Dr Andrew Weil on Glutathione and Parkinsons Disease. | Buy Glutathione Suppositories 500mg

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Q
A New Approach to Parkinson’s?
My husband has Parkinson’s disease. We have heard that the results of intravenous glutathione therapy are nothing short of amazing. Do you recommend that we check into this therapy?

A
Answer
Parkinson’s disease is a neurological disease affecting the “substantia nigra,” a small area of cells in the mid-brain. Degeneration of these cells as a result of free radical activity results in a reduction in levels of the neurotransmitter dopamine and upsets the balance between dopamine and another brain chemical, acetylcholine. The most familiar signs of the disease are tremor, or trembling in hands, arms, legs, jaw, and face; a generalized slowness of movement, stiff limbs, rigid facial expressions, and problems with balance or gait. Depression often precedes the physical signs, and mental function can deteriorate in advanced cases.

There’s no cure for Parkinson’s, but progression can be slowed and symptoms managed with a variety of drugs including L-Dopa (Levodopa) and Sinemet (Carbidopa). L-Dopa is converted to dopamine in the brain. Sinemet prevents L-Dopa from being broken down before it reaches the brain.

Glutathione is an antioxidant and free-radical scavenger found in the brain. In Parkinson’s disease, glutathione levels are reduced in dopamine neurons (brain cells containing dopamine). Some studies have shown that administering glutathione intravenously can help improve symptoms in Parkinson’s patients. Theoretically, glutathione limits the action of free radicals.

The physician who has directed the most research on this is David Perlmutter, M.D., a neurologist in Florida. I checked with him after receiving your question and learned that he has completed a double-blinded, placebo controlled study to be published later this year in a peer-reviewed medical journal. While he cannot discuss the clinical data prior to publication, Dr. Perlmutter indicated that his findings demonstrate glutathione administration was “quite effective” in treating the Parkinson’s patients who participated in the study.

In an interview in 2008, Dr. Perlmutter was quoted as saying that 80 to 90 percent of Parkinson’s patients treated with glutathione improve dramatically. He said that while glutathione doesn’t raise dopamine levels, it allows dopamine in the brain to become more effective. He also noted that glutathione can increase sensitivity to the neurotransmitter serotonin, which may explain why many of his depressed PD patients improve so markedly. Dr. Perlmutter reported that he has been treating Parkinson’s patients with glutathione for three years, administering it as a 10-minute, intravenous (IV) infusion three times a week. Dr. Perlmutter explained that glutathione must be given IV; given orally, it breaks down very rapidly. He said that in some cases, patients improved so dramatically that the dosage of the medications they take for the disease could be reduced. (Please read my response at the end on suppositories)

We’ll know more after Dr. Perlmutter’s study is published. I’ll update my Web site when the new information is available.

Andrew Weil, M.D.

Comment:

Dr. Perlmutter owns a pharmacy that he refers people to to purchase this very expensive and un necessary route of administration of Glutathione.  I’ve spoken on this much in many of my video’s and posts. Doing an IV usually a push or in some cases a slow infusion will keep peak plasma levels in your blood for an hour at best. Think of your cells taking the opportunity during that peak plasma to attempt to draw the glutathione into the cell where it is going to do good for you. For Parkinsons’ this is into the brain cells that are dopenergic or dopamine producing. Consider that a suppository will slow release over 5-7 hours which gives your brain and body the opportunity to absorb the Glutathione much better and also the application being every day and not just 3 days a week is also an advantage. Who wants to get an IV every day or even 3 days a week when there is a better, gentler, and more effective way? The proof is in the pudding you need just try suppositories to feel the difference if you’ve been on the IV.  GlutaMax is a powerful and highly potent product as it’s kept cold an shipped cold and has the highest content available at 500mg per suppository.

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Welcome to GlutGENIC.com

“Providing the highest Quality Glutathione Available”

Molecular structure of reduced glutathione used with all GlutaSource.info products

The GlutaGenic team would like to congratulation you on your commitment to take your health to the next level. As you explore the website, you are taking the first step towards transforming your level of energy. vitality, and health status. We are excited to share our ideas and effective products with you because they represent a monumental shift in healthcare delivery. 

Glutagenic utilizes high potency Glutathione via effective delivery methods such as nebulization, suppository, and endonasal routes. Click the buttons below to explore videos illustrating how Glutathione has made a difference in the health status of various individuals.


High Glutathione levels will help you to attain the physical, psychological, and physiological vibrancy that you desire and deserve. Most of you realize that your physical health is the most important thing that you possess. Utilizing the resources and products at GlutaGenic.com, you too can have the health, energy, and vitality you deserve.

Best wishes,

 

 

 

 

John Lieurance, D.C., N.D.

& the GlutaGenic Team

 

 

 

Glutathione and Parkinson’s disease is the elephant in the room & Roles of glutathione (GSH) in dopamine.

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Since it’s discovery Glutathione has been the focus of thousands of research investigations as it relates to a healthy brain and nervous system. Neuron Theory states the brain needs fuel and activation. Fuel in the form of oxygen and glucose and activation means it needs to be used or the nerves “fired” to keep them viable. This is the focus of the “new medicine” with Functional Neurology and the use of Glutathione Therapy. My personal experience treating Parkinson’s disease is such that the substatia Nigra which produces dopamine and regulates many motor and modalities must be treated with a balance of both fuel and activation. At the Parkinson’s Institute Sarasota

2008 Apr-May;62(4):236-49. Epub 2008 Mar 14.

Glutathione and Parkinson’s disease: is this the elephant in the room?

Source

Abstract

At least 2 decades have past since the demonstration of a 40-50% deficit in total glutathione (GSH) levels in the substantia nigra in patients with Parkinson’s disease (PD). The similar loss of GSH in the nigra in Incidental Lewy body disease, thought to be an early form of PD, indicates that this is one of the earliest derangements to occur in the pre-symptomatic stages of PD. Oxidative damage to lipids, protein and DNA in the nigra of PD patients is consistent with the loss of the antioxidant functions contributed by GSH. Past clinical trials that have used an antioxidant approach to treatment have used antioxidants that might substitute for GSH but these have shown modest to little benefit. More recent studies of the functions served by GSH in cells include in addition to its well-known participation in H(2)O(2) and toxin removal, such roles as modulation of protein function via thiolation which may control physiological and pathophysiological pathways to include DNA synthesis and repair, protein synthesis, amino acid transport, modulation of glutamate receptors and neurohormonal signaling. These multifunctional aspects to the workings of GSH in the cell would suggest that its loss perturbs many different processes and that replenishment and maintenance of GSH per se may be the best approach for preventing progressive damage from occurring. Despite this, few studies have been directed at specifically restoring GSH, although, as discussed herein, its unsanctioned use in PD is growing in popularity. This review will focus on glutathione in PD; the various functions carried out by glutathione and possible consequences of its depletion, as well as measures to elevate GSH in the CNS and its use in humans. Consideration of how the CNS generates and handles the substrates for GSH synthesis is also addressed with the view in mind that this may provide insights into control and maintenance of intracellular glutathione.

Roles of glutathione (GSH) in dopamine (DA) oxidation studied by improved tandem HPLC plus ESI-MS.

Abstract

In this study, new procedure with improved tandem HPLC plus ESI-MS was utilized to decipher the protective role of glutathione (GSH) against dopamine (DA) oxidation. We demonstrated that auto-oxidation of DA could produce aminochrome (AM, a cyclized DA quinone), which could be effectively abrogated by reductants, especially by GSH. Furthermore GSH was demonstrated to be able to conjugate with AM to form various conjugates via condensation reactions without enzymatic catalysis. The GSH-AM conjugates tend to aggregate, possibly mediated by conjugated AM structures, but could be inhibited by GSH. We hypothesized that proteins conjugated by AM might facilitate Lewy body formation of Parkinson’s disease (PD) in dopaminergic neurons via similar polymerization. We proposed that GSH could protect dopaminergic neurons against DA-induced toxicity via various mechanisms. The imbalance between DA oxidation and GSH protective capacity could be a key factor contributing to PD. Strategies to use GSH analogues, GSH inducers or to control DA oxidation might work to control PD onset and development.

Conclusion:

If you have Parkinson’s Disease you should take a serious look  at Glutathione Therapy! Keep in Mind that you can’t take Glutathione orally as it will not absorb throughout the gut so don’t waste your money on pills. Our products WILL absorb into the body and most importantly the brain. GlutaMax suppositories is out most popular product for PD sufferers.

Our Functional Neurology programs consist of various activation protocols that keep the brain and dopaminergic system firing using Functional Cranial Release or FCR. See FunctionalCranialRelease.com for more on this program and Parkinsons’. Make sure you sign up for the FREE “7 Secrets to Raising Glutathione” to learn how to naturally improve Glutathione as well.

Yours in Health,

John Lieurance, NMD, DC

Glutathione Suppositories are a very effective skin whitening if you will take it on a greater dosage.

Glutathione is a very good anti-oxidant, and a very effective whitening if you will take it on a greater dosage. Glutathione is an anti-oxidant that cleans the liver, takes off free-radicals and helps the brain too.  Our brain’s primary anti-oxidant is glutathione and that low level of it results to some illneses and disorders? The most advisable dosage is 10-20mg/kg BodyWeight to use glutathione  for whitening it has to be 20-40mg/kg/BW. example: 50kg x 20mg = 1000mg.  So for a 100 lb person you will need to take 2,000 mg a day. That is 4 GlutaMax suppositories a day. You should also take it with 1,000 mg vitamin c in ascorbic acid form to be able to maximize its whitening effect. For most people, the first 3 months use of gluta is crucial for it is the time where gluta is building the foundation (body chemistry re-alignment) and once built this is only the start for its whitening process. the lightening of skin is gradual (speed is depending on your metabolism and body chemical functioning) this is where you will notice that your skin is shinier and healthier than before. after this process, you will notice that your shade is lighter than before. For skin lightening, avoid products with HYDROQUINONE.

Other things to help
Licorice extract

magnesium ascorbyl phosphate

Lemon Juice

Rosehip Oil

 
Dr. John

Glutathione and Parkinson’s disease: Is this the elephant in the room?

Abstract

At least 2 decades have past since the demonstration of a 40–50% deficit in total glutathione (GSH) levels in the substantia nigra in patients with Parkinson’s disease (PD). The similar loss of GSH in the nigra in Incidental Lewy body disease, thought to be an early form of PD, indicates that this is one of the earliest derangements to occur in the pre-symptomatic stages of PD. Oxidative damage to lipids, protein and DNA in the nigra of PD patients is consistent with the loss of the antioxidant functions contributed by GSH. Past clinical trials that have used an antioxidant approach to treatment have used antioxidants that might substitute for GSH but these have shown modest to little benefit. More recent studies of the functions served by GSH in cells include in addition to its well-known participation in H2O2 and toxin removal, such roles as modulation of protein function via thiolation which may control physiological and pathophysiological pathways to include DNA synthesis and repair, protein synthesis, amino acid transport, modulation of glutamate receptors and neurohormonal signaling. These multifunctional aspects to the workings of GSH in the cell would suggest that its loss perturbs many different processes and that replenishment and maintenance of GSH per se may be the best approach for preventing progressive damage from occurring. Despite this, few studies have been directed at specifically restoring GSH, although, as discussed herein, its unsanctioned use in PD is growing in popularity. This review will focus on glutathione in PD; the various functions carried out by glutathione and possible consequences of its depletion, as well as measures to elevate GSH in the CNS and its use in humans. Consideration of how the CNS generates and handles the substrates for GSH synthesis is also addressed with the view in mind that this may provide insights into control and maintenance of intracellular glutathione.

Dr. Perlmutter owns a pharmacy that he refers people to to purchase this very expensive and un necessary route of administration of Glutathione.  I’ve spoken on this much in many of my video’s and posts. Doing an IV usually a push or in some cases a slow infusion will keep peak plasma levels in your blood for an hour at best. Think of your cells taking the opportunity during that peak plasma to attempt to draw the glutathione into the cell where it is going to do good for you. For Parkinsons’ this is into the brain cells that are dopenergic or dopamine producing. Consider that a suppository will slow release over 5-7 hours which gives your brain and body the opportunity to absorb the Glutathione much better and also the application being every day and not just 3 days a week is also an advantage. Who wants to get an IV every day or even 3 days a week when there is a better, gentler, and more effective way? The proof is in the pudding you need just try suppositories to feel the difference if you’ve been on the IV.  GlutaMax is a powerful and highly potent product as it’s kept cold an shipped cold and has the highest content available at 500mg per suppository.

John Lieurance, ND, DC

Why Does The American Medical Association Keep Rejecting The Approval Of Glutathione Therapy For Parkinson’s Patients?

Below is a spear campaign on Dr. Perlmutter. I agree with some of what is being said. We do need more research to explain why we are seeing benefit to our patients with Parkinson’s when we administer Glutathione. The fact that the AMA doesn’t endorse Glutathione as a therapy for PArkinson’s is not a reason to simply write off Glutathione as a valid treatment option. The AMA is famous for siding with big pharma. All of their publications are paid for by big advertising from drug companies and they are not always going to be pro a natural alternative which is natural and effective.  I agree that the IV method is a poor way to go with folks that need to be on a steady supply of Glutathione and that suppositories are much better. Please read the following with this in mind.
Yours in Health,
Dr. John Lieurance
…First let’s explain what “Glutathione” is and what it’s good for. Glutathione is a Tripetide and a Tripetide is a Peptide and a Peptide is a compound which is formed by linking one or more amino acids with a covalent bond.

YOU HAVE GOT TO BE KIDDING ME !, How can anyone without some type of medical degree even begin to understand all of this. Let’s try to explain this in a way that most people can understand, specifically people who might consider using Glutathione to treat their Parkinson’s Disease.

Glutathione is a system in the body of antioxidant’s that helps neutralize “out of control” oxygen in our bodies also known as “Free Radicals”. Out of control oxygen can speed up our ageing process, make our joints stiff, harden our blood vessels and promotes cancer.

Antioxidants are regulated by “The Glutathione System” within our bodies and coordinates how cells in our bodies “live” or “react” to threats such as “Free Radicals”.

Types of Antioxidants are Vitamin A, C, E,  Selenium & Zinc which can be found in various foods that we eat such as broccoli, tomatoes, organic onions, potatoes, beans, peas, leafy greens etc…

it has been claimed by A Dr. David Perlmutter, “a self proclaimed authority on Glutathione Therapy for treating Parkinson’s Disease”, that high, pure doses of Glutathione (Antioxidants) injected directly into the blood stream of a Parkinson’s Patient could kill enough “Free Radicals” or “out of control oxygen” to make a positive, substantial difference in the life of a person with Parkinson’s Disease. The only problem with Dr. Perlmutter’s claim is that the (AMA) American Medical Association has refused to approve Glutathione Therapy for the treatment of people with Parkinson’s. In fact Glutathione Therapy for Parkinson’s patients has been around for over twenty years and yet the AMA still has not approved it as a viable, measurable treatment for people with Parkinson’s.

One must ask themselves WHY ?, why has the AMA not approved Glutathione Therapy as a treatment for Parkinsons’s Disease. The answer is very simple, because it does not work. In Fact studies on Glutathione Therapy for Parkinson’s patients where a placebo was used in place of Glutathione showed that over 30% of the people reported feeling much better. This finding pointed out that Parkinson’s Patients are desperately reaching for hope wherever they can find it. In addition when using Glutathione in Glutathione Therapy for Parkinson (As Suggested By Dr. Perlmutter Himself)  the preservation of Glutathione is critical for it’s suggested “proper use”, and can’t be kept at room temperature for more than 6 hours without refrigeration, otherwise it loses it’s effectiveness prior to intravenously being administered. Interestingly enough Dr. Perlmutter will take peoples money for his treatment, but he takes no responsibility for initiating a protocol that ensures the proper facilitation of his “Magic Potion”.

The fact that Glutathione Therapy for Parkinsons’s has not been approved by the AMA is the reason doctors such as Dr. Perlmutter have been able to offer the treatment to people with Parkinson’s who are desperately looking for relief and a cure. Doctors such as these prey on the hopes of people with Parkinson’s and launch massive artificial, self promoted public relation campaigns about their treatments. These doctors don’t care about the truth, they are more interested in fabricating false news on the matter, specifically using the unsupervised Internet as it’s primary conduit.

You have to be your own judge, but I can tell you that you should educate yourself with your disease and make sure that any treatment you receive be responsibly monitored and administered by your doctor. Steer clear of Doctors who video tape your “before & after” progress for any treatment they recommend. First of all you don’t know if what they are giving you is even what they want you to use later on after you leave their office.
Comment:
Dr. Perlmutter owns a pharmacy that he refers people to to purchase this very expensive and un necessary route of administration of Glutathione.  I’ve spoken on this much in many of my video’s and posts. Doing an IV usually a push or in some cases a slow infusion will keep peak plasma levels in your blood for an hour at best. Think of your cells taking the opportunity during that peak plasma to attempt to draw the glutathione into the cell where it is going to do good for you. For Parkinsons’ this is into the brain cells that are dopenergic or dopamine producing. Consider that a suppository will slow release over 5-7 hours which gives your brain and body the opportunity to absorb the Glutathione much better and also the application being every day and not just 3 days a week is also an advantage. Who wants to get an IV every day or even 3 days a week when there is a better, gentler, and more effective way? The proof is in the pudding you need just try suppositories to feel the difference if you’ve been on the IV.  GlutaMax is a powerful and highly potent product as it’s kept cold an shipped cold and has the highest content available at 500mg per suppository.
John Lieurance, ND, DC

Cordyceps: Anti-Inflammatory and Anti-Aging Capacity Due to Influence on Glutathione Recycling.

Cordycepin: Anti-Inflammatory and Anti-Aging Capacity.

John Lieurance, D.C., N.M.D.

3/18/2013 – 11:18 — cordyceps

Recently two interesting research papers on medical propensities of Cordycepin, the most well known of the active ingredients of wild Ophiocordyceps sinensis and also cultivated O.sas well as Cordyceps militaris, were published. The first study presents results of ongoing research at Nottingham University (UK) under the leadership of Dr. Cornelia De Moor. It is entitled: “Inhibition of polyadenylation reduces inflammatory gene induction” and published in RNA. The other paper published in Experimental Gerontology by a mostly Korean team is entitled: “Cordycepin (3′-deoxyadenosine) attenuates age-related oxidative stress and ameliorates antioxidant capacity in rats” and its summary – see below -closes with: “These results suggest that cordycepin is effective for restoring antioxidant status and decreasing lipid peroxidation in aged rats. Aging leads to the gradual loss of pro-oxidant/antioxidant balance and increase oxidative stress. Cordycepin treatment decrease oxidative stress and increase antioxidant status Cordycepin treatment can ameliorate antioxidants during aging and it might attenuate the age-associated disorders”.

Now, I do not have the medical back ground to judge the content or the value of these research articles. However, the Nottingham study suggests that Cordycepin has anti-inflammatory capacity that is worth to be investigated further for potential drug development. The Korean study is packed with graphics that leave the impression that negative impact from aging on cellular level has been reduced substantially in rats that have been treated with Cordycepin.

Of course these studies do not address the medical value of natural Yartsa gunbu, the complex of the ghost moth larva taken over by caterpillar fungus – Ophiocordyceps sinensis. However, they clearly indicate that the attention that Yartsa gunbu as a medicinal fungus receives is not made out of thin air.

References with abstracts:
Kondrashov, A., Hedda A. Meijer, Adeline Barthet-Barateig, Hannah N. Parker, Asma Khurshid, Sarah Tessier, Marie Sicard, Alan J. Knox, Linhua Pang, and Cornelia H. De Moor 2012. Inhibition of polyadenylation reduces inflammatory gene induction. RNA 2012. 18: 2236-22502

ABSTRACT
Cordycepin (39 deoxyadenosine) has long been used in the study of in vitro assembled polyadenylation complexes, because it terminates the poly(A) tail and arrests the cleavage complex. It is derived from caterpillar fungi, which are highly prized in Chinese traditional medicine. Here we show that cordycepin specifically inhibits the induction of inflammatory mRNAs by cytokines in human airway smooth muscle cells without affecting the expression of control mRNAs. Cordycepin treatment results in shorter poly(A) tails, and a reduction in the efficiency of mRNA cleavage and transcription termination is observed, indicating that the effects of cordycepin on 39 processing in cells are similar to those described in in vitro reactions. For the CCL2 and CXCL1 mRNAs, the effects of cordycepin are post-transcriptional, with the mRNA disappearing during or immediately after nuclear export. In contrast, although the recruitment of RNA polymerase II to the IL8 promoter is also unaffected, the levels of nascent transcript are reduced, indicating a defect in transcription elongation. We show that a reporter construct with 39 sequences from a histone gene is unaffected by cordycepin, while CXCL1 sequences confer cordycepin sensitivity to the reporter, demonstrating that polyadenylation is indeed required for the effect of cordycepin on gene expression. In addition, treatment with another polyadenyation inhibitor and knockdown of poly(A) polymerase a also specifically reduced the induction of inflammatory mRNAs. These data demonstrate that there are differences in the 39 processing of inflammatory and housekeeping genes and identify polyadenylation as a novel target for anti-inflammatory drugs.

Thiyagarajan Ramesha, Sung-Kwang Yooa, Sung-Won Kima, Seock-Yeon Hwangb, Sang-Hyun Sohna, Il-Woung Kima, Si-Kwan Kima 2012. Cordycepin (3′-deoxyadenosine) attenuates age-related oxidative stress and ameliorates antioxidant capacity in rats. Experimental Gerontology Volume 47, Issue 12, December 2012, Pages 979–987

ABSTRACT:
Free radical-induced oxidative damage is considered to be the most important consequence of the aging process. The activities and capacities of antioxidant systems of cells decline with increased age, leading to the gradual loss of pro-oxidant/antioxidant balance and resulting in increased oxidative stress. Our investigation was focused on the effects of cordycepin (3′-deoxyadenosine) on lipid peroxidation and antioxidation in aged rats. Age-associated decline in the activities of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR), glutathione-S-transferase (GST), reduced glutathione (GSH), vitamin C and vitamin E, and elevated levels of malondialdehyde (MDA) were observed in the liver, kidneys, heart and lungs of aged rats, when compared to young rats. Furthermore, serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), urea, and creatinine were found to be significantly elevated in aged rats compared to young rats. Aged rats receiving cordycepin treatment shows increased activity of SOD, CAT, GPx, GR and GST, and elevated levels of GSH, and vitamins C and E such that the values of most of these parameters did not differ significantly from those found in young rats. In addition, the levels of MDA, AST, ALT, urea and creatinine became reduced upon administration of cordycepin to aged rats. These results suggest that cordycepin is effective for restoring antioxidant status and decreasing lipid peroxidation in aged rats. Aging leads to the gradual loss of pro-oxidant/antioxidant balance and increase oxidative stress. Cordycepin treatment decrease oxidative stress and increase antioxidant status Cordycepin treatment can ameliorate antioxidants during aging and it might attenuate the age-associated disorders.

Cordyceps is a great idea and it works to help recycle Glutathione. Besides having the purest Cordyceps on the planet GlutaGenic provides Glutathione Suppositories and Nebulized formulas for advanced Glutathione delivery to the brain and body.

Dr. John Explains how Glutathione can improve brain function and Metabolic Capacity.

Using Glutathione as a brain enhancing tool is a good idea as glutathione feeds the brain energy and quenches all stress in the brain at a cellular level so the brain can use all its reserves to work at being a brain instead of putting out “fires”. Watch this video and discover the metabolic capacity of the brain. Remember your brain needs 3 things to be healthy; Glucose, oxygen, and stimulation. The challenge many folks have is that they must stay with in their own metabolic capacity. In this video Dr. John explains this and how Glutathione can help raise the ceiling on brain function so you can do more stimulation and get more out of any brain based treatment or exercise program by using Glutathione.

How to Raise Glutathione Levels: Cocao and Glutathione

How to Raise Glutathione Levels

Glutathione is one of the most important pro-health and anti-aging chemicals in your body.  It is a powerful antioxidant and detoxifier. Glutathione protects your body against heavy metals such as lead and mercury.  In fact, in my link on Fish Safety, I discuss how some people have gene that yields lower levels of glutathione and, therefore, increased levels of methylmercury after ingestion of fish.

Remember also that mercury attacks your precious testosterone, so glutathione is one of your body’s natural testosterone protectors.  Glutathione is involved in dozens of other critical systems and even protects your body’s Vitamin C.  And we know Vitamin C provides critical collagen protection, including that in your skin.

So how do we raise glutathione levels naturally?

1. ALA. Alpha-lipoic Acid also has another huge benefit:  increase one of the body’s primary antioxidants, glutathione. [2]  Raising glutathione levels has remained elusive and alpha-lipoic is one of the few proven ways of doing it.

2. Maca. This Peruvian aphrodisiac was found to increase the all-important natural super-antioxidants SOD and glutathione. [3]

3. Avoid Alcohol.  Alcohol consumption decreases glutathione.  Why?  Because alcohol creates a toxin that glutathione must detoxify. [1]

4.  Whey.  Whey protein raises glutathione levels, at least in individuals with various illnesses such as HIV and cystic fibrosis. [4]  Some animal studies, though, indicate that this should be for the general populace as well. [5]  However, almost all store wheys that I have seen are loaded with dangerous excitotoxins and I document that here in my link called No Whey! However, there is an alternative, undenatured or biologically active whey, which I document in my link called Yes Whey if you want more information.

5. Exercise.  Exercise increases the important form of glutathione. [6]  However, it should be kept in mind that this is the body’s natural response to the increased oxidative load that exercise places upon it.

6. Glucose/Sugars/High Glycemic Foods. A number of in vitro study of human epithelial cells showed that increased glucose led to decreased glutathione levels. [7][9]

7. Resveratrol.  Resveratrol increased glutathione in lung epithelial cells that were “smoke depleted”. [8]  Good sources of resveratrol are red wine, peanuts and cocoa. nuts and cocoa.

8. Suppositories, Nebulization, and Nasal Spray’s: GlutaGenic.com offers the highest strength and most bioactive Glutathione products on the market.

 

 

REFERENCES:

1) Alcohol and Alcoholism, 21(1):81-84, “ALCOHOL ENHANCES VITAMIN C EXCRETION IN THE URINE”

2) Arzneimittel-Forschung, 1992, 42:829-831

3) Journal Plant Foods for Human Nutrition (Formerly Qualitas Plantarum), Jun 2007, 62(2), “The Influence of Maca ( Lepidium meyenii ) on Antioxidant Status, Lipid and Glucose Metabolism in Rat”

4) Eur J Clin Invest, 2001 Feb, 31(2):171-8, “Oral supplementation with whey proteins increases plasma glutathione levels of HIV-infected patients’

5) Toxicol Ind Health, May 2009, 25(4-5):325-328, “Whey proteins influence hepatic glutathione after CCl4 intoxication”

6) J Appl Physiol, 1993 Feb, 74(2): 788-92, “Blood glutathione status during exercise: effect of carbohydrate supplementation”

7) Journal of Molecular Endocrinology, 2004, 33:797-803, “High glucose decreases intracellular glutathione concentrations and upregulates inducible nitric oxide synthase gene expression in intestinal epithelial cells”

8) American Journal of Physiology, Lung Cellular and Molecular Physiology, 294(3):L478–88, “Resveratrol induces glutathione synthesis by activation of Nrf2 and protects against cigarette smoke-mediated oxidative stress in human lung epithelial cells”.

 

9) FEBS, 2 Jan 2 1998, 421(1):19-22 “High concentration of glucose causes impairment of the function of the glutathione redox cycle in human vascular smooth muscle cells”

Best Research I’ve seen for Glutathione – Parkinson’s connection!

Oxidative stress as a cause of nigral cell death in Parkinson’s disease and incidental lewy body disease.

  1. Dr. P. Jenner DSc1,*,
  2. D. T. Dexter PhD1,
  3. J. Sian BSc1,
  4. A. H. V. Schapira MD2,
  5. C. D. Marsden FRS3

Article first published online: 8 OCT 2004

DOI: 10.1002/ana.410320714

Abstract

We examine the evidence for free radical involvement and oxidative stress in the pathological process underlying Parkinson’s disease, from postmortem brain tissue. The concept of free radical involvement is supported by enhanced basal lipid peroxidation in substantia nigra in patients with Parkinson’s disease, demonstrated by increased levels of malondialdehyde and lipid hydroperoxides. The activity of many of the protective mechanisms against oxidative stress does not seem to be significantly altered in the nigra in Parkinson’s disease. Thus, activities of catalase and glutathione peroxidase are more or less unchanged, as are concentrations of vitamin C and vitamin E. The activity of mitochondrial superoxide dismutase and the levels of the antioxidant ion zinc are, however, increased, which may reflect oxidative stress in substantia nigra. Levels of reduced glutathione are decreased in nigra in Parkinson’s disease; this decrease does not occur in other brain areas or in other neurodegenerative illnesses affecting this brain region (i.e., multiple system atrophy, progressive supranuclear palsy). Altered glutathione metabolism may prevent inactivation of hydrogen peroxide and enhance formation of toxic hydroxyl radicals. In brain material from patients with incidental Lewy body disease (presymptomatic Parkinson’s disease), there is no evidence for alterations in iron metabolism and no significant change in mitochondrial complex I function. The levels of reduced glutathione in substantia nigra, however, are reduced to the same extent as in advanced Parkinson’s disease. These data suggest that changes in glutathione function are an early component of the pathological process of Parkinson’s disease. The data presented suggest (1) there is oxidative stress in the substantia nigra at the time of death in advanced Parkinson’s disease that manifests in terms of increased lipid peroxidation, superoxide dismutase activity, and zinc levels; (2) there is a major impairment of the glutathione pathway in Parkinson’s disease; and (3) alterations in reduced glutathione levels may occur very early in the illness.

 

Comment: So what can you do? Well my best advise would be to sign up for the “7 Secrets to Raising Glutathione.” Consider supplementing with Glutathione but be careful as you cannot absorb through the gut or oral means. We carry the highest dose available in suppositories and nebulization.

Glutathione,Hyper-Sympathetic State, The Adrenals & The pH Challenge.

Hyper-Sympathetic State

Your nervous system is divided into the sympathetic and the parasympathetic nervous system. Stess is associated with the sympathetic nervous system which holds your fight or flight response. Your parasympathetic nervous system holds your resting and digesting signals. Many of my patients who are stressed out present to my office with a dominance of the sympathetic nervous system.  Some Common Causes of stress include; emotional, mental, chemical/nutritional, electromagnetic, structural/postural.

The Adrenals

Your pair of adrenals are located just on top of your kidneys and they are responsible for the production of cortisol, adrenaline and other catocholamines responsible for reving and charging you up in a stress response. When this system is chronically put on alert it leads to what is called a hypersypathetic state.

Prolonged Increases of Cortisol & Adrenaline can paralize your immune system by decreasing: interleukin, natural killer cell activity, T-lymphocytes,and  secretory IgA. STudies have also shown chronic stress responses linked to Increases blood sugar with a decreases insulin sensitivity (see hyperinsulinemia in chapter 11), Increases bone loss, Increases blood fats (cholesterol, triglycrides), Increases fat accumulation (especially at waist), Increases fluid retention, Increases protein breakdown (thats loss of muscle).

Symptoms of being in a hypersypathetic state include; increased allergies, osteoporotic tendencies,  loss of lean mass, increased infections, blood sugar swings, high cholesterol, obesity, edema, and poor carbohydrate utilization.

Mental and Emotional stress is very common in our society with busy schedules and deadlines to meet. Most americans are working more hours. An interesting fact is that our productivity is staying about thew same is the last couple of years, however our overall unemployment is unchanged. This says that people are working harder to keep up with production. We are the hard working “Japan” of the 1980′s!

The pH Challenge

I include a saliva pH challenge as a part of my basic lab work up,  what we do is introduce a half cup of lemon into the mouth and the pH of the saliva is checked every minute for 5 minutes. I often see a rapid rise in the saliva pH, this is a comom sign that there is a dominance of the sympathetic nervous system.

When your brain becomes stressed from adrenal stress it leads to inflamed. You have to quench this inflammation! Guess what is the main substance that does this in your brain and even to a large part your entire body?……….. Glutathione! If you’ve never heard of Glutathione then it’s likely you will hear much more about it moving forward as it’s your bodies main antioxidant.  We will look at a few dietary considerations as well as the concept of oxidative stress, the silent killer. 

Yours in Health,

 

 

 

 

John Lieurance, DC, ND

Learn how to Avoid Brain Degeneration. Glutathione and brain inflammation.

In order to avoid brain degeneration you must avoid inflammation of the brain. Since the brain doesn’t have pain sensation like other area’s of your body inflammation of the brain shows up as brain fog, balance and coordination problems, and poor memory. Digestion is key to maintaining a healthy immune system for 2 key reasons. One when your digestion is poor then your gut is inflamed and when your gut is inflamed you are likely to have a poor barrier which protects the absorption of foods that are partially broken down and metabolized. These foods are a source of immune reaction and can cause autoimmune , arthritis, hypothyroid, fatigue and generally chronic inflammation in the body and brain. The second reason is the lamina propria sub-layer and the submucosa layer of the small intestine have nodules that are part of the lymphatic system. These nodules contain white blood cells that destroy germs. Another common sense reason that poor digestion will effect your immune system is that many nutrients that are key to a healthy immune system will simply not be absorbed like zinc & B vitamins. When your brain becomes inflamed you have to quench this inflammation! Guess what is the main substance that does this in your brain and even to a large part your entire body?……….. Glutathione! If you’ve never heard of Glutathione then it’s likely you will hear much more about it moving forward as it’s your bodies main antioxidant. In the following paragraphs we will look at a few dietary considerations as well as the concept of oxidative stress, the silent killer. Read carefully to keep your brain healthy!

Soy, Glutamate, and MSG

Well hidden in so many processed foods, glutamate in the form of monosodium glutamate (MSG), soy protein extract, protein isolate, hydrolyzed vegetable proteins, natual flavoring or any of the other disguised names for MSG. Its so difficult to avoid as most fast-food chains and restaurants use at least one of these forms of glutamate to enhance the taste of there food.  These substances are toxic to your brain due to an excitatory and inflammatory action they have on the neuron. They call it an excitotoxin were it literally excites the cell to the point of self destruction.

Effects of MSG on Aging and Brain Inflammation.

In 1969, Dr. Olney noticed brain destruction of test animals in the area of the hypothalamus called the arcuate nucleus. The arcuate nucleous releases a substance that is necessary for the pituitary to release growth hormone. The pituitary gland, under normal conditions, secretes growth hormone in cycles. There is usually release that occurs when we fall asleep or take a nap!  This is an excellent reason for us to take a nap during the day (see restorative pose, Chap. 14), also children are benefited greatly due to the large demand of growth hormone. I have seen recent news stories where schools have stopped providing nap time due to striving to increase education. This is a big mistake, in my opinion. In regards to the above study on MSG and its effect of growth hormone release they found animals fed MSG not only produced less growth hormone, they also lacked the normal release cycles seen in all other mammals, including humans.6

Studies using immature mice have shown decreases in LH, FSH and prolactin  which are sex and reproductive hormones, growth hormone, adrenal regulating hormone, and thyroid regulating hormone following exposure to MSG. Deficiencies  in these hormones showed up in the animals as obesity, smaller growth, inability to reproductive, and slow metabolism. 9-13

Confirmation from more studies demonstrating males with atrophy of the testes and low levels of testosterone. Females where seen with low LH, FSH and estradiol-17beta which is the main form of estrogen hormone. In There was a 68% drop after MSG was given. 10

The young girls who begin developing breasts, and beginning menses, earlier than normal may be due to glutamate consumption. Since soy contains phytoestrogens and high glutamate levels consuming soy can be a leading factor for this anomaly.13

Studies found that infant animals given  MSG have high cortisol levels than normal mice, and after stressful events it would take longer for the high levels to come down to normal levels.14

There is an area in the brain called the hippocampus and it is where your memerory centers are located. Its though that high cortisol can cause damage to these neurons through up regulating oxidation in this area. Damage and degeneration of the hippocampus results in the condition known as Alzheimer’s disease. Its though by some that having cortisol levels elevated chronically  from childhood can be quite impactful in ones ability to enjoy memory. The clearence factor is the ability to unwind and I’ve found that treating the high cortisol levels make a big impact on the ability to relax after a tuff day as well as not get so worked up over small events that would otherwise get them excited, elevating their cortisol. Studies have shown that there is a low glutathione saturation in the hippocampus which leads to this damage and inflammation.

Oxidative Stress, Rust

When metal rusts, it’s a sign of the chemical process known as oxidation. Rusting indicates the damage incurred by exposure to oxygen; we say the metal is becoming oxidized. Its when oxygen steals electron from the metal that it distroys the metal changing the physical and chemical properties. Oxidation also takes place when you bite into an apple if left out it will  turn brown as it’s exposed to oxygen in the atmosphere. The process of oxidation causes molecules with uncoupled electrons. These are called free radicals and they are linked to DNA damage which creates cancer cells, aging of organs and skin, arthritis and too many other degenerative diseases to name.

We all need oxidants in our body. However too much oxidant molecules can cause injury to our body.  Oxidative stress is the technical name for this process. This phenomenon was first noted in 1954 by Dr. Denham Harmon, an organic chemist at the University of California, Berkeley. Dr. Harmon theorized that oxidants were the cause of aging, as well as the major cause of most diseases. His theory has continued to hold up and has received substantial verification over the past half century. 

Most of the conditions that we associate with aging, such as wrinkles, heart disease, and Alzheimer’s, are related to excess oxidative stress in the body. As Dr. Harmon stated, “Very few individuals, if any, reach their potential maximum life span; they die instead prematurely of a wide variety of diseases—the vast majority being ‘free radical’ diseases.” Although Dr. Harmon’s research is a half-century old, in the last five years alone, more than five thousand articles on the subject have appeared in research journals. Until recently, tests to measure levels of oxidative stress were expensive and only available to research centers. Today there is, an extremely acurate, over-the-counter urine test available called an oxidata test. Information is available at www.oxidata.com.

ORDER A 4 MONTH OXIDATA TEST KIT

Sources of oxidative stress can be both internal and external. The external ones include exposure to any kind of environmental pollution, petrochemicals, or heavy metals. There are also lifestyle-related causes of oxidative stress, such as smoking, drinking alcohol, caffinated beverages like coffee and tea, excessive exercise, prescription drug-and especially overeating. Trying too hard to get a tan can also hurt too much sun (ultraviolet radiation) contributes to oxidative stress.

Internal sources of oxidative stress include infections  (both  acute and/or chronic), blood sugar imbalance lead to increased free radicals,  high levels of adrenaline and  high levels cortisol.

Reduction / Dampness

When your body is subjected to chronic oxidation over a period of time the body can become saturated with electrons. This congests a part of your cell called the mitochondria, its the part of your cell that generates all your energy. When this saturation occurs it’s called reduction. In Chinese medicine they call this dampness. Classically these people will be fatigued usually with a feeling of heaviness. Often the tongue is swollen, observed with tooth marks on the sides of the tongue.  This would not be a good time to take high amounts of anti-oxidants. This represents a good example of why nutrition programs should be closely monitored by a competent clinician with the ability to check these levels for you. Many times this shows up with a low oxidata score with abnormal adrenal states.

Vitamine C with very high bioflavinoids

Recent studies have demonstrated that flavinoids are powerful antioxidants, acting against a whole host of dangerous free radicals. In fact, some of the flavonoids can neutralize special free radicals that cannot be neutralized by antioxidant vitamins. It should be noted that there are other dangerous radicals besides oxygen radicals. Many people are unaware of  a reactive nitrogen species that can be equally, if not more, destructive than oxygen radicals (free radicals). Vitamins are poor at neutralizing these special types of radicals, while flavonoids are very efficient. I regularly test for nitate levels inpateints and bioflavinoids will greatly help normalize these levels. Many times the liver is doing a poor job and neutralizing these compounds usually due to being overburdened with toxicity Its common for these high nitrate levels to cause swelling and congestion of the sinuses. Many of the chronic sniffls, runny noses and post nasal drips are a result of excessive nitrat levels.

Flavonoids can remove (chelate) dangerous metals, such as, copper, aluminum, mercury, arsenic and lead.   Iron and aluminum accumulation is commonly associated with degenerative disorders of the nervous system such as Alzheimer’s and Parkinson’s disease.

Its the flavonoids and carotenoids that allow plants to survive in the glaring sun all day long. Without flavinoids the sun’s harsh rays would quickly destroy the leaves. Flavonoids absorb the harmful radiation from the sun by neutralizing the free radicals they generate. This is similar to how flavinoids work for us!

Recent years has yelded massive research into the medicinal properties of flavonoids. They seem to be finding they not only protect us from antioxidants, they also help in the treatment and prevention of many cancers.

Oxidata Urine testing

This tests for an end product of polyunsaturated fat chain where malondialdehydes form as a result of free radical attack. I include an oxidata urine test with my stadard lab work up on each of my pateints.3-10

Yours In Healhty,

 

John Lieurance, DC, ND 

 

 

References

1. Dhanakoti S.N., “Response of Urinary Malondialdehyde to Factors that Stimulate Lipid Peroxidation in

Vivo.” Lipids 22(9):643-6, Sept 1987.

2. Draper H.H., “Malondialdehyde Derivatives in Urine.” Basic Life Sci. 49:199-202, 1988.

3. Draper H.H., “Urinary Malondialdehyde as an Indicator of Lipid Peroxidation in the Diet and in the Tis
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4. Hubbard R., lacono R., Westengard J., and Schoonberg T., “Malondialdehyde (MDA) Studies in Palli-
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5. Hubbard R., lacono R., Westengard J., and Schoonberg T., “Urine Malondialdehyd (MDA) Measured in
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6. Lin JY, Pan JT. Single-unit activity of dorsomedial arcuate neurons and diurnal changes of tuberoinfundibular dopaminergic neuron activity in female rats with neonatal monosodium glutamate treatment. Brain Research Bulletin 48(1999): 103-108. Mailer D, Underwood LE, et al. Neonatal treatment with monosodium glutamate:effects of prolonged growth hormone (GH)- releasing hormone deficiency on pulsatile GH secretion and growth in female rats. Endocrinology 128(1991): 1100-1106.

7. www.Oxidata.com / urinary oxidative stress test.

8. www.pzizz.com  / Nap machine.

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14. Skuletyova I, Kiss A, Jezova D. Neurotoxic lesions induced by monosodium glutamate result in increased adrenopituitary proopiomelanocortin gene expression and decreased corticosterone clearance in rats. Neuroendocrinology 67(1998): 412-420.

 

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