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Montiff ATP
Adenosine Triphosphate

Montiff ATP Adenosine Triphosphate enhances energy and Krebs cycle functioning.

This product has MAJOR applications for a host of health concerns.

Montiff ATP Adenosine Triphosphate supports energy and Krebs cycle functioning.

Montiff ATP Adenosine Triphosphate DIRECTIONS

Take 1-3 tablets up to three times a day or as directed by a health care professional.

Each enteric coated tablet contains: 25mg of pure ATP produced from biological fermentation

Caution: ATP is safe substance, however, it is not recommended for those with hypotension, due to possible hypotensive effects.


What is Montiff ATP
Adenosine Triphosphate?

Montiff ATP Adenosine Triphosphate is a molecule found in the mitochondria, and is the energy source of all cells.

As part of the Krebs cycle, it is involved in the metabolic process of amino acid and carbohydrate metabolism. It is converted to ADP (Adenosine Diphosphate) which is the energy necessary for transmitting nerve cells, muscle contractions, and cell division. Co-Q 10, alpha lipoic acid, and phosphocreatine all have an effect on the production of ATP.

ATP is RECOMMENDED TO ENHANCE STRUCTURE & FUNCTION RELATING TO NUTRITIONAL DEFICIENCIES PERTAINING TO:

Cellular energy production necessary for healthy heart and brain function as well as energy for all living cells.
 **Has been used for patients with angina pectoris, and other coronary problems.**

To increase muscular contractions, which is useful for athletes resulting in longer and more vigorous workouts. 
Helps resolve impaired muscle function problems.

Hepatic and Liver function
. Detoxification of toxic compounds is vital to prevent liver cell death i.e. glutathione reduced, vitamin c, amino acid blend, b-vitamins, alpha lipoic acid, l-carnitine, and anti-oxidant blends.


Montiff ATP Adenosine
Triphosphate Benefits

Montiff’s ATP Adenosine Triphosphate  is the highest quality available. It is natural and made by biological fermentation.

President Don Tyson was the first person to introduce the active enteric preparation of ATP in 1984 to the United States. The tablets are enterically coated to allow them to dissolve in the small intestine for optimal absorption and assimilation.

ATP AND HEART FUNCTION

The heart muscle contains over 2 million myocytes, or heart cells that produce the energy necessary to contract, or beat, the normal 60 times a minute. ATP is the energy source of all heart cells. It may be indicated in conditions such as excess ammonia levels, angina pectoris, heart insufficiency, auricular fibrillation failures, coronary insufficiency, and myocarditis.

ATP AND ATHLETES

Increased ATP may enable more muscle contractions resulting in longer and more vigorous workouts. This can enhance sports activity and performance. ATP is recommended along with MONTIFF’S SUPER SPORTS amino acid formula for optimum results.

ATP AND ALCOHOL ABUSE

ATP levels decrease in alcohol abuse. Toxic compounds reactive oxygen species, aldehydic lipid peroxides, hydroxyl ethyl radicals, and acetaldehyde, cause cell death.

ATP AND AMINO ACID METABOLISM

ATP is involved in the Krebs cycle or citric acid cycle and is necessary for the proper metabolism of amino acids.

Low ATP interferes with the necessary biosynthesis required for proper Amino Acid metabolism and can also result in biochemical imbalances. These imbalances can create metabolic problems and effect proper neurotransmitter function. This may also effect the urea cycle and create harmful excess ammonia levels.

ATP is the primary source of energy for muscle contractions. Muscle contractions place a demand on ATP, resulting in insufficient amounts necessary for protein synthesis.

ATP AND BRAIN FUNCTION

ATP is necessary for the energy required for proper brain and nerve cells, and beneficial results have been noted with neurological problems, including cerebral arterial sclerosis and cerebral epilepsy.

ATP FOR THOSE WITH HEPATIC, LIVER & CEREBRAL HEMORRHAGE, ISCHEMIA & SHOCK. 
A rapid fall of tissue content of ATP has been noted in ischemic kidney tissue, and patients with hepatic, liver and cerebral hemorrhage, ischemia, and shock were administered ATP by IV infusion showed marked improvement in several studies. Therefore, it may be beneficial to follow-up with oral ATP supplementation.

ADDITIONAL POSSIBLE INDICATIONS INCLUDE:

SKIN: Atopic dermatitis and acute chronic eczema

MUSCULAR CONDITIONS: Progressive muscular atrophy, myasthenia, and progressive neuralgic amyotrophy.


EAR: Tinnitus, neurogenic difficulty in hearing, Meniere’s Syndrome.


EYE: Opthalmacopia.


SURGERY: Studies indicate positive results improving venous flap survival as well in by-pass surgical patients with ischemic heart diseases.


OTHER: Haemolytic anemia, gastroptosis, acute hepatitis, and acute nephritis.



REFERENCES:

Packer, Lester, PhD., Colman, Carol, The Antioxidant Miracle, 1999.


“The Effect of Glutathione, Superoxide Dismutase and Adenosine Triposphate on Venus Flap Survival”, European Journal of Plastic Surgery (Germany) 1996.


“The Effect of ATP on Heart Function of Patients with Chronic Ischemic Heart Disease After Aortacoronary Bypass Surgery”, Anesteziol Reanimatol (Russian Federation), 1993.


Champs, PC, Harvey, RA, Lippincott’s Ilustrated Reviews: Biochemistry. 1987.
“Evidence for Enhanced Uptake of ATP by Liver and Kidney in Hemorrhagic Shock”, Am. J. Physiol., 1977.


Rankin,AC et al., “Adenosine or ATP for Supraventricular Tachycardias? Comp. Dbl. Blnd.Study..”, American HeartJ.,1990


“Purine Metabolism in Ischaemic Kidney Tissue”, Danish Med. Bull., 1982.
Chaudry IH, Yale J. of Biol. Medicine, 1982.
Moro, C et al,

“Dose Related Efficacy of Aden. Triphosphate. In Spontan. Supraventricular Tach.”, Internat. J. of Cardiol., 1989.

“Alterations in Cell Functions with Ischemia and Shock and Their Correction”, Arch. Surg. (Chicago). 1981.


Kyowa Hakko Publication on Japan’s Statement of Classifications no. 81392.
“Functional & Metabolic Effects of Adenosine in Cardioplegia:

Role of Temperature & Concentration”, Annals. of Thor. Surg., 1997.


Di Pasquale, Mauro, M.D., Amino Acids and Proteins for the Athlete, The Anabolic Edge, 1997.


Bailey, Shannon M., Cynthia G. Van Horn, and Carol C. Cunningham. "Chronic Ethanol Consumption Decreases Mitochondrial and Glycolytic Production of ATP in Liver."

Alcohol & Alcoholism. By Tracey A. Young. Vol. 41. Oxford: Oxford University, 2006. 254-60. Print. Ser. 3.

*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.



Who is the Developer of
Montiff ATP
Adenosine Triphosphate?

Montiff's President and product formulator, Don Tyson has over 50 years in medical technology and use of ion-exchange chromatography to analyze amino acids content of plasma and urine. He is the formulator of all Montiff products.

This man has been my mentor for over 12 years. He never fails in his impeccable integrity and boundless caring and compassion.


Ellen Landauer is an expert with over 40 years in-depth study and experience of the safe and effective use of nutritional supplements, botanical extracts and detoxification methods.

She is Certified as an Advanced Practitioner of Structural Integration body therapy developed by Dr. Ida P. Rolf - also known as Rolfing. This hands-on therapy is the deepest, most comprehensive body alignment therapy. 


Ellen Landauer is also a NEWLY PUBLISHED AUTHOR!


To learn more about Ellen Landauer, see her detailed bio HERE



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Throughout this website, statements are made pertaining to the properties and/or functions of food and/or nutritional products. These statements have not been evaluated by the FDA and these materials and products are not intended to diagnose, treat, cure or prevent any disease. For all health and medical questions, please consult with your doctor. By viewing this site, you are stating that you agree with this disclaimer.


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