Man The F%#K Up

Description

With each passing decade, Americans have been getting weaker and men’s testosterone levels have decreased – for the past 3 generations, son’s testosterone levels are lower than their fathers. Whether the cause be plastics, food supply, or the stress of dealing with Liberal bulls#%t, it doesn’t really matter. The power of America is in its citizens – make yourself greater with Man The F#%K Up Body Recomposition & Hardening Agent.

• KSM-66® Ashwagandha increases testosterone levels and muscle mass while decreasing body fat.*
• Primavie® Shilajit enhances testosterone’s ability to build muscle by increasing free testosterone.*
• Laxopure™ 5α-Laxogenin is a novel brassinosteroid providing huge increases in muscle hypertrophy for a hard, defined look.*
• Phosphatidylcholine improves lipolysis and fat-burning.*
• Bioperine® supports optimal absorption of MTFU’s powerful ingredients.*

Testosterone makes everything better. Use Man The F#%K Up to improve your progress in the gym towards a lean, muscular, and strong physique. The ingredient profile has been carefully selected by American scientists for precise synergism to maximize anabolic hormone status, cortisol control, muscle building potential, muscle protein synthesis, type II fiber hypertrophy, and extreme lipolysis. Man The F#%K Up today, and make gains like there is no tomorrow.

*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.

Supplement Facts

Ingredient Profile

Boron (100mg)

Boron is a trace mineral present in nuts and fruits capable of augmenting sex hormones and joint health.

• Daily consumption of boron for 6 days produced marked increases in free testosterone in a study by Naghii et al.
• Has also been demonstrated to reduce estrogen and SHBG for a big boost to the anabolic milieu
• May reduce inflammation and joint pain.

Zinc (75mg)

Zinc is one of the minerals necessary for human survival, abundant in meat and seafood.

• High doses of zinc (MTFU contains 500% DV) inhibit the aromatase enzyme, increasing testosterone and decreasing estrogen.
• Helps to repair the intestinal mucosa, which may improve nutrient absorption and decrease bloating.
• Zinc is lost in sweat, and it is therefore an important mineral of which to maintain proper consumption.

Potassium (300mg)

Potassium is an essential mineral needed in the largest quantities of all minerals at over 4g per day.

• Due to such high requirements and often poor diets, low potassium status can decrease testosterone production.
• Important for counteracting the hypertensive effects of sodium – potassium facilitates excess sodium excretion.

Vitamin B6 (20mg)

Vitamin B6 is one of the water soluble B vitamins that is critical for various metabolic reactions that occur in the body. It is also a coenzyme for protein metabolism and nervous and immune system function.

• Vitamin B6 may have some benefits with regard to increasing the rate of testosterone synthesis by accelerating conversion of prohormones into testosterone.
• B6 is also involved in the formation of the most important enzymes for a well-functioning metabolism
• B6 may also be able to increase levels of growth hormone.

Vitamin C (250mg)

Vitamin C is a water soluble vitamin with antioxidant and immunomodulatory potential.

• As a potent antioxidant, vitamin C can preserve testosterone concentrations in response to lead toxicity, burns, and alcohol ingestion amongst other factors.
• Exhibits cortisol controlling effects, potentially reducing body fat.
• Can accelerate recovery from the common cold and prevent the occurrence of colds when used preemptively.

Vitamin D3 (2500IU)

Vitamin D is associated with a wide range of benefits, including increased cognition, immune health, bone health and well-being.

• Vitamin D may increase testosterone levels after supplementation by serving as cholesterol-like precursor to testosterone or other mechanisms.
• Supplementation can also reduce the risks of cancer, heart disease, diabetes and multiple sclerosis.

KSM-66® Ashwagandha (500mg)

Ashwagandha is an ancient ayurvedic herb and adaptogen. KSM-66® is a standardized version that can be trusted to contain necessary quantities of active ingredients.

• Supplementation with Ashwagandha has been demonstrated to improve testosterone levels in healthy men.
• Increased testosterone by Ashwagandha is thought to be the underlying mechanism for improved strength and lean mass and decreased fat mass after Ashwagandha supplementation.
• Doubles as a potent anxiolytic agent to reduce cortisol and anxiety.

Primavie® Purified Shilajit Extract (250mg)

Shilajit is a mixture of minerals and other chemicals, principally fulvic acid, that has testosterone boosting and antioxidant properties. Primavie® contains a standardized quantity of fulvic acid.

• One study has observed a 23.5% increase in testosterone in men after they begin supplementing with shilajit.
• Works to improve blood lipid parameters, including decreased triglycerides.

Laxopure™ (100mg)

Laxopure™ 5α-Hydroxy-Laxogenin is a natural anabolic derived from plants.  It is a sapogenin, a steroidal constituent of a saponin.

• 5-Alpha-Hydroxy-Laxogenin possesses an anabolic potency similar to Anavar, one of the most efficient anabolic substances, without side effects.
• May work by reducing sex hormone binding globulin (SHBG) hormones to increase free testosterone.
• Research in humans has shown 5-Alpha-Hydroxy-Laxogenin increases muscle strength and lean body mass, even without exercise. Other benefits include fat loss and improved insulin sensitivity.
• Other tests have shown 200% increases in protein synthesis after 5-Alpha-Hydroxy-Laxogenin supplementation.

Phosphatidylcholine (25mg)

Phosphatidylcholine is a phospholipid present in the cellular membrane that helps with membrane fluidity.

• Phosphatidylcholine serves as a source of choline, which boosts cognition and power output.
• phosphatidylcholine has traditionally been used for inducing lipolysis in fat cells for reductions in body fat mass.

Bioperine® Black Pepper Extract (5mg)

Bioperine® is a high quality piperine extract. Piperine boosts absorption of herbal ingredients.

• Inhibits glucuronide to boost uptake of many herbal supplements and some drugs.
• May slow gastric emptying and provide a mild satiety effect as well as enhanced absorption via increased contact time between food and intestinal lining.

FAQ

Q: What is the best way to use Man The F#%K Up®?

A: As a dietary supplement, take one serving (3 capsules) in the morning with food. For best results, use 2 servings per day for 8 weeks, then take a 4 week break before starting a new cycle.

Q: Should I Stack Man The F#%K Up® with any other Liberty Labz products?

A: Man The F#%K Up® is a powerful muscle builder with fat loss agents, but there is nothing as effective as a good gym session. Pair Man The F#%K Up® with Stand The F#%K Up Pre-workout for the ultimate anabolic punch.

Q: How does Man The F#%K Up® boost testosterone?

A: Man The F#%K Up® contains several testosterone boosting ingredients with unique mechanisms of action. The main ingredient, KSM-66® Ashwagandha has been proven to increase testosterone levels in healthy men. Ashwagandha acts as a GABA-mimetic on the hypothalamus, releasing gonadotropin-releasing hormone, which stimulates the pituitary to release luteinizing hormone (LH). LH then triggers the testes to start producing testosterone.

References

Boron

1. Naghii, M. R., Mofid, M., Asgari, A. R., Hedayati, M., & Daneshpour, M. S. (2011). Comparative effects of daily and weekly boron supplementation on plasma steroid hormones and proinflammatory cytokines. Journal of trace elements in medicine and biology, 25(1), 54-58.
2. Naghii, M. R., & Samman, S. (1996). The effect of boron supplementation on the distribution of boron in selected tissues and on testosterone synthesis in rats. Journal of nutritional biochemistry, 7(9), 507-512.
3. Lee, I. P., Sherins, R. J., & Dixon, R. L. (1978). Evidence for induction of germinal aplasia in male rats by environmental exposure to boron. Toxicology and applied pharmacology, 45(2), 577-590.
4. Naghii, M. R., & Samman, S. (1997). The effect of boron supplementation on its urinary excretion and selected cardiovascular risk factors in healthy male subjects. Biological trace element research, 56(3), 273-286.
5. Militaru, C., Donoiu, I., Craciun, A., Scorei, I. D., Bulearca, A. M., & Scorei, R. I. (2013). Oral resveratrol and calcium fructoborate supplementation in subjects with stable angina pectoris: effects on lipid profiles, inflammation markers, and quality of life. Nutrition, 29(1), 178-183.

Zinc

1. Rodondi, A., Ammann, P., Ghilardi-Beuret, S., & Rizzoli, R. (2009). Zinc increases the effects of essential amino acids-whey protein supplements in frail elderly. JNHA-The Journal of Nutrition, Health and Aging, 13(6), 491-497.
2. Ertekin, M. V., Koç, M., Karslioǧlu, I., & Sezen, O. (2004). Zinc sulfate in the prevention of radiation-induced oropharyngeal mucositis: a prospective, placebo-controlled, randomized study. International Journal of Radiation Oncology* Biology* Physics, 58(1), 167-174.
3. Kilic, M. (2007). Effect of fatiguing bicycle exercise on thyroid hormone and testosterone levels in sedentary males supplemented with oral zinc. Neuro endocrinology letters, 28(5), 681-685.
4. Jalali, G. R., Roozbeh, J., Mohammadzadeh, A., Sharifian, M., Sagheb, M. M., Jahromi, A. H., … & Afshariani, R. (2010). Impact of oral zinc therapy on the level of sex hormones in male patients on hemodialysis. Renal failure, 32(4), 417-419.
5. Netter, A., Nahoul, K., & Hartoma, R. (1981). Effect of zinc administration on plasma testosterone, dihydrotestosterone, and sperm count. Archives of andrology, 7(1), 69-73.
6. Kilic, M., Baltaci, A. K., Gunay, M., Gökbel, H., Okudan, N., & Cicioglu, I. (2006). The effect of exhaustion exercise on thyroid hormones and testosterone levels of elite athletes receiving oral zinc. Neuro endocrinology letters, 27(1-2), 247-252.
7. Solati, Z., Jazayeri, S., Tehrani-Doost, M., Mahmoodianfard, S., & Gohari, M. R. (2015). Zinc monotherapy increases serum brain-derived neurotrophic factor (BDNF) levels and decreases depressive symptoms in overweight or obese subjects: a double-blind, randomized, placebo-controlled trial. Nutritional neuroscience, 18(4), 162-168.

Potassium

1. Sánchez-Capelo, A., Castells, M. T., Cremades, A., & Peñafiel, R. (1996). Hypokalemia decreases testosterone production in male mice by altering luteinizing hormone secretion. Endocrinology, 137(9), 3738-3743.
2. Whelton, P. K., He, J., Cutler, J. A., Brancati, F. L., Appel, L. J., Follmann, D., & Klag, M. J. (1997). Effects of oral potassium on blood pressure: meta-analysis of randomized controlled clinical trials. Jama, 277(20), 1624-1632.

Vitamin B6

1. Czaja, J., Lebiedzinska, A., Marszall, M., & Szefer, P. (2011). Evaluation for magnesium and vitamin B6 supplementation among Polish elite athletes.Roczniki Państwowego Zakładu Higieny, 62(4).
2. Manore, M. M. (2000). Effect of physical activity on thiamine, riboflavin, and vitamin B-6 requirements. The American journal of clinical nutrition, 72(2), 598s-606s.
3. Allgood, V. E., & Cidlowski, J. A. (1992). Vitamin B6 modulates transcriptional activation by multiple members of the steroid hormone receptor superfamily. Journal of Biological Chemistry, 267(6), 3819-3824.

Vitamin C

1. Carrillo, A. E., Murphy, R. J., & Cheung, S. S. (2008). Vitamin C supplementation and salivary immune function following exercise-heat stress. International journal of sports physiology and performance, 3(4), 516-530.
2. Nakhostin-Roohi, B., Babaei, P., Rahmani-Nia, F., & Bohlooli, S. (2008). Effect of vitamin C supplementation on lipid peroxidation, muscle damage and inflammation after 30-min exercise at 75% VO^ sub 2max^. Journal of Sports Medicine and Physical Fitness, 48(2), 217.
3. Ayinde, O. C., Ogunnowo, S., & Ogedegbe, R. A. (2012). Influence of Vitamin C and Vitamin E on testicular zinc content and testicular toxicity in lead exposed albino rats. BMC Pharmacology and Toxicology, 13(1), 17.
4. Harikrishnan, R., Abhilash, P. A., Das, S. S., Prathibha, P., Rejitha, S., John, F., … & Indira, M. (2013). Protective effect of ascorbic acid against ethanol-induced reproductive toxicity in male guinea pigs. British journal of nutrition, 110(4), 689-698.
5. Jewo, P. I., Duru, F. I., Fadeyibi, I. O., Saalu, L. C., & Noronha, C. C. (2012). The protective role of ascorbic acid in burn-induced testicular damage in rats. Burns, 38(1), 113-119.
6. Saki, G., Jasemi, M., Sarkaki, A. R., & Fathollahi, A. (2013). Effect of administration of vitamins C and E on fertilization capacity of rats exposed to noise stress. Noise and Health, 15(64), 194.
7. Takhshid, M. A., Tavasuli, A. R., Heidary, Y., Keshavarz, M., & Kargar, H. (2012). Protective effect of vitamins E and C on endosulfan-induced reproductive toxicity in male rats. Iranian journal of medical sciences, 37(3), 173.
8. Karlowski, T. R., Chalmers, T. C., Frenkel, L. D., Kapikian, A. Z., Lewis, T. L., & Lynch, J. M. (1975). Ascorbic acid for the common cold: a prophylactic and therapeutic trial. Jama, 231(10), 1038-1042.

Vitamin D3

1. Pilz, S., Frisch, S., Koertke, H., Kuhn, J., Dreier, J., Obermayer-Pietsch, B., … & Zittermann, A. (2011). Effect of vitamin D supplementation on testosterone levels in men. Hormone and Metabolic Research, 43(3), 223.
2. Wehr, E., Pilz, S., Boehm, B. O., März, W., & Obermayer‐Pietsch, B. (2010). Association of vitamin D status with serum androgen levels in men.Clinical endocrinology, 73(2), 243-248.
3. Morley, J. E., Perry III, H. M., Kaiser, F. E., Kraenzle, D., Jensen, J., Houston, K., … & Perry Jr, H. M. (1993). Effects of testosterone replacement therapy in old hypogonadal males: a preliminary study. Journal of the American Geriatrics Society, 41(2), 149-152.

KSM-66® Ashwagandha

1. Raut, A. A., Rege, N. N., Tadvi, F. M., Solanki, P. V., Kene, K. R., Shirolkar, S. G., … & Vaidya, A. B. (2012). Exploratory study to evaluate tolerability, safety, and activity of Ashwagandha (Withania somnifera) in healthy volunteers. Journal of Ayurveda and integrative medicine, 3(3), 111.
2. Sandhu, J. S., Shah, B., Shenoy, S., Chauhan, S., Lavekar, G. S., & Padhi, M. M. (2010). Effects of Withania somnifera (Ashwagandha) and Terminalia arjuna (Arjuna) on physical performance and cardiorespiratory endurance in healthy young adults. International journal of Ayurveda research, 1(3), 144.
3. Ahmad, M. K., Mahdi, A. A., Shukla, K. K., Islam, N., Rajender, S., Madhukar, D., … & Ahmad, S. (2010). Withania somnifera improves semen quality by regulating reproductive hormone levels and oxidative stress in seminal plasma of infertile males. Fertility and sterility, 94(3), 989-996.
4. Gupta, A., Mahdi, A. A., Shukla, K. K., Ahmad, M. K., Bansal, N., Sankhwar, P., & Sankhwar, S. N. (2013). Efficacy of Withania somnifera on seminal plasma metabolites of infertile males: a proton NMR study at 800 MHz. Journal of ethnopharmacology, 149(1), 208-214.
5. Mahdi, A. A., Shukla, K. K., Ahmad, M. K., Rajender, S., Shankhwar, S. N., Singh, V., & Dalela, D. (2011). Withania somnifera improves semen quality in stress-related male fertility. Evidence-Based Complementary and Alternative Medicine, 2011.
6. Wankhede, S., Langade, D., Joshi, K., Sinha, S. R., & Bhattacharyya, S. (2015). Examining the effect of Withania somnifera supplementation on muscle strength and recovery: a randomized controlled trial. Journal of the International Society of Sports Nutrition, 12(1), 43.

Primavie® Purified Shilajit Extract

1. Sharma, P., Jha, J., Shrinivas, V., Dwivedi, L. K., Suresh, P., & Sinha, M. (2003). Shilajit: evalution of its effects on blood chemistry of normal human subjects. Ancient science of life, 23(2), 114.
2. Biswas, T. K., Pandit, S., Mondal, S., Biswas, S. K., Jana, U., Ghosh, T., … & Auddy, B. (2010). Clinical evaluation of spermatogenic activity of processed Shilajit in oligospermia. Andrologia, 42(1), 48-56.
3. Pandit, S., Biswas, S., Jana, U., De, R. K., Mukhopadhyay, S. C., & Biswas, T. K. (2016). Clinical evaluation of purified Shilajit on testosterone levels in healthy volunteers. Andrologia, 48(5), 570-575.

Laxopure™

1. Iglesias-Arteaga, M. A., Símuta-Lopez, E. M., Xochihua-Moreno, S., Viñas-Bravo, O., Smith, S. M., Meza Reyes, S., & Sandoval-Ramírez, J. (2005). A convenient procedure for the synthesis of 3beta-hydroxy-6-oxo-5alpha-steroids: aplication to the synthesis of laxogenin. Journal of the Brazilian Chemical Society, 16(3A), 381-385.
2. Syrov, V. N., & Kurmukov, A. G. (1975). [Experimental study of the anabolic activity of 6-ketoderivatives of certain natural sapogenins]. Farmakologiia i toksikologiia, 39(5), 631-635.
3. Esposito, D., Komarnytsky, S., Shapses, S., & Raskin, I. (2011). Anabolic effect of plant brassinosteroid. The FASEB Journal, 25(10), 3708-3719.
4. Fasciola, A. A. (2014). U.S. Patent Application No. 13/999,672.

Phosphatidylcholine

1. Hasengschwandtner, F. (2005). Phosphatidylcholine treatment to induce lipolysis. Journal of cosmetic dermatology, 4(4), 308-313.
2. Klein, S. M., Schreml, S., Nerlich, M., & Prantl, L. (2009). In vitro studies investigating the effect of subcutaneous phosphatidylcholine injections in the 3T3-L1 adipocyte model: lipolysis or lipid dissolution?. Plastic and reconstructive surgery, 124(2), 419-427.
3. Cohen, B. M., Renshaw, P. F., Stoll, A. L., Wurtman, R. J., Yurgelun-Todd, D., & Babb, S. M. (1995). Decreased brain choline uptake in older adults: an in vivo proton magnetic resonance spectroscopy study. Jama, 274(11), 902-907.
4. Ziegenfuss, T., Landis, J., & Hofheins, J. (2008). Acute supplementation with alpha-glycerylphosphorylcholine augments growth hormone response to, and peak force production during, resistance exercise. Journal of the International Society of Sports Nutrition, 5(S1), P15.

Bioperine® Black Pepper Extract

1. Shoba₁, G., Joy₁, D., Joseph₁, T., Rajendran₂, M. M. R., & Srinivas₂, P. S. S. R. (1998). Influence of piperine on the pharmacokinetics of curcumin in animals and human volunteers. Planta medica, 64, 353-356.
2. Han, H. K. (2011). The effects of black pepper on the intestinal absorption and hepatic metabolism of drugs. Expert opinion on drug metabolism & toxicology, 7(6), 721-729.
3. Bajad, S., Bedi, K. L., Singla, A. K., & Johri, R. K. (2001). Piperine inhibits gastric emptying and gastrointestinal transit in rats and mice. Planta medica, 67(02), 176-179.
4. Ononiwu, I. M., Ibeneme, C. E., & Ebong, O. O. (2002). Effects of piperine on gastric acid secretion in albino rats. African journal of medicine and medical sciences, 31(4), 293-295.

WARNING

California’s Proposition 65 entitles California consumers to special warnings.

WARNING: Cancer and Reproductive Harm - www.P65warnings.ca.gov/