When outside attackers invade the body, free radicals run rampant. Free radicals are unstable molecules that wreak havoc, damaging membranes, DNA and how cells communicate.
However, the immune system is especially vulnerable to these free radicals. Without proper antioxidant defense, the immune system is eventually overrun and can’t respond to threats.
This remarkable coenzyme’s presence in interstellar stardust has lead some scientists to believe it played a pivotal role in the evolution of life on Earth.
In fact, PQQ has been found in every plant species tested to date.
But neither humans nor the bacteria that colonize the human digestive tract are able to naturally produce it.
Which is why researchers believe PQQ should be classified as an essential nutrient.
With up to 5,000X more antioxidant power than Vitamin C, PQQ provides an unprecedented line of defense against free radicals.
Interferons are proteins essential to to a strong first line of defense. They alert the immune system that germs are in your body. More importantly, they trigger killer immune cells to fight those invaders.
Interferons got their name because they “interfere” with viruses and keep them from multiplying.
Zinc is a natural mineral found in nature that we MUST get from our diets. In fact, the body doesn’t even store zinc, so a daily supply is essential. When it comes to boosting the immune system, zinc has been shown to increase interferon levels 10-fold.
Which means that higher levels of zinc allow your immune system to recognize threats faster and stop infections before they have a chance to spread.
It’s no wonder studies have shown that zinc can decrease the duration of a cold by 5-7 days (if you think about how long a cold usually lasts, that’s almost getting rid of the cold!)
While the circulatory system works to transport oxygen and nutrients throughout the human body, the immune system protects the body by consuming foreign substances that can cause damage to the body.
Since immune cells travel via the circulatory system, poor blood flow means that fewer immune cells are available to help fight against harmful invaders.
The key to healthy circulation comes down to one thing, nitric oxide levels. Nitric oxide relaxes the inner muscles of blood vessels, causing them to widen and increase circulation.
Now, you may have heard of N.O. boosting supplements like l-arginine or citrulline, but nothing compares to the effectiveness of the amino acid glycine propionyl-l-carnitine.
Because GPLC is shown to boost nitric oxide levels by 55% in just 15 days!
It’s well proven that vitamin D levels are essential for a healthy immune system. For example…
Vitamin D levels are lowest in the winter months when cold cases are at their peak.
Vitamin D tempers the damaging inflammatory response of white blood cells, while it also boosts immune cells’ production of microbe-fighting proteins.
The best way to keep your vitamin D levels in check is through sun exposure NOT supplemental vitamin D. However, in the winter, or when you’re too sick to get off your couch, the mineral boron can help every minute of sunlight count that much more.
You see, boron allows vitamin D to stay in the blood stream longer. That’s why one study showed just 3mg of boron can help boost vitamin D levels by 39%.
Another study took place in Serbia with supplementation beginning in October and concluding by January; in other words, the study occurred during the fall transition to winter, a time when vitamin-D status would be expected to worsen. Yet, with boron supplementation, vitamin D levels rose significantly, with an average rise of 20%.
Mitochondria produce the energy that every single cell in your body needs to survive. Muscle cells, heart cells, brain cells, and immune cells … they all rely on your mitochondria to operate efficiently. Which is why the mitochondria are often refered to as the “powerplants” of the cell.
Immune cells use the energy from the mitochondria to respond to threats. Without this energy, “defender” cells don’t have the juice to do their job.
L-carnitine transports fatty acids into the mitochondria so they can be turned into fuel for every cell in the body.
Simply put, L- carnitine is pipeline between your mitochondria and the rest of your body.
ALCAR is the the only form of carnitine that can easily pass through the blood brain barrier to keep your neurons and other brain cells working safe from infections.
Research also shows it can help reduce stress, improve mood, and help give you a jolt of mental energy.
A viral infection occurs when the body is invaded by pathogenic viruses, and infectious virus particles attach to and enter susceptible cells
Shilajit is a natural, tar-like substance that’s found only in the upper reaches of the Himalayan mountains. Its known by the locals as the “conqueror of mountains” and the “destroyer of weakness” because of its potent effects on male immunity.
Plus, its remarkable ability to give the local Sherpas the almost supernatural strength and stamina they need to scale Mount Everest.
Most importantly, shilajit is shown to be a potent antiviral, providing essential immune support.
Other Ingredients: Natural Flavors, Erythritol, Citric Acid, Steviol Glycosides(95%), Beet Root Juice Powder, Silicon Dioxide.
Even though modern medicine and technology allows us to live longer than ever – we are not living better. The extra decades we’ve gained are plagued with diseases of the body and mind. What good is living to 100 if you spend the last 20 years of your life in a nursing home, bed ridden, and in constant pain?
How can living for over a century be considered a “success” if you can’t even remember the names and faces of your loved ones? That’s why we created Ouro Vitae: to help you live healthier, for longer. We never want you to look back and think, ” those were the best years of my life”.
Using both the latest innovations in science and the most time-tested remedies, we want to make every year better than the last.
My name is Peter Monsen and I’m the Chief Science Officer at Ouro Vitae.
I spent the last few decades researching nutrition and teaching biochemistry at a top research university ….While helping my family run an elite fitness and training gym on Long Island, New York.
We trained dozens of NFL, NHL, MLB and MMA athletes at our facility … As well as many topflight medical and Wall Street professionals.
Helping them maintain the energy, strength and stamina they had in their youth … So they could continue to compete at the highest level.
I can honestly say I’ve spent the bulk of my life dedicated to researching peak performance …
And more, specifically, how to maintain this peak performance well into old age.
Because you’re covered by our 30-day 100% money-back guarantee.
It’s important to us that money doesn’t come between you and the solution your energy and health craves.
So we want to make this easy.
If for any reason you don’t get the results, we’ve expressed over the trial period …
Simply return your EMPTY bottles of Mito Male for a FULL, no-questions-asked refund.
Because the reality is:
If somehow Mito Male fails to deliver the results we promise…
We don’t want to keep a penny of YOUR money.
Yes! Mito Male was designed to be taken daily to achieve the desired benefits. This formula can be taken with or without food. Our staff loves sipping on a glass in the morning to start our days off right and set the tone to dominate life.
You can also mix it with any liquid of your liking, including adding it to smoothies and shakes for a vitality enhancement cocktail unlike any other.
Men over 40 years old is where you see the biggest drop off in Vitality, but Mito Male can still provide younger men with a plethora of benefits like the energy and focus boosting effects of acetyl L carnitine…athletic enhancement from glycine propionyl-l-carnitine…fatigue fighting power of shilajit…antioxident supercharging of PQQ,… and the hormone assistance you get from boron and zinc.
We believe in 100% transparency with all our products. We want you to know exactly how much of each ingredient is in our formula so you know you’re getting the proper doses, backed by science.
Ouro Vitae refuses to hide behind the “proprietary blends” so prevalent in the supplement industry.
Because this allows a company to load a laundry list of ingredients in their formula, making it look remarkable.
But on the inside, “proprietary blends” can have such small amounts of an ingredient it’s absolutely useless to you. Meaning, they’re marketable, but not remarkable.
Simply put, the ingredients in Mito Male are all available without a RX , and that means the big pharma companies can’t make a penny off them so they’re not marketed to hospitals.
Instead, they can charge over $500 a month for HRT which usually comes with painful procedures, constant blood draws and monitoring, and tons of doctor visits.
Absolutely not. Mito Male is free from artificial sweeteners and coloring.
Ouro Vitae, 2137 Mystic Cove Drive Virginia Beach VA 23455
*These statements have not been evaluated by the Food and Drug Administration. Our products are not intended to diagnose, treat, cure or prevent any disease.
© 2018 Ouro Vitae. All rights reserved.
The information provided on this site is for informational purposes only and is not intended as a substitute for advice from your physician or other health care professional or any information contained on or in any product label or packaging. You should not use the information on this site for diagnosis or treatment of any health problem or for prescription of any medication or other treatment. None of our statements or information, including health claims, articles, advertising or product information have been evaluated or approved by the United States Food and Drug Administration (FDA). The products or ingredients referred to on this site are not intended to diagnose, treat, cure or prevent any disease. You should consult with a healthcare professional before starting any diet, exercise or supplementation program, before taking any medication, or if you have or suspect you might have a health problem.
1. Cavallini, G., Caracciolo, S., Vitali, G., Modenini, F., & Biagiotti, G. (2004). Carnitine versus androgen administration in the treatment of sexual dysfunction, depressed mood, and fatigue associated with male aging. Urology, 63(4), 641-646. doi:10.1016/j.urology.2003.11.009
2. Malaguarnera, M., Cammalleri, L., Gargante, M. P., Vacante, M., Colonna, V., & Motta, M. (2007). L-Carnitine treatment reduces severity of physical and mental fatigue and increases cognitive functions in centenarians: A randomized and controlled clinical trial. The American Journal of Clinical Nutrition, 86(6), 1738-1744. doi:10.1093/ajcn/86.5.1738
3. Karlic, H., & Lohninger, A. (2004). Supplementation of l-carnitine in athletes: Does it make sense? Nutrition, 20(7-8), 709-715. doi:10.1016/j.nut.2004.04.003
4. Samimi, M., Jamilian, M., Ebrahimi, F. A., Rahimi, M., Tajbakhsh, B., & Asemi, Z. (2016). Oral carnitine supplementation reduces body weight and insulin resistance in women with polycystic ovary syndrome: A randomized, double-blind, placebo-controlled trial. Clinical Endocrinology,84(6), 851-857. doi:10.1111/cen.13003
5. Sahlin, K. (2011). Boosting fat burning with carnitine: An old friend comes out from the shadow. The Journal of Physiology, 589(7), 1509-1510. doi:10.1113/jphysiol.2011.205815
6. Soczynska, J. K., Kennedy, S. H., Chow, C. S., Woldeyohannes, H. O., Konarski, J. Z., & Mcintyre, R. S. (2008). Acetyl-L-carnitine and α-lipoic acid: Possible neurotherapeutic agents for mood disorders? Expert Opinion on Investigational Drugs, 17(6), 827-843. doi:10.1517/135437184.108.40.2067
7. Miyagawa, T., Kawamura, H., Obuchi, M., Ikesaki, A., Ozaki, A., Tokunaga, K., . . . Honda, M. (2013). Effects of Oral L-Carnitine Administration in Narcolepsy Patients: A Randomized, Double-Blind, Cross-Over and Placebo-Controlled Trial. PLoS ONE,8(1). doi:10.1371/journal.pone.0053707
8. Cristofano, A., Sapere, N., Marca, G. L., Angiolillo, A., Vitale, M., Corbi, G., . . . Costanzo, A. D. (2016). Serum Levels of Acyl-Carnitines along the Continuum from Normal to Alzheimers Dementia. Plos One, 11(5). doi:10.1371/journal.pone.0155694
. Fillit, H., & Hill, J. (2004). The Economic Benefits of Acetylcholinesterase Inhibitors for Patients with Alzheimer Disease and Associated Dementias. Alzheimer Disease & Associated Disorders,18. doi:10.1097/01.wad.0000127492.65032.d3
10. Miyata, M., Yoshihisa, A., Yamauchi, H., Owada, T., Sato, T., Suzuki, S., . . . Takeishi, Y. (2014). Impact of sleep-disordered breathing on myocardial damage and metabolism in patients with chronic heart failure. Heart and Vessels, 30(3), 318-324. doi:10.1007/s00380-014-0479-6
11. Lango, R. (2001). Influence of ?-carnitine and its derivatives on myocardial metabolism and function in ischemic heart disease and during cardiopulmonary bypass. Cardiovascular Research, 51(1), 21-29. doi:10.1016/s0008-6363(01)00313-3
12. Vescovo, G., Ravara, B., Gobbo, V., Sandri, M., Angelini, A., Barbera, M. D., . . . Libera, L. D. (2002). L-Carnitine: A potential treatment for blocking apoptosis and preventing skeletal muscle myopathy in heart failure. American Journal of Physiology-Cell Physiology, 283(3). doi:10.1152/ajpcell.00046.2002
13. Shadboorestan, A., Shokrzadeh, M., Ahangar, N., Abdollahi, M., Omidi, M., & Payam, S. S. (2013). The chemoprotective effects of l-carnitine against genotoxicity induced by diazinon in rat blood lymphocyte. Toxicology and Industrial Health,31(12), 1334-1340. doi:10.1177/0748233713491811
14. Chowanadisai, W., Bauerly, K. A., Tchaparian, E., Wong, A., Cortopassi, G. A., & Rucker, R. B. (2009). Pyrroloquinoline Quinone Stimulates Mitochondrial Biogenesis through cAMP Response Element-binding Protein Phosphorylation and Increased PGC-1α Expression. Journal of Biological Chemistry,285(1), 142-152. doi:10.1074/jbc.m109.030130
15. Chowanadisai, W., Bauerly, K. A., Tchaparian, E., Wong, A., Cortopassi, G. A., & Rucker, R. B. (2009). Pyrroloquinoline Quinone Stimulates Mitochondrial Biogenesis through cAMP Response Element-binding Protein Phosphorylation and Increased PGC-1α Expression. Journal of Biological Chemistry, 285(1), 142-152. doi:10.1074/jbc.m109.030130
16. Stites TE, Mitchell AE, Rucker RB. Physiological importance of quinoenzymes and the O-quinone family of cofactors. J Nutr. 2000 Apr;130(4):719-27
17. Steinberg, F., Stites, T. E., Anderson, P., Storms, D., Chan, I., Eghbali, S., & Rucker, R. (2003). Pyrroloquinoline Quinone Improves Growth and Reproductive Performance in Mice Fed Chemically Defined Diets. Experimental Biology and Medicine, 228(2), 160-166. doi:10.1177/153537020322800205
18. 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. doi:10.1111/j.1439-0272.2009.00956.x
19. Surapaneni, D. K., Adapa, S. R., Preeti, K., Teja, G. R., Veeraragavan, M., & Krishnamurthy, S. (2012). Shilajit attenuates behavioral symptoms of chronic fatigue syndrome by modulating the hypothalamic–pituitary–adrenal axis and mitochondrial bioenergetics in rats. Journal of Ethnopharmacology, 143(1), 91-99. doi:10.1016/j.jep.2012.06.002
20. Chang, C. S., Choi, J. B., Kim, H. J., & Park, S. B. (2011). Correlation Between Serum Testosterone Level and Concentrations of Copper and Zinc in Hair Tissue. Biological Trace Element Research,144(1-3), 264-271. doi:10.1007/s12011-011-9085-y
21. Plasma Steroid-Binding Proteins in Tumour Diseases. (1984). Molecular Aspects of Medicine, 371-380. doi:10.1016/b978-0-08-033239-0.50032-6
1. Dai YL, Luk TH, Yiu KH, et al. Reversal of mitochondrial dysfunction by coenzyme Q10 supplement improves endothelial function in patients with ischaemic left ventricular systolic dysfunction: a randomized controlled trial. Atherosclerosis. 2011 Jun;216(2):395-401.
2. Mehrabani, S., Askari, G., Miraghajani, M., Tavakoly, R., & Arab, A. (2019). Effect of coenzyme Q10 supplementation on fatigue: A systematic review of interventional studies. Complementary Therapies in Medicine, 43, 181–187. doi: 10.1016/j.ctim.2019.01.022
3. Dumont, M., Kipiani, K., Yu, F., Wille, E., Katz, M., Calingasan, N. Y., … Beal, M. F. (2011). Coenzyme Q10 Decreases Amyloid Pathology and Improves Behavior in a Transgenic Mouse Model of Alzheimers Disease. Journal of Alzheimers Disease, 27(1), 211–223. doi: 10.3233/jad-2011-110209
4. Mezawa M, Takemoto M, Onishi S, et al. The reduced form of coenzyme Q10 improves glycemic control in patients with type 2 diabetes: An open label pilot study. Biofactors. 2012 Aug 8.
5. Hernández-Camacho, J. D., Bernier, M., López-Lluch, G., & Navas, P. (2018). Coenzyme Q10 Supplementation in Aging and Disease. Frontiers in Physiology, 9. doi: 10.3389/fphys.2018.00044
6. Crowley D.C., et al. “Bioavailability and Health Effects of CoQ10 in Healthy Human Adults.” May 11, 2006.
7. Kalén, A., Appelkvist, E.-L., & Dallner, G. (1989). Age-related changes in the lipid compositions of rat and human tissues. Lipids, 24(7), 579–584. doi: 10.1007/bf02535072
8. Effects of carnitine and coenzyme Q10 on lipid profile and serum levels of lipoprotein(a) in maintenance hemodialysis patients on statin therapy. (2011). Iranian Journal of Kidney Diseases. doi: 21368390
9. Vargiu, R., Littarru, G. P., Faa, G., & Mancinelli, R. (2008). Positive inotropic effect of coenzyme Q10, omega-3 fatty acids and propionyl-L-carnitine on papillary muscle force-frequency responses of BIO TO-2 cardiomyopathic Syrian hamsters. BioFactors, 32(1-4), 135–144. doi: 10.1002/biof.5520320116
10. Johansson, P., Dahlström, Ö., Dahlström, U., & Alehagen, U. (2015). Improved health-related quality of life, and more days out of hospital with supplementation with selenium and coenzyme Q10 combined. Results from a double blind, placebo-controlled prospective study. The Journal of Nutrition, Health & Aging, 19(9), 870–877. doi: 10.1007/s12603-015-0509-9
11. Adarsh, K., Kaur, H., & Mohan, V. (2008). Coenzyme Q10(CoQ10) in isolated diastolic heart failure in hypertrophic cardiomyopathy (HCM). BioFactors, 32(1-4), 145–149. doi: 10.1002/biof.5520320117
12. Burke, B. E., Neuenschwander, R., & Olson, R. D. (2001). Randomized, Double-Blind, Placebo- Controlled Trial of Coenzyme Q10 in Isolated Systolic Hypertension. Southern Medical Journal, 94(11), 1112–1117. doi: 10.1097/00007611-200111000-00015
13. Zhai, J., Bo, Y., Lu, Y., Liu, C., & Zhang, L. (2017). Effects of Coenzyme Q10 on Markers of Inflammation: A Systematic Review and Meta-Analysis. Plos One, 12(1). doi: 10.1371/journal.pone.0170172
14. Lewin, A., & Lavon, H. (1997). The effect of coenzyme Q10 on sperm motility and function. Molecular Aspects of Medicine, 18, 213–219. doi: 10.1016/s0098-2997(97)00036-8
15. Preethi Srikanthan, Arun S. Karlamangla. Muscle Mass Index as a Predictor of Longevity in Older-Adults. The American Journal of Medicine, 2014; DOI: 10.1016/j.amjmed.2014.02.007
16. Folkers, K., & Simonsen, R. (1995). Two successful double-blind trials with coenzyme Q10 (vitamin Q10) on muscular dystrophies and neurogenic atrophies. Biochimica Et Biophysica Acta (BBA) – Molecular Basis of Disease, 1271(1), 281–286. doi: 10.1016/0925-4439(95)00040-b
17. Farsi, F., Mohammadshahi, M., Alavinejad, P., Rezazadeh, A., Zarei, M., & Engali, K. A. (2015). Functions of Coenzyme Q10 Supplementation on Liver Enzymes, Markers of Systemic Inflammation, and Adipokines in Patients Affected by Nonalcoholic Fatty Liver Disease: A Double-Blind, Placebo-Controlled, Randomized Clinical Trial. Journal of the American College of Nutrition, 35(4), 346–353. doi: 10.1080/07315724.2015.1021057