ThermoLife T-Bol

150 Capsules
 $74.99 $49.99
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What's in ThermoLife T-Bol?
150 Capsules
Supplement Facts
Serving Size2Capsules
Servings Per Container75
Amount Per Serving% Daily Value
Alatusterone™ T. Alatus (Patent Pending Proprietary Extract)100mg
Divanabol™ Urtica Dioica300mg
((Pharmaceutical Standards Compliant Standardized Extract, Containing SHBG Binding Lignans 3,4-Divanillyltetrahydrofuran, Neoolivil, (-)-Secoisolariciresinol, Dehydrodiconiferyl Alcohol, And Isolariciresinol)
Testveratrol™ Giant Knotweed Rhizome (50% Resveratrol)200mg
Testafolia™ Eurycoma Longifolia100mg
(Aqueous Extraction Standardized For Our Proprietary Blend Of: Eurycomanone, Eurycomalactone, 13-A (21)-Epoxyeurycomanone, Methoxycanthin-6-One, B-Carboline-1-Propioic Acid)
Lectosorb™ Lecithin100mg
Forskobolin™ (Coleus Forskohlii Standardized To 20% Forskolin)40mg
BZATD™ (Zinc Amino Acid Chelate)10mg
ResoProtect™ Bioperine®5mg
Other Ingredients
Rice Powder, And Magnesium Stearate.

Directions For ThermoLife T-Bol: As an adult dietary supplement for natural testosterone enhancement take 3 capsules with 8 ounces of water twice daily, preferably on an empty stomach. Take one serving in the morning and another in the evening. For best results take one serving before a workout.

Warnings: Do not exceed 6 capsules per day. Consult a physician before using this or any new dietary supplement. Not for use for persons under 18 years of age. Do not take if you are female, especially if pregnant or breast feeding, chronically ill, or taking any prescription or over-the-counter medicine, including but not limited to antidepressants (such as MAO inhibitors), stimulants, allergy medications, and medications for high blood pressure or other cardiovascular conditions. Discontinue use and call your physician if you experience any adverse side effects.

* 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.


ThermoLife T-Bol

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T-Bol

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Lifting the unliftable. This is androbolic pull: Attracting the things you want. Drawing you closer to your goals. Igniting a towering androgen inferno inside of you with testosterone on top. A metabolism more intensely anabolic than any muscle-building challenge could possibly require. Catalyzing serial physique transformations from big to bigger to massive to surreal.

ThermoLife Deadlift Picture

From ThermoLife, the industry source of the highest end body-building nutracologicals, comes T-BOL™, a boldly aggressive testosterone up-regulating formula which elevates and sustains endogenous production of testosterone and related androgens. Luxuriously pure and concentrated, it handles even the most brutal training regimes. Ideal for hardgainers and overtrainers. Makes you twice the athlete you used to be. Driven by eight pharmacologically active nutrients (nutracologicals) including Tribulus alatus (patent pending testosterone up-regulator), resveratrol (cardio protective anti-estrogen) and Urtica dioica (increases free testosterone). Thousands of satisfied customers and industry insiders around the world know T-BOL™ represents the highest end of endogenous testosterone up-regulating formulas. Get T-BOL™ today and give yourself the "androbolic pull" you need to build your best body ever.

T- BOL™ the exciting new natural testosterone augmenter and sexual performance enhancer has finally arrived.

T-BOL Maximum Strength Testosterone Enhancement Formula is the most comprehensive and powerful natural testosterone boosting formula ever developed. T-BOL works synergistically with your body's own endocrine system to naturally increase testosterone levels. Featuring a brand new STB (super testosterone booster) that raised testosterone levels in clinical studies more than any natural testosterone booster ever sold. This remarkable ingredient is combined with the most effective natural ingredients known to man for increasing the body's capacity to produce more of its own testosterone.

T-BOL works by stimulating the testosterone production centers of your endocrine system to produce more testosterone. In other words, T-BOL turns on the switch that tells your body to make testosterone and keeps it on! In addition T-BOL also enables your body to use the extra testosterone more efficiently by freeing bound testosterone and increasing receptor sensitivity. T-BOL will restore and BOOST your body's own testosterone production way beyond what your body can produce on its own (without T-BOL). As long as you supplement with T-BOL your body will pump out more testosterone into your blood stream where it can help to burn fat, fuel intense workouts, grow new muscle, gain strength, T-BOL can also be used as PCT (post cycle therapy). Continue reading on the following pages for ingredients and complete reference information.

*All ingredients present in pharmacologically significant amounts for pharmacological effects. A Trademark distinction of ThermoLife formulas.

Here are the ingredients we used and why:

Tribulus Alatus
Tribulus Terrestris was used successfully for years in many successful test-boosting products such as Tribosten and ThermoLife was proud to be the first company to isolate the active protodioscin from Tribulus Terrestris and develop a standard for it. However progress moves on and better compounds are always found. So we are proud to introduce to the world the successor of Tribulus Terrestris, Tribulus Alatus, exclusive and patent pending to ThermoLife International. A plant with many beneficial properties, such as hypoglycemic and hypolipidemic(1) , Tribulus Alatus is not only rich in Saponins found also in Tribulus Terrestris but also contains six novel steroidal saponins which S.A.R. research suggests them to be much, much more potent than those found in Tribulus Terrestris(2).

Eurycoma Longifolia (Longjack)
Eurycoma Longifolia is the scientific name of the Malaysian plant Tongkat Ali, also known as Longjack. In Malaysia it is identified as a symbol of a man's ego and strength, as it is used to increase male virility and sexual progress (7). Some of it's other beneficial actions are antiproliferative, antimalarian, antiviral, antihypertensive, antioxidant and anxiolytic (9,10,11,12,13,17). According to his published research studies based on human subjects (43,44,45), Tongkat Ali increased testosterone production in vitro and increased energy and feeling of well being, inhibited SHBG, increased ATP production in muscles and increased lean muscle mass. Despite its outstanding male sexual performance enhancing properties, until now Eurycoma has never made it as a great ingredient in test boosters. That was due to mainly two factors: First, the amount of actives present in all of today's Longjack containing supplements are severely under dosed most of the cheap extracts used are not standardized for the actual actives but standardized for cytotoxic compounds like eurycomanones. ThermoLife uses extract made by prime researchers on Longjack, standardized for concentration of the actual actives with minimum concentration on cytotoxic compounds.

Resveratrol
Resveratrol (3,5,4'-trihydroxystilbene) is a phytoalexin mainly found in red wine. To date it has found many uses due to its many benefits to human health. Such positive effects include strong antioxidant activity, antilipidemic, cardioprotective, antiproliferative, and antiatheroscleretic effects (26,27,28). One great property of this wonderful compound, which has never been put to use up until now is its ability to enhance male potency, sexual health, and strength (when administered in high enough amounts). Overall resveratrol was able to not only increase testosterone. The suggested mechanisms of action are its antiestrogenic effects, as resveratrol is an aromatase inhibitor and also has the capability to antagonistically bind to estrogen receptors. It also has strong antioxidant activities which can counter oxidant stress in the seminiferous tubules, thus protecting the testicle cells (29). Another beneficial action it has is anti-aromatase action both on enzyme and m-RNA levels (32).

Urtica Dioica
Urtica dioica, commonly known as stinging nettle, is a plant that grows aplenty in many Mediterranean countries like Greece and Turkey. It has a long history of use in traditional medicine, as well as being used for food. Examples of it's many beneficial properties are as an analgesic (33), antihyperglycemic (34), antioxidant (35) antiviral (36), Hepatoprotective (37), antihyperlipidemic (38), and an antithrombotic (39) agent. Of interest to bodybuilders is the capacity of certain Urtica Dioica lignans to bind with human sex hormone binding globulin (SHBG) (40,41,42). This effect results in the release of testosterone from SHBG, which makes it much more available for interaction with cells in order for it to exert its beneficial effects. Although we can't claim novelty with this compound since it's already available in quite a few successful products, ThermoLife is proud to continue with it's top quality standards by using a powerful 97% extract.

Forskolin
Forskolin is a labdane diterpene that is produced by the Indian Coleus plant (Plectranthus barbatus). Forskolin has a favorable effect on enhancing serum testosterone levels through it's potential influence on cAMP. Because LH exerts its effects on Leydig cells of the testicles (stimulating production of testosterone) through cAMP, an increase in testosterone levels using this compound is exhibited as well(43,44). In fact Forskolin is commonly used in studies to stimulate testosterone production from Leydig cells (45,46). Apart from this Forskolin exhibits a beneficial effect on reducing fat levels while increasing lean muscle mass.

Zinc
Zinc was added to the matrix because it's a mineral that is necessary for the body to create testosterone. Many males intake a lower amount of Zinc than is optimal for testosterone production, therefore preventing their body's from performing at their natural optimal testosterone producing capabilities. This means that the rest of T-BOL's stellar ingredients wouldn't be able to give the maximum results in such zinc deficient men, and to counter this 10mg of Zinc in a most bioavailable form (Glycine chelate) was added.

Lecithin
All steroidal compounds, like the steroidal saponins found in T Alatus need to be dissoluted in bile to be absorbed by the intestines. The presence of even small amountsof lecithin can increase the dissolution rates up to tenfold (47).

T-BOL Body Composition Graphs

Bioperine
Bioperine is a patented piperine extract. Piperine has the capability of blocking glucuronidation(48), a main metabolic pathway that both lowers intestinal absorption and increases excretion, thus lowering the efficacy of many compounds present in T-BOL.

In Conclusion
T-BOL is specifically made to hit all possible aspects of androgen-enhancement, using what we consider to be the absolute best, top quality ingredients in effective doses. We left out what we considered to be ineffective, unneeded, or not worth the price.

To sum everything up so far, the compounds in T-BOL offer benefits such as:

  1. Powerful ingredients each independently proven to increase androgen levels in T-BOL's dosages.
  2. A highly bioavailable form of Zinc, more bioavailable than the one used in ZMA.
  3. ncreases in testosterone releasing hormones LH and FSH.
  4. Increases concentration of other anabolic hormones in the body by increasing concentration and providing precursors.
  5. Protection from free radical damage.
  6. Mild aromatase inhibition.
  7. SHBG production inhibition.
  8. Release of testosterone from SHBG.
  9. Increases intramuscular ATP levels.
  10. Increase energy and mood.
  11. Inhibition of testosterone breakdown.

References

1 Hypoglycemic and hypolipidemic effects of alcoholic extract of Tribulus alatus in streptozotocin-induced rats: a comparative study with T. terrestris (Caltrop).
2 Free serum testosterone level in male rats treated with Tribulus alatus extracts. El-Tantawy WH, Temraz A, El-Gindi OD.Drug Bioavailability Center, National Organization For Drug Control and Research, Cairo, Egypt. wldhmdy@yahoo.com
3 Phytochemistry. 2006 May;67(10):1011-8. Epub 2006 May 2 Steroidal saponins from the aerial parts of Tribulus alatus Del. Temraz A, El Gindi OD, Kadry HA, De Tommasi N, Braca A. Dipartimento di Chimica Bioorganica e Biofarmacia, Università di Pisa, Via Bonanno 33, 56126 Pisa, Italy.
4. Gimlette, J.D. and Thomson, J.W. (eds). “A dictionary of Malaysian medicine.” (1977).
5. Ang HH, et al. “Effects of Eurycoma longifolia jack on laevator ani muscle in both uncastrated and testosterone-stimulated castrated intact male rats.” Arch Pharm Res. 24(5), (2001): Pages 437-40.
6. Ang, H.H. Chan, K.L. and Mak, J.W. J.Ethnopharmacol. 49 (1995): Pages 171-175
7. Bansiddhi J. and Pecharaply D. Botanical Report of Some Thai Medicinal Plants, Department of Medical Sciences, Bangkok, Thailand. (1988): Pages 21-23
8. Chan, K.L. Lee, S.P and Yuen, K.H. “Antipyretic Activity of Quassinoids from Eurycoma Longifolia Jack”. (1995).
9. Morita, H. Kishi, E., Takeya, K. Itokawa, H., and Iitaka, Y. 1993. Chem. Lett. 5:749-752
10. Morita, H. Kishi, E., Takeya, K. Itokawa, H., and Iitaka, Y. 1993 Phytochem 34:765-771
11. Ang HH, et al. “Aphrodisiac evaluation in non-copulator male rats after chronic administration of Eurycoma longifolia Jack.” Fundam Clin Pharmacol. 15(4), (2001): Pages 265-8.
12. Ang HH, et al. “Evaluation of the potency activity of aphrodisiac in Eurycoma longifolia Jack.” Phytother Res. 15(5), (2001): Pages 435-6.
13. Ang HH, et al. “Effects of Eurycoma longifolia Jack (Tongkat Ali) on the initiation of sexual performance of inexperienced castrated male rats.” Exp Anim. 49(1), (2000): Pages 35-8.
14. Ang HH, et al. “Studies on the anxiolytic activity of Eurycoma longifolia Jack roots in mice.” Jpn J Pharmacol. 79(4), (Apr 1999): Pages 497-500.
15. Ang HH, et al. “Eurycoma longifolia Jack enhances sexually experienced male rats.” Exp Anim. 46(4) (Oct 1997): Pages 287-90.
16. Ang HH, et al. “Sexual arousal in sexually sluggish old male rats after oral administration of Eurycoma longifolia Jack.” J Basic Clin Physiol Pharmacol. 15(3-4), (2004): Pages 303-9.
17. Ang HH, et al. “Eurycoma longifolia Jack enhances sexual motivation in middle-aged male mice.” J Basic Clin Physiol Pharmacol. 14(3), (2003): Pages 301-8.
18. Ang HH, “Effects of Eurycoma longifolia Jack on sexual qualities in middle aged male rats.” Phytomedicine. 10(6-7), (2003): Pages 590-3.
19. Ang HH, “Effect of Eurycoma longifolia Jack on orientation activities in middle-aged male rats.” Fundam Clin Pharmacol. 16(6), (Dec 2002): Pages 479-83.
20. Ang HH, et al. “Effect of Eurycoma longifolia Jack in middle-aged male rats.” J Basic Clin Physiol Pharmacol. 13(3), (2002): Pages 249-54.
21. Low BS, “Bioavailability and pharmacokinetic studies of eurycomanone from Eurycoma Longifolia.” Planta Med. 71(9), (Sep 2005): Pages 803-7.
22. Chan KL, et al. “Semisynthetic 15-O-acyl- and 1,15-di-O-acyleurycomanones from Eurycoma longifolia as potential antimalarials.” Planta Med. 71(10), (Oct 2005): Pages 967-9.
23. Belguendouz L., et al. “Resveratrol inhibits metal ion-dependent and independent peroxidation of orcine low-density lipoproteins.” Biochem.Pharmacol., 53(9) (May 1997): Pages 1347��"1355.
24. Bertelli A.A, et al. “Resveratrol, a natural stilbene in grapes and wine, enhances intraphagocytosis in human promonocytes: a cofactor and chemopreventive activity.” Int. J. Tissue React., 21, (1999): Pages 93��"104.
25. Ewa Ignatowicz, Wanda Baer-Dubowska. “RESVERATROL, A NATURAL CHEMOPREVENTIVE AGENT AGAINST DEGENERATIVE”. Polish journal of pharmacology, 53(6), (2001): Pages 557-569.
26. Juan ME, et al. “Trans-Resveratrol, a Natural Antioxidant from Grapes, Increases Output in Healthy Rats” J. Nutr. 135(4), (Apr 2005): Pages 757��"760.
27. Piver B, et al. “Differential inhibition of human cytochrome P450 enzymes by epsilon-viniferin, the dimer of resveratrol: comparison with resveratrol and polyphenols from alcoholized beverages.” Life Sci. 73(9), (Jul 2003): Pages 1199-213.
28. Piver B, et al. “Inhibition of CYP3A, CYP1A and CYP2E1 activities by resveratrol and other non volatile red wine components.” Toxicol Lett. 125(1-3), (Dec 2001): Pages 83-91.
29. Wang Y, et al. “The red wine polyphenol resveratrol displays bilevel inhibition on aromatase in breast cells.” Toxicol Sci. 92(1), (Jul 2006): Pages 71-7.
30. Randall C, et al. “Randomized controlled trial of nettle sting for treatment of base-of-thumb.” J R Soc Med. 93(6), (Jun 2000): Pages 305-9.
31. Bnouham M, et al. “Antihyperglycemic activity of the aqueous extract of Urtica dioica.” Fitoterapia. 74(7-8), (Dec 2003): Pages 677-81.
32. Cetinus E, et al. “The role of urtica dioica (urticaceae) in the prevention of oxidative stress caused by tourniquet application in rats.” Tohoku J Exp Med. 205(3), (Mar 2005): Pages 215-21.
33. Uncini Manganelli RE, et al. “Antiviral activity in vitro of Urtica dioica L., Parietaria diffusa M. et K. and Sambucus nigra L.” J Ethnopharmacol. 98(3), (Apr 2005): Pages 323-7.
34. Kanter M, et al. “Hepatoprotective effects of Nigella sativa L and Urtica dioica L on lipid peroxidation, antioxidant enzyme systems and liver enzymes in carbon tetrachloridetreated rats.” World J Gastroenterol. 11(42), (Nov 2005): Pages 6684-8.
35. Daher CF, et al. “Effect of Urtica dioica extract intake upon blood lipid profile in the rats.” Fitoterapia. 77(3), (Apr 2006): Pages 183-8.
36. El Haouari M, et al. “Inhibition of rat platelet aggregation by Urtica dioica leaves extracts.” Phytother Res. 20(7), (Jul 2006): Pages 568-72.
37. Gansser D, et al. “Plant constituents interfering with human sex hormone-binding globulin. Evaluation of a test method and its application to Urtica dioica root extracts.” Z Naturforsch [C]. 50(1-2), (Jan-Feb 1995): Pages 98-104.
38. Schottner M, et al. “Lignans from the roots of Urtica dioica and their metabolites bind to human sex hormone binding globulin (SHBG).” Planta Med. 63(6), (Dec 1997): Pages 529-32.
39. Hryb DJ, “The effect of extracts of the roots of the stinging nettle (Urtica dioica) on the interaction of SHBG with its receptor on human prostatic membranes.” Planta Med. 61(1), (Feb 1995): Pages 31-2.
40. Chris Kilham. “Ali is the Greatest.” Physical Magazine, (Mar 2004).
41. Chris Kilham. “Tongkat Ali: Sexual Treasure of Southeast Asia.” Let's Live, (Feb 2004).
42. “Jungle Herbs: Rev Up Romance.” Prevention Magazine, (Nov 2003).
43. Valenti, S, Guido, R, Giusti, M, Giordano, G. (1995) In vitro acute and prolonged effects of melatonin on purified rat Leydig cell steroidogenesis and adenosine 3',5'-monophosphate production Endocrinology 136,5357-5362 [Abstract]
44. Valenti, S, Fazzuoli, L, Giordano, G, Giusti, M. (2001) Changes in binding of iodomelatonin to membranes of Leydig cells and steroidogenesis after prolonged in vitro exposure to melatonin Int J Androl. 24,80-86 [Medline]
45. Serotonin secretion from rat Leydig cells.Tinajero JC, Fabbri A, Ciocca DR, Dufau ML.Section on Molecular Endocrinology, National Institute of Child Health and Human Development, National Institute of Health, Bethesda, MD 20892.
46. Expression of testicular 3 beta-hydroxysteroid dehydrogenase/delta 5----4-isomerase: regulation by luteinizing hormone and forskolin in Leydig cells of adult rats. Keeney DS, Mason JI. Cecil H. and Ida Green Center for Reproductive Biology Sciences, Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas 75235-9051.
47. Dissolution of steroids in bile salt solutions is modified by the presence of lecithinAuteur(s) / Author(s) NAYLOR L. J. (1) ; BAKATSELOU V. ; RODRIGUEZ-HORNEDO N. ; WEINER N. D. ; DRESSMAN J. B. ; Affiliation(s) du ou des auteurs / Author(s) Affiliation(s) Abbott Laboratories, North Chicago IL, ETATS-UNIS
48. J Pharmacol Exp Ther. 1986 Feb;236(2):488-93. Piperine-mediated inhibition of glucuronidation activity in isolated epithelial cells of the guinea-pig small intestine: evidence that piperine lowers the endogeneous UDP-glucuronic acid content.
49. Body Composition and Hormonal Adaptations Associated with Forskolin Consumption in Overweight and Obese Men. Michael P. Godard, Brad A. Johnson and Scott R. Richmond. Obesity Research (2005) 13, 1335��"1343; doi: 10.1038/oby.2005.162

 

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