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Lou Gehrig’s Disease Linked to Low Glutathione Levels

August 1st, 2009

Although treatment for ALS, Lou Gehrig’s disease has still eluded those in the medical profession, scientists have discovered mechanisms that are underlying the disease process that are considered to be useful in the clinical management of ALS, giving new hope for significantly slowing the disease process and improving the quality of life for these patients.

 

The following article published in PubMed makes it very clear as to the possible benefits that increasing glutathione will have on slowing the progression of the disease. Although, this is not a “cure” it is certainly a step in the right direction in treating a disease that up until now has only one outcome.

A study of glutathione S-transferase pi expression in central nervous system of subjects with amyotrophic lateral sclerosis using RNA extraction from formalin-fixed, paraffin-embedded material.

Usarek E, Gajewska B, Ka?mierczak B, Ku?ma M, Dziewulska D, Bara?czyk-Ku?ma A.

Department of Biochemistry, Medical University of Warsaw, Banacha 1, 02-097, Warsaw, Poland.

The expression of glutathione S-transferase pi (GST pi), an enzyme responsible for inactivation of a large variety of toxic compounds was studied in spinal cord, motor and sensory brain cortex obtained from patients who died in the course of amyotrophic lateral sclerosis (ALS). The studies were performed on formalin-fixed, paraffin-embedded (FFPE) and freshly frozen tissues. The method of RNA isolation from FFPE was modified. A significant decrease of GST pi-mRNA expression was found in cervical spinal cord and motor brain cortex of ALS subjects comparing to analogue control tissues (P<0.01), as well as in motor cortex of ALS subjects comparing to their sensory cortex (P<0.05). In spinal cords the decrease in GST pi-mRNA expression was accompanied by a decrease of GST pi protein level. Results indicated lowered GST pi expression on both mRNA and protein levels in the regions of nervous system affected by ALS. The non-properly inactivated by GST toxic electrophiles and organic peroxides may thus contribute to motor neurons damage.

 

What is Glutathione?

Glutathione’s role is to protect us against the main villains (toxins) that are at the root of aging and the multitude of diseases that are commonplace in society today. Glutathione in essence is the body’s Master Antioxidant! Yes, we have our own detoxification system built right in from birth.

Glutathione is rapidly consumed on a daily basis through normal metabolism, exercise and illnesses. We regenerate glutathione repeatedly but unfortunately more is lost than is manufactured by the body. We lose approximately 8 -12% of glutathione levels per decade from age 20 on. It is no wonder that the aging process seems to hit so many by their 40’s.

Without your glutathione levels at a optimum level, you have less than adequate defenses against may illnesses and diseases, including diabetes, heart disease, hypertension, lupus, Lou Gehrig’s disease and the list goes on.

How to Raise Your Glutathione Levels

Glutathione is made by the cells in our bodies from 3 amino acids: glycine, glutamate and cysteine.  Cysteine is the most important part of this equation and the most difficult to get. 

Research Scientist, Dr. Robert Keller, MD, MS, FACP, AAHIVS, the Director of Medicine and Research/KBK at the Institute of Advanced Medicine, has spent years on developing a way to help the body to produce glutathione to increase the quality of life for many of his patients. His research has lead to the revolutionary product that is a formulation of natural ingredients that is proven to increase the levels of glutathione in the body by 400%.

With Dr. Keller’s research and the many positive results that he has seen in the quality of life for his patients, he could see the potential for everyone taking this product to have a better quality of life, regardless of illness or age.

To find out more about Dr. Keller’s revolutionary product go to: MaxGXL Glutathione Accelerator

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Amy McFarland Uncategorized

Medical Conditions Associated With Low Glutathione Levels

August 1st, 2009

Medical Conditions Associated With Low Glutathione Levels

Glutathione’s potential importance is being noted in a variety of diseases that are now being associated with decreased glutathione levels. For example, aging, Alzheimer’s and acne and in the most recent health scares, the Bird Flu and MRSA.

Consequences of Decreased Glutathione[i]

General:

Obesity, immune signaling, endothelial dysfunction, alcoholism, inflammation, heavy metal poisoning

Cardiovascular:

Angina and spastic angina, unstable angina, heart attacks, positive stress tests, reperfusion after cardiac bypass surgery

Pulmonary:

Emphysema (COPD), pulminary fibrosis (IPF), asthma, muscle wasting in COPD, chronic bronchitis, tobacco use

Neuro/Psych:

Migrane headaches, Alzheimer’s, Arkinson’s, multi infarct dementia, autism, ADHD (attention deficit hyperactivity disorder), bipolar disease, schizophrenia, Lou Gehrig’s disease, Huntington’s chorea, multiple sclerosis (MS), depression

Opthamology:

Cataracts, macular degeneration

Infectious Disease/Immunology:

Hepatitis a, b, and c; herpes simplex; herpes zoster/shingles; influenza and bird flu; HIV;  MRSA; common viral infections (upper respiratory, gastroenteritis); others

Rheumatology:

systemic lupus erythematosus (SLE);  rheumatoid arthritis (RA);  mulitiple sclerosis (MS);  systemic sclerosis (scleroderma) syndrome;  Behcet’s syndrome; ME/CFS; fibromyalgia; others

Dermatology:

Wrinkles, sagging; acne; psoriasis; atopic dermatitis;  exema; others

Oncology every cancer studied including:

brain; head and neck; thyroid; lung; esophagus; stomach; intestine; liver; pancreas; kidney; uterine; ovarian; prostrate; leukemia (acute and chronic); lymphoma; multiple myeloma; others

OB/GYN:

Infertility; spontaneous abortions; pre menstrual syndrome

Since there are few rigorous scientific studies demonstrating that increasing glutathione levels will improve the outcome of any disease or clinical condition, these statements have yet to meet the science demands of the cause and effect relationship.

It is just now coming into light that increasing glutathione levels has dramatically increased the quality of life for so many who are afflicted with these various diseases.

[i] “Glutathione-Your Best Defense Against Aging, Cellular Damage and Disease” by Dr. Robert H. Keller MD, MS, FACP, AAHIVS, Director of Medicine & Research/KBK Institute of Advanced Medicine

 

DISCLAIMER


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Amy McFarland Autism and Glutathione, Decreased Glutathione Levels, Heart Disease and Glutathione, MaxGXL Glutathione Accelerator, Menopause and MaxGXL, Parkinson's and Glutathione, Uncategorized

Menopause and MaxGXL

July 27th, 2009

Suffering from the symptoms of menopause or starting perimenopause?

 

Here is an interesting article from Pubmed about the favorable effects of dietary antioxidants nutraceuticals (specifically Glutathione, superoxide dismutase, vitamin C & E)

 

MaxGXL & Max N-Fuze Are Teaming Up for Menopause Symptom Reduction

 

Menopause: a review on the role of oxygen stress and favorable effects of dietary antioxidants.

 

Department of Biotechnology, University of Alicante, San Vicente, Alicante, Spain.

Menopause is often accompanied by hot flashes and degenerative processes such as arteriosclerosis and atrophic changes of the skin that suggest an acceleration of aging triggered by estrogen lack. Therefore, hormone replacement therapy (HRT) has been considered the most suitable treatment for the above symptoms and processes. However, because of the possible

serious side effects of HRT (especially the increased risk of thrombo-embolic accidents and breast cancer) there is a growing demand for alternative treatments of the symptoms and pathological processes associated with menopause. In agreement with the above, we review research that supports the concept that oxygen stress contributes to menopause and that some of its physiopathological effects may be prevented and/or treated improving the antioxidant defense of menopausic and postmenopausic women. Accordingly, a selection of micronutrients may be useful as a dietary supplement for protection against the decline of physiological functions caused by age-related oxygen stress. Since aging is accompanied by a progressive oxidation of the physiological sulfur pool, we emphasize the role of the vitamins B that help to maintain the GSH/GSSG ratio in its normal reduced state. Nutritional supplements should also include the key antioxidant vitamins C and E, as well as beta-carotene and the mineral micronutrients found in the oxygen radical-detoxifying enzymes glutathione peroxidase and superoxide dismutase.

 

Moreover, the reviewed data support the concept that other antioxidants such as lipoic acid and the precursors of glutathione thioproline (TP) and l-2-oxothiazolidine-4-carboxylic acid (OTC), as well as the soy isoflavones and the “coantioxidants” of an hydroalcoholic extract of Curcuma longa may help to prevent antioxidant deficiency with resulting protection of mitochondria

against premature oxidative damage with loss of ATP synthesis and especialized cellular functions. Therefore, the administration under medical advice of synergistic combinations of some of the above mentioned antioxidants in the diet as well as topically (for skin protection) may have favorable effects on the health and quality of life of women, especially of those who cannot be treated with HR, suffer high levels of oxygen stress, and do not consume a healthy diet that includes five daily rations of fresh fruit and vegetables.

 

Max N-Fuze is a prime example of tomorrow’s nutrition, today.

 

It exemplifies the best in bioavailability of key nutrients via unique nanotechnology. Max NFuze supplies a proprietary blend that works in concert with MaxGXL to support cellular defenses. Furthermore, Max N-Fuze provides 19 targeted vitamins and minerals needed for cellular health. Max N-Fuze supplies the power of many products into one convenient single serve pouch.

 

Good health is not a random equation.

 

The body relies on a specific roster of nutritional teammates in order to function, protect and communicate properly. For instance, the synthesis of coenzyme Q10 involves a complex process requiring at least eight vitamins along with several trace elements and amino acids. A deficiency in any of the required amino acids, vitamins and minerals impairs the formation of  oenzyme

Q10 in the body.

 

Another example is glutathione. Glutathione needs vitamin C, lipoic acid, selenium, zinc and riboflavin. The list of cooperation between nutrients goes on and on. For this reason, the nutrients provided in Max N-Fuze are not in the formula simply because of some arbitrary standard. Rather, Max N-Fuze supplies specific targeted nutrients for the purpose of supporting optimal cellular defense, communication and function as the body goes about its miraculous tasks.

 

Your Body Doesn’t Leave Things Up to Chance

 

Dr. Robert H. Keller calls MaxGXL and Max N-Fuze the “Dynamic Duo” for good reason. The human body houses a fascinating network of cooperating antioxidants. There is a team of antioxidants that is so important that it was not left to chance. This irreplaceable team of antioxidants is made by the body, for the body. The All-Star captain of this antioxidant team is glutathione. However, glutathione doesn’t work alone.

 

In Dr. Keller’s scientific monograph, Glutathione: Your Best Defense Against Aging, Cellular Damage and Disease, he explains that the body has four main endogenous (created in the body) antioxidants:

 

• Glutathione (GSH)

• Superoxide dismutase (SOD)

• Catalase (CAT)

• Coenzyme Q10 (CoQ10)

 

You might call these powerful antioxidants the “Fab Four” because they single handedly go up against a coalition of utterly devastating free radicals that includes:

 

Superoxide, alkoxyl peroxide, hydroxyl, nitric oxide, hydroperoxyl, singlet oxygen, hypochlorous acid (better known as bleach) and hydrogen peroxide.

 

MaxGXL and Max N-Fuze are the “Dynamic Duo” because while MaxGXL increases glutathione, Max N-Fuze is formulated to support superoxide dismutase, catalase, and CoQ10. Together, these two products offer you the best in full-spectrum cellular defense and unparalleled delivery of 19 high performance vitamins and minerals.

 

It is clear that people are experiencing the difference, and living the benefits of this dynamic duo, and the word is getting out.

 

Consider MaxGXL and Max N-Fuze in your treatment of menopausal symptoms.

DISCLAIMER

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Amy McFarland Antioxidants and Free Radicals, Consumer Lab, Max International, MaxGXL Glutathione Accelerator, MaxGXL Patent, Menopause and MaxGXL, Uncategorized

MaxGXL™ Passes ConsumerLab.com’s Athletic Banned Substance Screening Program

July 27th, 2009

Salt Lake City, UT – July 19, 2007Max International is excited to announce that MaxGXL™ has passed ConsumerLab.com’s Athletic Banned Substance Screening Program. This program screens for over 170 substances (including metabolites) based on the 2007 World Anti-Doping Agency (WADA) Prohibited List. The screening included testing for Beta-Blockers, Diuretics, Narcotics, Anabolic Steroids, Stimulants, Masking Agents and Caffeine. To view MaxGXL™ on ConsumerLab.com’s website please click here.

 “The results of the screening demonstrate not only Max International’s commitment to quality and safety, but also our firm belief in seeking out independent bodies to research, test and validate our products,” said Max International President Craig Case. “MaxGXL™ is science and nature at its finest, and these results will only help to make the public aware of this wonderful product.”

MaxGXL™ is a compositionally patented nutritional product developed by renowned immunologist Dr. Robert Keller. It provides the necessary components of glutathione (GSH) that, when absorbed into the body, stimulate the body’s own production of glutathione to be used by every cell. Glutathione is the most prevalent, natural, powerful and multifunctional antioxidant in the human body and is employed by every organ.

 About Max International – Max International is a research and science based company that focuses on a proper blend of science and nature, founded in February 2007, and headquartered in Salt Lake City, Utah. For more information on MaxGXL™ and Max International visit www.maxgxl.com.

DISCLAIMER

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Amy McFarland Consumer Lab, Max International, MaxGXL Glutathione Accelerator, Uncategorized

Low Glutathione Levels Linked to Heart Disease

July 25th, 2009

Glutathione Deficiency in Cardiac Patients Is Related to the Functional Status and Structural Cardiac Abnormalities

Thibaud Damy,#1,2,3 Matthias Kirsch,#1,3 Lara Khouzami,2,3 Philippe Caramelle,2,3 Philippe Le Corvoisier,2,3,4,5 Françoise Roudot-Thoraval,3,6 Jean-Luc Dubois-Randé,1,2,3 Luc Hittinger,1,2,3 Catherine Pavoine,2,3 and Françoise Pecker1,2,3*
1AP-HP, Groupe hospitalier Henri-Mondor Albert-Chenevier, Fédération de Cardiologie, Département de Chirurgie Cardiaque, Créteil, France
2INSERM, U955, Créteil, France
3Université Paris12, Faculté de Médecine, UMR-S955, Créteil, France
4INSERM, Centre d’Investigation Clinique 006, Créteil, France
5Platform of biological resources, Groupe hospitalier Henri-Mondor Albert-Chenevier, Créteil, France
6AP-HP, Groupe hospitalier Henri-Mondor Albert-Chenevier, Département de Recherche Clinique- Santé Publique, Créteil, France
Alicia J. Kowaltowski, Editor
Instituto de Química, Universidade de São Paulo, Brazil
#Contributed equally.
* E-mail:francoise.pecker@inserm.fr
Conceived and designed the experiments: TD MK LK PLC JLDR LH CP FP. Performed the experiments: TD MK LK PC PLC FP. Analyzed the data: TD MK LK PC PLC FRT LH CP FP. Contributed reagents/materials/analysis tools: TD MK PLC JLDR FP. Wrote the paper: TD MK LK FRT LH CP FP.
Received December 2, 2008; Accepted February 2, 2009.

ABSTRACT

Background

The tripeptide glutathione (L-gamma-glutamyl-cysteinyl-glycine) is essential to cell survival, and deficiency in cardiac and systemic glutathione relates to heart failure progression and cardiac remodelling in animal models. Accordingly, we investigated cardiac and blood glutathione levels in patients of different functional classes and with different structural heart diseases.

Methods

Glutathione was measured using standard enzymatic recycling method in venous blood samples obtained from 91 individuals, including 15 healthy volunteers and 76 patients of New York Heart Association (NYHA) functional class I to IV, undergoing cardiac surgery for coronary artery disease, aortic stenosis or terminal cardiomyopathy. Glutathione was also quantified in right atrial appendages obtained at the time of surgery.

Results

In atrial tissue, glutathione was severely depleted (?58%) in NYHA class IV patients compared to NYHA class I patients (P=0.002). In patients with coronary artery disease, this depletion was related to the severity of left ventricular dysfunction (P=0.006). Compared to healthy controls, blood glutathione was decreased by 21% in NYHA class I patients with structural cardiac disease (P<0.01), and by 40% in symptomatic patients of NYHA class II to IV (P<0.0001). According to the functional NYHA class, significant depletion in blood glutathione occurred before detectable elevation in blood sTNFR1, a marker of symptomatic heart failure severity, as shown by the exponential relationship between these two parameters in the whole cohort of patients (r=0.88).

Conclusions

This study provides evidence that cardiac and systemic glutathione deficiency is related to the functional status and structural cardiac abnormalities of patients with cardiac diseases. These data also suggest that blood glutathione test may be an interesting new biomarker to detect asymptomatic patients with structural cardiac abnormalities.
To Read the complete Journal entry go to PubMed
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Amy McFarland Consumer Lab, Decreased Glutathione Levels, Heart Disease and Glutathione, Max International, MaxGXL Glutathione Accelerator, Uncategorized