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A Synergistically Designed Menopause Type® Formulation

Formulation Focus

testo-calm

A Unique Blend of Phytoantiandrogens
and other Herbs to Naturally Support Hormonal Balance.

Designed for women with menopause symptoms associated with excessive testosterone function, such as Menopause Types® 3, 6, 9 & 12.

How Women Will Benefit From testo-Calm™

  • Promote Normal, Healthy Androgen Function.
  • Support Healthy Glucose Homeostasis.
  • Supports Healthy Blood Lipid Levels, Including Triglycerides.
  • Promotes Healthy Immune Function, Supporting Anti-Inflammatory Activity.
  • Helps Normalize the Function of Skin, Heart, Breasts, Brain and other Tissues Sensitive to Testosterone.
  • Supports Healthy Brain Function, Memory, and Cognition, Enhances Mood While Promoting Tranquility.

 

Synergistic Formulation:

testo-Calm™ is a synergistic designed formula developed to promote healthy hormone balance in women by calming and supporting the ideal function of testosterone sensitive tissues. (Excessive affects of the hormone testosterone in women is associated with hirsutism, acne, androgenic alopecia as well as mood changes, insulin resistance, elevated blood lipids and increased risk of breast, endometrial and possibly other cancers. The affect may be due to either androgen excess or increased sensitivity to normal levels of androgens.)

Decreasing the sensitivity to excessive androgen levels can support the healthy function of skin, hair, heart, breasts, vagina and other testosterone sensitive tissues and may promote optimal structure and function of these tissues, which can result in an improvement of perimenopause, menopause and postmenopause symptoms.

Three Capsules Provide:

testo-calm™ Herbal Blend

2,160 mg

(propriety blend of Saw Palmetto (berry, standardized to 25% fatty acids), Fennel (Foeniculum vulgare, seed), Nettles (leaf, standardized to 1% plant silica), Ocimum sanctum (leaf), Trigonella foenum-graecum (seed) and Pygeum africanum (bark, standardized to 12% phytosterols)

Suggested Use:

90 Capsules

As a dietary supplement, adults take 3 capsules each morning with food or as directed by physician.

 

ABOUT Phytoantiandrogens: Phytoantiandrogens are a class of phyto-compounds that decrease tissue sensitivity to androgens or decrease androgen activity, predominantly through the action of 5-alpha-reductase inhibition, which decreases conversion of testosterone to the more androgenic dihydrotestosterone. Androgen excess symptoms have been observed in Menopause Types® 3, 6, 9 & 12. Androgen excess disorders have also been observed in polycystic ovary disease (PCO) and PCO-like syndrome, which has a milder clinical presentation than PCO. Even though PCO & PCO-like syndrome occur in young women, associated insulin resistance, lipid disorders and cancer risks have also been observed, revealing that these factors are not exclusively age related.

Saw Palmetto: Saw Palmetto (Serenoa repens) is widely used for the antiandrogenic properties attributed to it, which are most likely due to the presence of beta-sitosterol, palmitic-acid and stearic-acid, all of which have 5-alpha-reductase inhibiting activity. The anti-inflammatory properties have recently been noted in Serenoa repens may be associated with its beneficial properties.

Fennel: Fennel (Foeniculum Vulgare) seed is a source of the antiandrogens Palmetic acid and beta-sitosterol active components within many antiandrogenic herbs. The androgen antagonist properties of Foeniculum Vulgare have been used for women in topical agents to control hirsutism. In animal studies, fennel extracts have demonstrated antitumor activity in testosterone sensitive tissue.

Nettles: Nettles (Urtica dioica) has the antiandrogen palmetic acid as an active component within the herb. Antihyperglycemic and hypoglycemic effects have also been noted in Urtica dioica. Anti-inflammatory, analgesic and antioxidant properties have been attributed to Urtica dioca which contribute to its beneficial properties.

Holy Basil: Holy Basil (Ocimum sanctum) leaf, with a long history of use in Ayurvedic Medicine, contains antiandrogenic properties that may be attributed to the presence of the 5-alpha-reductase inhibiting constituents; beta-sitosterol, palmitic-acid and stearic-acid. In animal studies the anti-androgenic property of Ocimum Sanctum was shown to diminish response in androgen sensitive tissues, an effect that was reversible two weeks after the extract was stopped. Antihyperglycemic and hypoglycemic effects has also been noted in Holy Basil. Animal studies have shown Ocimum sanctum can cause lowering in serum total cholesterol, triglyceride, phospholipid and LDL-cholesterol levels and an increase in the HDL-cholesterol. Sedative properties have been identified in Ocimum sanctum as well as adaptogenic and antistressor properties in regard to adverse stimuli and toxic substances. Ocimum sanctum has also been found to inhibit acute as well as chronic inflammation in animal studies, which may contribute to its antistress, adaptogenic properties.

Fenugreek: Fenugreek (Trigonella foenum-graecum) seed has antiandrogenic properties due to the presence of beta-sitosterol, palmitic-acid and stearic-acid. Beneficial anti-hyperglycemic and hypoglycemic properties of Trigonella Foenum-Graecum have been shown to decrease elevated glucose in a double blind placebo controlled human study. It has been shown to reduce excessive glucose levels and increase the number of insulin receptors in humans, possible by stimulating glucose-dependent insulin secretion from pancreatic beta cells. Both human and animal studies have shown Fenugreek has the ability to lower total cholesterol, LDL, VLDL cholesterol and triglycerides significantly. Anti-inflammatory properties have also been documented in Trigonella Foenum Graecum, contributing to its beneficial properties.

Pygeum: Pygeum (Pygeum africanum) bark has the antiandrogen beta-sitosterol. Anti-inflammatory properties have been noted in Pygeum Africanum contributing to the beneficial properties.

 

References:

Ahmed M, Ahamed RN, Aladakatti RH, Ghosesawar MG. Reversible anti-fertility effect of benzene extract of Ocimum sanctum leaves on sperm parameters and fructose content in rats. J Basic Clin Physiol Pharmacol. 2002;13(1):51-9.

Ajabnoor MA, Tilmisany AK. Effect of Trigonella foenum graceum on blood glucose levels in normal and alloxan-diabetic mice. J Ethnopharmacol 1988;22:45-49.

Anon. 1948-1976. The Wealth of India raw materials. Publications and Information Directorate, CSIR, New Delhi. 11 volumes.

Breu W, Hagenlocher M, Redl K, Tittel G, Stadler F, Wagner H. [Anti-inflammatory activity of sabal fruit extracts prepared with supercritical carbon dioxide. In vitro antagonists of cyclooxygenase and 5-lipoxygenase metabolism] Arzneimittelforschung. 1992 Apr;42(4):547-51. German.

Collins, JJ. 2002. Discover Your Menopause Type. Prima Publishing Rocklin, CA

Collins, Joseph J. 2002. Discover Your Menopause Type. Prima Publishing Rocklin, CA

Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press

Godhwani S, Godhwani JL, Vyas DS. Ocimum sanctum: an experimental study evaluating its anti-inflammatory, analgesic and antipyretic activity in animals. J Ethnopharmacol. 1987 Nov;21(2):153-63.

Gulcin I, Kufrevioglu OI, Oktay M, Buyukokuroglu ME. Antioxidant, antimicrobial, antiulcer and analgesic activities of nettle (Urtica dioica L.). J Ethnopharmacol. 2004 Feb;90(2-3):205-15.

Gupta A, Gupta R, Lal B. Effect of Trigonella foenum-graecum (fenugreek) seeds on glycaemic control and insulin resistance in type 2 diabetes mellitus: a double blind placebo controlled study. J Assoc Physicians India. 2001 Nov;49:1057-61.

Hannan JM, Rokeya B, Faruque O, Nahar N, Mosihuzzaman M, Azad Khan AK, Ali L. Effect of soluble dietary fibre fraction of Trigonella foenum graecum on glycemic, insulinemic, lipidemic and platelet aggregation status of Type 2 diabetic model rats. J Ethnopharmacol. 2003 Sep;88(1):73-7.

Javidnia K, Dastgheib L, Mohammadi Samani S, Nasiri A. Antihirsutism activity of Fennel (fruits of Foeniculum vulgare) extract. A double-blind placebo controlled study. Phytomedicine. 2003;10(6-7):455-8.

Kantak NM, Gogate MG. Effect of short term administration of Tulsi (Ocimum sanctum Linn.) on reproductive behaviour of adult male rats. Indian J Physiol Pharmacol. 1992 Apr;36(2):109-11.

Kelm MA, Nair MG, Strasburg GM, DeWitt DL. Antioxidant and cyclooxygenase inhibitory phenolic compounds from Ocimum sanctum Linn. Phytomedicine. 2000 Mar;7(1):7-13.

Ng SS, Figg WD. Antitumor activity of herbal supplements in human prostate cancer xenografts implanted in immunodeficient mice. Anticancer Res. 2003 Sep-Oct;23(5A):3585-90.
Mavi A, Terzi Z, Ozgen U, Yildirim A, Coskun M. Antioxidant properties of some medicinal plants: Prangos ferulacea (Apiaceae), Sedum sempervivoides (Crassulaceae), Malva neglecta (Malvaceae), Cruciata taurica (Rubiaceae), Rosa pimpinellifolia (Rosaceae), Galium verum subsp. verum (Rubiaceae), Urtica dioica (Urticaceae). Biol Pharm Bull. 2004 May;27(5):702-5.

Paubert-Braquet M, Cave A, Hocquemiller R, Delacroix D, Dupont C, Hedef N, Borgeat P. Effect of Pygeum africanum extract on A23187-stimulated production of lipoxygenase metabolites from human polymorphonuclear cells. J Lipid Mediat Cell Signal. 1994 May;9(3):285-90.

Petit P, Sauvaire Y, Ponsin G, Manteghetti M, Fave A, Ribes G. Effects of a fenugreek seed extract on feeding behaviour in the rat: metabolic-endocrine correlates. Pharmacol Biochem Behav. 1993 Jun;45(2):369-74.

Prager N, Bickett K, French N, Marcovici G. A randomized, double-blind, placebo-controlled trial to determine the effectiveness of botanically derived inhibitors of 5-alpha-reductase in the treatment of androgenetic alopecia. J Altern Complement Med. 2002 Apr;8(2):143-52.

Raghuram TC, Sharma RD, Sivakumar B, et al. Effect of fenugreek seeds on intravenous glucose disposition in non-insulin dependent diabetic patients. Phytother Res 1994;8:83-86.

Sakina MR, Dandiya PC, Hamdard ME, Hameed A. Preliminary psychopharmacological evaluation of Ocimum sanctum leaf extract. J Ethnopharmacol. 1990 Feb;28(2):143-50.

Sarkar A, Lavania SC, Pandey DN, Pant MC Changes in the blood lipid profile after administration of Ocimum sanctum (Tulsi) leaves in the normal albino rabbits.Indian J Physiol Pharmacol. 1994 Oct;38(4):311-2.

Schulze-Tanzil G, de SP, Behnke B, Klingelhoefer S, Scheid A, Shakibaei M. Effects of the antirheumatic remedy hox alpha--a new stinging nettle leaf extract--on matrix metalloproteinases in human chondrocytes in vitro. Histol Histopathol. 2002 Apr;17(2):477-85.

Sembulingam K, Sembulingam P, Namasivayam A. Effect of Ocimum sanctum Linn on noise induced changes in plasma corticosterone level.Indian J Physiol Pharmacol. 1997 Apr;41(2):139-43.

Sen P, Maiti PC, Puri S, Ray A, Audulov NA, Valdman AV Mechanism of anti-stress activity of Ocimum sanctum Linn, eugenol and Tinospora malabarica in experimental animals. Indian J Exp Biol. 1992 Jul;30(7):592-6.

Sharma RD, Raghuram TC, Rao NS. Effect of fenugreek seeds on blood glucose and serum lipids in type I diabetes. Eur J Clin Nutr. 1990 Apr;44(4):301-6.

Singh S, Majumdar DK. Effect of Ocimum sanctum fixed oil on vascular permeability and leucocytes migration. Indian J Exp Biol. 1999 Nov;37(11):1136-8.

Stark A, Madar Z. The effect of an ethanol extract derived from fenugreek (Trigonella foenum-graecum) on bile acid absorption and cholesterol levels in rats.Br J Nutr. 1993 Jan;69(1):277-87.

Sur P, Das M, Gomes A, Vedasiromoni JR, Sahu NP, Banerjee S, Sharma RM, Ganguly DK. Trigonella foenum graecum (fenugreek) seed extract as an antineoplastic agent. Phytother Res. 2001 May;15(3):257-9.

Urman B, Pride SM, Yuen BH. Elevated serum testosterone, hirsutism, and virilism associated with combined androgen-estrogen hormone replacement therapy. Obstet Gynecol. 1991 Apr;77(4):595-8.

 

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.

 

Formulated by:

YourMenopauseType.com, Inc.

Lawrenceville, GA 30044

www.YourMenopauseType.com

 

YourMenopauseType.com, Inc.
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