal fuel for your brain is not glucose but ketones, which is the fat that your body mobilizes when you stop feeding it carbs and introduce coconut oil and other sources of healthy fats into your diet. A one-day fast can help your body to reset itself, and start to burn fat instead of sugar. As part of a healthy lifestyle, I prefer an intermittent fasting schedule that simply calls for limiting your eating to a narrower window of time each day. By restricting your eating to a 6-8 hour window, you effectively fast 16-18 hours each day. To learn more, please see this previous article.


The easiest way to become ketotic is just to stop eating. Because if you go through your sugar stores and then your glycogen stores relatively soon, you begin to burn fat, the most incredibly powerful source of fuel for human physiology and especially for the brain,” he says.


To learn more, I highly recommend Dr. Perlmutter’s New York Times Best Selling book, Grain Brain. You can also find more information on his web site, DrPerlmutter.com, or on his Facebook page, which he posts to every day, highlighting recent research and upcoming conferences and lectures. You can also find more tips and guidelines in this previous article on Alzheimer’s prevention.



These changes that people can make in their diets are not draconian,” he says. The only thing that makes it difficult is because of what we are told by society we should be eating. Those statements are not given to us with good, sound scientific backing. Again, these are simple but profound choices that people can make.”

I couldn't agree more. Applying the strategies discussed in this interview and article can dramatically reduce your risk of succumbing to Alzheimer’s and other chronic diseases. Overall, it will also raise your general quality of life. Clearly, prevention is much easier than treating it after the fact. And even though there is this element of neuroplasticity, it’s far better to prevent brain degeneration to begin with. As Dr. Perlutter says


The time to fix the roof is when the sun is shining. That’s the segment of the population I really want to target  people who have not yet had cognitive issues but are at risk, which is basically all of us. In fact, this is the time to make the changes while you’re still healthy. Time to cut back on the carbohydrates, increase your consumption of good fats, get out and exercise. these are the fundamentals that could keep these problems from happening in the first place.


Docosahexaenoic acid

Docosahexaenoic acid is an omega-3 fatty acid that is a primary structural component of the human brain, cerebral cortex, skin, sperm, testicles and retina. 

DHA is the most abundant omega-3 fatty acid in the brain and retina. DHA comprises 40% of the polyunsaturated fatty acids (PUFAs) in the brain and 60% of the PUFAs in the retina. Fifty percent of the weight of a neuron's plasma membrane is composed of DHA. DHA is richly supplied during breastfeeding, and DHA levels are high in breast milk regardless of dietary choices.

DHA modulates the carrier-mediated transport of choline, glycine, and taurine, the function of delayed rectifier potassium channels, and the response of rhodopsin contained in the synaptic vesicles, among many other functions.

DHA deficiency is associated with cognitive decline. Phosphatidylserine (PS) controls apoptosis, and low DHA levels lower neural cell PS and increase neural cell death. DHA levels are reduced in the brain tissue of severely depressed patients.


Monday, September 23, 2013

Magnesium Alzheimer's

Magnesium Compound Reverses Neurodegeneration

Aged people are in the midst of an escalating Alzheimer's epidemic.1,2 It is now the sixth leading cause of death in the United States.

The horrific progression of Alzheimer's disease from dementia to personal extinction afflicts between 24-30 million people worldwide.4 Americans account for approximately one-fifth of those cases, which are expected to triple by 2050.3,6

While there is no cure for Alzheimer's, there is new hope thanks to the work of a team of researchers at Massachusetts Institute of Technology 

These scientists have identified several correctable factors involved in Alzheimer's onsetand a novel nutritional intervention that may effectively target them.

In this article, you will learn of the vital role that magnesium plays in protecting the aging brain's structure and function and why conventional supplements don't deliver enough magnesium into the brain.

Researchers have found that a new highly absorbable form of magnesium called magnesium-L-threonateconcentrates more efficiently in the brain, rebuilds ruptured synapses, and restores the degraded neuronal connections observed in Alzheimer's disease and other forms of memory loss.

In experimental models, magnesium-L-threonate induced improvements of 18% for short-term memory and 100%for long-term memory.8 Magnesium Deficiency: An Overlooked Cause of Neurologic Decay

Half of all aging individuals in the developed world are magnesium deficient, a nutritional deficit that worsens over time.

Confirmatory data show that Americans are no exception. For instance, American women consume just 68% of the recommended daily intake of magnesium.

Magnesium has long been known as a key nutrient for optimal brain function. More recently, scientists have found it specifically promotes learning and memory as a result of its beneficial effect on synaptic plasticity and density.

Magnesium works with calcium to modulate ion channels that open in response to nerve impulses, which in turn trigger neurotransmitter release. The most important of those channels is controlled by a complex called the NMDA receptor.13,14 NMDA receptors play an important role in promoting neural plasticity and synaptic density, the structural underpinnings of memory.15-17

Magnesium deficiency can cause symptoms ranging from apathy and psychosis to memory impairment.13,18 Insufficient magnesium slows brain recovery following injury from trauma and in laboratory studies accelerates cellular aging.

Ominously, magnesium deficiency may produce no overt symptoms in its initial stages.

Part of the problem is that it is difficult for the body to maintain sufficiently high concentrations of magnesium in the brain.8

For this reason, researchers have long sought ways that higher magnesium brain concentrations might be achieved and sustained.
A Breakthrough Form of Magnesium



Scientists have been challenged to find a way to raise magnesium levels in the brain. Even intravenous infusions cause only a modest elevation of magnesium levels in the central nervous system.

An innovative team of researchers from the Massachusetts Institute of Technology(MIT) recently found a way to surmount this obstacle. They formulated a new magnesium compound called magnesium-L-threonate or MgT that in lab tests allows for oral administration while maximizing magnesium loading into the brain.

Based on prior research, they meticulously documented that increased levels of magnesium in the brain promote synaptic density and plasticity in the hippocampus. Up until now, however, no widely available forms of magnesium met the criteria needed for rapid absorption and efficient transfer into the central nervous system.

By contrast, MgT yielded compelling results.

MgT oral supplements increased magnesium levels in spinal fluid, an index of measurement in brain magnesium by about 15%, while none of the other magnesium compounds tested produced significant elevations.8 While a 15% increase may not sound like a lot, it induced a profound effect on neurological function.

To evaluate the effects of MgT on memory, the researchers tested it against currently available magnesium compounds. They used a simple assessment of learning and memory called the Novel Object Recognition Test or NORT. A high NORT score means that the animal is good at recognizing and identifying new objects, a skill that is critical in aging humans as well.8 NORT is a good test of function in the hippocampus, which is rich in the NMDA receptors so closely controlled by magnesium.23

The researchers put aged animals through the NORT test, supplementing them with MgT or one of the commercially available magnesium compounds. Only MgT significantly enhanced both short- and long-term memory, boosting scores by 15% for short-term memory and 54% for long-term memory compared to magnesium citrate.8
Better Function of Memory-Forming Synaptic Connections

Given the effect of MgT in increasing synaptic density and plasticity in experimental animals rats, the research team asked the obvious next question, "Do those changes lead to an increase in the number of neurotransmitter release sites, and, subsequently, to enhanced signal transmission?" That, after all, is the hallmark of learning and memory.

Using high-tech microscopic measuring devices, the team demonstrated that the magnesium elevation in brain tissue observed in MgT supplementation increases the number of functioning neurotransmitter release sites.8 This effect could be likened to increasing the number of soldiers on the battlefield: when the call to action comes, a much larger force is prepared to perform.

The final question to be addressed in this series of studies was whether the increased density of synaptic connections directly correlated with the observed improvements in memory created by MgT supplementation.

The researchers systematically plotted out the time-course of the increase in synaptic density following MgT supplementation, and found that it directly paralleled the improvements in memory.8 They also found that when MgT supplementation was stopped, the density of synaptic connections dropped back to baseline, further confirming the correlation. They found that MgT supplementation boosted all of the animals' performance, not just average performance.
Improvement in Spatial Short-Term Memory

Spatial working memory is an essential memory function, helping you remember where things are and where you are in relation to the world over the short term. It is working memory that enables you to find your car keys as you head out the door or return to the correct page in the magazine you were reading a few minutes ago.

The MIT researchers tested spatial working memory in experimental animals. Without treatment, both young and old animals forgot the correct choice about 30% of the time. After 24 days of MgT supplementation, however, both young and old animals had improved this measurement of memory performance by more than 17%.8

Even more impressive, by 30 days of supplementation, the older animals' performance became equal to that of their younger counterparts. Since the older animals were more forgetful at baseline than the younger animals that meant that the older animals had a larger percentage memory improvement (nearly 19%) than the younger animals' more modest 13%.8

When MgT supplementation was suspended, the memory-enhancing effects persisted in younger animals, but in older animals spatial working memory performance declined dramatically, returning to baseline within 12 days.8 When MgT supplementation to the older animals was resumed, however, their memory performance was restored in 12 days.

In other words, magnesium-L-threonate improved memory in both old and young animals, but had a substantially greater effect on aged individuals—the very ones most in need of memory enhancements.

NOVEL MAGNESIUM COMPOUND HALTS NEUROLOGIC DECAY



Levels of Alzheimer's disease and associated memory loss among aging Americans are reaching epidemic levels.
The neurodegenerative processes involved in memory loss results from deterioration of connectivity between brain cells but are not a "natural function" of aging.
Low magnesium status can accelerate brain cell aging and memory loss.
Standard magnesium offers limited protection to brain cells.
Magnesium-L-threonate is a new form of magnesium that dramatically boosts levels of magnesium in the brain.
Boosting brain magnesium with magnesium-L-threonate enhances synaptic density and plasticity, the structural basis of learning and memory.
In numerous experimental models, supplementation with magnesium-L- threonate has been shown toenhance memory and cognitive performance in multiple tests.

Enhanced Spatial Long-Term Memory

Long-term spatial memory is crucial for older individuals. It's how you remember where you live or how to get to the grocery store. Loss of spatial long-term memory is one of the main reasons that older people with dementia get lost running even simple errands.

To test spatial long-term memory in MgT-supplemented animals, the researchers used a maze that required the animal to swim and find a submerged platform on which to rest. Again, both old and young animals supplemented with magnesium-L-threonate learned significantly faster than untreated animals during the training sessions.8



One hour after the training period, the researchers removed the submerged platform, causing the animals to have to search for its last location. Both young and old supplemented and unsupplemented animals remembered where the platform had been over the short term and were searching for it in the correct quadrant of the maze.

But after 24 hours, a remarkable difference was observed. Untreated animals, both young and old, completely forgot where the platform had been hidden, randomly searching in all quadrants of the maze. Supplemented animals, on the other hand, continued to search in the correct part of the maze more than twice as long as they looked in incorrect areas.8 That translated into improvements in spatial long-term memory of 122% in younger supplemented animals, and nearly 100% in older supplemented animals.

In short, MgT supplementation doubled the accuracy of long-term spatial memory in older animals, and more than doubled it in younger animals.
Better Recall

One critical memory function is the ability to bring up an important memory based on only partial information, a function called pattern completion.8 You use pattern completion memory to find your way around a familiar neighborhood after dark or following a heavy snowstorm. In both cases, some familiar cues are gone, but a healthy brain will fill in the missing details by completing a recognizable pattern.

As decsribed on the previous page, when researchers removed some of the external visual cues from the water maze, younger animals had no particular difficulty finding their way to the hidden platform during the first 24-hour period. Older animals, on the other hand, demonstrated substantial impairment when familiar cues were missing, spending more than twice as much time searching for the missing platform. When given MgT for 30 days, however, older animals performed as well as the younger ones, quickly finding the platform even when many of the external cues were unavailable.8

In human terms, this kind of improvement could mean the difference between a routine trip to the grocery store at dusk versus getting lost in the dark.

Having successfully demonstrated that magnesium-L-threonate (MgT) improves multiple forms of learning and memory in living animals, the research team sought to explore the cellular and molecular basis of that improvement. They wanted to understand in a detailed fashion just what changes the MgT was producing in the brains of older animals that helped them form stronger, more stable memories.

What they determined was compelling.


Increased Brain Cell Signaling

The first step was to determine the effects of MgT supplementation on signaling between brain cells mediated by what are known as NMDA receptors. These receptors operate through varying concentrations of calcium and magnesium in brain tissue, making them a logical point of observation.

The first finding was that MgT treatment in animals resulted in stronger signaling at essential brain cell synapses.8 This increase in signaling was accomplished by a 60% increase in production of new NMDA receptors and by increases of up to 92% in related proteins that play essential supporting roles in brain signal transmission.8
Higher Memory- Forming Synaptic Plasticity and Density

Synaptic plasticity, or the ability to rapidly change the number and strength of brain cell synapses, is critical to the brain's ability to form, retain, and retrieve memories. The research team compared synaptic plasticity in the brains of MgT-supplemented animals versus controls.8

They found that production of a very special subunit of the NMDA receptor, one closely associated with synaptic plasticity, was selectively enhanced by MgT supplementation.8 This molecular change is known to cause potent long-term increases in synaptic strength, and hence a greater capacity for information storage and memory.8,24-26

The result of these increases in NMDA receptor numbers was a 52% enhancement in long-term potentiation,8 which is the cellular equivalent of memory formation in the brain tissues of MgT-supplemented animals.27,28

Memory depends not only on synaptic plasticity, but also on the healthy physical structure of synapses between brain cells. Unfortunately, synaptic connections in the memory-rich hippocampus region of the brain decline with aging, which directly correlates with memory loss.8,29,30,31

One of the most vital structures to be found at brain cell synapses is the synaptic bouton, from the French word for button. When an electrical impulse reaches a pre-synaptic bouton, and ample calcium and magnesium are present, neurotransmitters are released to transmit the impulse to the next neuron in line. The greater the number and density of synaptic boutons, the stronger the electrochemical signal that the synapse can produce, and the more sustained the memory that is created.32

When the researchers examined the brains of control and MgT-supplemented animals under a high-power microscope, they readily detected much greater densities of synaptic bouton proteins in tissues from the supplemented animals. Those proteins are essential for neurotransmitter release in the several regions of the hippocampus vital for memory formation and retrieval.8 Remarkably, the density of the synaptic boutons was closely correlated with the memory performance of each individual animal on the novel object recognition test.

MECHANISMS OF BRAIN AGING AND MEMORY LOSS


Every memory you have, even those you've lost, produces physical changes in your brain. Memories form and are stored in multiple brain regions, but the most active and essential area is the hippocampus, a small, sea horse-shaped structure deep in the center of your brain.

Hippocampal memory enables you to recognize and distinguish between old friends and new acquaintances, or to find your way around a well-known floor plan. It is also used to comprehend and navigate new experiences based on old ones.

This puts the hippocampus squarely at the center of your ability to assimilate new information and integrate it with what you already know. As you learn and experience new events, cells in your memory centers tighten and enhance their neuronal connections, known as synapses.35

The ability of brain cells to quickly form new synapses and remove old ones is referred to as neurologic plasticity. Large numbers of synapses, and a high density of specialized synaptic structures called boutons, promote rapid retrieval and processing of the information stored by connected cells.36 In essence, neuronal plasticity is the physical equivalent of learning, while synaptic density is roughly the equivalent of memory.

Young brains exhibit high levels of neurologic plasticity that produce large numbers of interconnected synapses. That's why young people learn quickly and have strong memories.

With aging, however, the numbers of synapses, and the ability to rapidly form new ones, steadily declines. And that's just in normal aging. People with Alzheimer's disease, or its precursor, mild cognitive impairment MCI experience more rapid loss of both plasticity and synaptic number. And that's when memories begin to fade, or worse, to be lost entirely.

Since time immemorial, people have suspected that specific nutrients can positively affect cognitive functions such as learning and memory. It's now known that many nutrients can actually modify aging brain function, in part by increasing formation of brain synapses.

Magnesium has been established as having a positive impact on both neural plasticity and synaptic density.

Near-Term Research

The MIT team is rapidly putting in place two human studies of MgT on memory function, with results expected in the near future. Meanwhile, they have recently discovered several new roles for MgT in managing memory, in this case unwanted memories of the kind associated with post-traumatic stress disorder (PTSD).

Fear memories are expressed in response to objects or events previously linked with a potential danger. Over time, fearful reactions can dissipate when the triggering event is experienced in a safe environment.

Animal studies reveal that MgT enhances this process, so that events which previously caused an emotional response no longer trigger fear. MgT helps the pre-frontal region of the brain block the return of old fear memories.

Research reveals that MgT works by enhancing neural plasticity in the hippocampus and prefrontal cortex. These findings led the researchers to recommend that elevating brain magnesium with MgT be used to dampen traumatic memories and treat PTSD, anxiety, and depression.
Summary

Levels of Alzheimer's disease and associated memory loss among aging Americans are reaching epidemic levels.

The neurodegenerative processes involved in memory loss result from deterioration of connectivity between brain cells but are not a natural function of aging. Memory loss is now known to be associated with loss of synaptic density and plasticity in the brain. Low magnesium levels may contribute to such losses.

Magnesium-L-threonate (MgT), a new magnesium compound, boosts brain magnesium levels better than standard supplements. Studies reveal that MgT produces dramatic increases in synaptic density and plasticity, resulting in similar improvements in memory function itself.


I have been personally testing on myself Bud Karas and can tell great memory improvement


Wednesday, September 18, 2013

Alzheimer's

A stop motion video  about Alzheimer's at the School of Arts in Utrecht, Netherlands.


This disease in my opinion can be cured with relative ease Bud Karas 
here is just a small sample of what i will be teaching regarding these type of Brain disorders 

 Rosemary can enhance overall quality of memory as well as secondary memory factors on  Alzheimer's disease,

Acetylcholine  is present in Rosemary