The brain is also affected by this sexual differentiation;[13] the enzyme aromatase converts testosterone into estradiol that is responsible for masculinization of the brain in male mice. In humans, masculinization of the fetal brain appears, by observation of gender preference in patients with congenital diseases of androgen formation or androgen receptor function, to be associated with functional androgen receptors.[95]

In summary it’s important to know that this topic is still hotly debated, and there are a lot of inconsistencies in the data. We do know that soy contains phytoestrogens and does seem to have a lot of affects on the body, including some studies that show decreased Testosterone levels. For that reason (and the fact that it tastes like ass) I avoid it, and I recommend you also avoid it (in particular soy isolates!) if you’re seeking higher testosterone.
In a placebo-controlled study, 27 Division II football players received either a placebo or a ZMA supplement for a total of seven weeks during their scheduled spring practice. At the end of the seven weeks, the players taking the ZMA supplement had a 30 percent increase in testosterone, while the placebo group had a 10 percent decrease. The ZMA group also saw an 11.6 percent increase in strength, compared to only 4.6 percent in the placebo group.[7]
You can search every supplement on the market, and you can try reading “how to be good at sex” books (there’s about a million of them); You can even try those strange penis exercises (please do not waste your time). Or you can take a daily supplement that is designed and developed to do one thing: transform your penis and sex life so the next time a girl is talking about some guy who “could not stop making me orgasm,” that guy is you!
A little goes a long way for men, but clinically many men do well with 5 to 10 mg of a topical progesterone cream at bedtime, again, only under your doctor’s supervision. Arginine is important for nitric oxide (NO) production and should be taken twice daily. I've also been recommending Testoplex™ for years. It's Xymogen’s formulation—featuring mungbean sprout powder—to address healthy testosterone levels and provide support for libido and overall vitality.
Both testosterone and 5α-DHT are metabolized mainly in the liver.[1][151] Approximately 50% of testosterone is metabolized via conjugation into testosterone glucuronide and to a lesser extent testosterone sulfate by glucuronosyltransferases and sulfotransferases, respectively.[1] An additional 40% of testosterone is metabolized in equal proportions into the 17-ketosteroids androsterone and etiocholanolone via the combined actions of 5α- and 5β-reductases, 3α-hydroxysteroid dehydrogenase, and 17β-HSD, in that order.[1][151][152] Androsterone and etiocholanolone are then glucuronidated and to a lesser extent sulfated similarly to testosterone.[1][151] The conjugates of testosterone and its hepatic metabolites are released from the liver into circulation and excreted in the urine and bile.[1][151][152] Only a small fraction (2%) of testosterone is excreted unchanged in the urine.[151]
Rumor has it that the Kim sisters' testosterone pill received a reaction that no other product has ever gotten on Shark Tank. Apparently, after watching a presentation from the pair and hearing about how well their product has performed so far, all five judges got into a heated argument over who would make a deal with the two young entrepreneurs. It's been said that the fight lasted nearly an hour before the judges decided to do something that's never been done before. All five Sharks teamed up to invest an unbelievable $2.5 million into the Kim sisters' product!

A: Androderm comes in the form of a transdermal patch and is used for testosterone replacement therapy in patients who have insufficient levels of testosterone. Testosterone is a hormone produced in the body that plays a key role in many physiological processes in men. In some men, however, the body does not produce enough of the hormone, resulting in a variety of symptoms including decreased libido, erectile dysfunction, muscle loss, anemia and depression, among others. Androderm helps treat these symptoms and raise low testosterone levels by delivering therapeutic amounts of the hormone, which are absorbed through the skin. According to the prescribing information for Androderm, depression was a reported side effect of the medication. Other common side effects of Androderm include itching and redness at the application site, prostate abnormalities, headache, and burning or hardening of the skin at the application site. Less common side effects of Androderm include reduced libido (sex drive), fatigue, high blood pressure, anxiety, confusion, increased appetite, and body pain. For more specific information, consult with your doctor for guidance based on your health status and current medications, particularly before taking any action. Your physician can determine if your dosage of the medication needs to be adjusted or if an alternative medication should be considered. Lori Poulin, PharmD
Zinc deficiency also negatively affects testosterone levels, according a 2014 article in the Journal of Plant Biochemistry and Physiology. The authors of this review note that zinc supplementation can increase circulating testosterone in some populations. In fact, daily supplementation with typical doses may double testosterone within a few months.

While it would be nice to buy a testosterone pill from the local supplement store and have your testosterone levels go up, such a magic pill does not exist. As you can see from the above rundown, while a few supplements may be somewhat effective if your T levels are already low, none will significantly raise your testosterone above a baseline level. Thus, the basics of keeping your T levels high remain pretty simple:

$(function(){ SocialButtonRound_OnLoad(); }); function OpenPopup(a, b, c, d, e, f) { var g, h, i, j, k, l = ""; if (1 == e) if ("REST" == f.toUpperCase() ? (j = rest_width, k = rest_height) : (j = onet_width, k = onet_height), navigator.userAgent.toUpperCase().indexOf("OPERA") == -1 && navigator.userAgent.toUpperCase().indexOf("MAC") == -1 || (k += 15), document.all) { var m = "no"; d && (m = "yes"), h = 0, i = 0, j = screen.width, k = screen.height; var n = "fullscreen=yes"; g =, l, n) } else { j += 20, h = 0, i = 0, j = screen.width, k = screen.height; var n = "fullscreen=yes"; g =, l, n) } else if (document.all) { var m = "no"; d && (m = "yes"), h = (screen.width - b) / 2, i = (screen.height - c) / 2; var n = "left=" + h + ",top=" + i + ",width=" + b + ",height=" + c + ",menu=no,address=no,resize=no,scrollbars=" + m + ",titlebar=no,status=no"; g =, l, n) } else { b += 20, h = (screen.width - b) / 2, i = (screen.height - c) / 2; var n = "left=" + h + ",top=" + i + ",width=" + b + ",height=" + c + ",menu=no,address=no,resize=no,status=no"; g =, l, n) } return g } function SocialButtonRound_OnLoad() { try { addLinksToShareIcon(), generateShareCount(document.location.href), $(" > li > a").not("a.mailtolink").click(function (a) { a.preventDefault(), etafScrollPos = $(document).scrollTop(), window._vis_opt_queue = window._vis_opt_queue || [], window._vis_opt_queue.push(function () { _vis_opt_goal_conversion(243) }); var b = $(this).parent("li").attr("data-social-btn"), c = $(this).attr("href"); switch (b) { case "facebook": OpenPopup(c, 670, 340, !1, 0, ""); break; case "print": window.print(); break; case "chat": break; default: console.log("Unsupported data-social-btn type: " + b) } return !1 }) } catch (a) { } } function addLinksToShareIcon() { var a = window.location, a.indexOf("?") >= 0 && (a = a.substring(0, a.indexOf("?"))); a.indexOf("#") >= 0 && (a = a.substring(0, a.indexOf("#"))); $(' > li[data-social-btn="facebook"] > a').attr("href", "" + encodeURIComponent(a)); } function generateShareCount(a) { a.indexOf("?") >= 0 && (a = a.substring(0, a.indexOf("?"))); a.indexOf("#") >= 0 && (a = a.substring(0, a.indexOf("#"))); if (a.indexOf("https://") > -1) { var b = encodeURIComponent(a); getFBCount(b) }; } function getFBCount(a) { $.ajax({ url: "" + a, dataType: "jsonp", success: function (a) { a.share && ($("#shareCountContainer").val(Number($("#shareCountContainer").val()) + Number(a.share.share_count)), addToShareCountAndUpdate()) } }) } function addToShareCountAndUpdate() { if (!isNaN($("#shareCountContainer").val())) { var a = Number($("#shareCountContainer").val()); a >= 1e3 && (a = parseFloat((a / 1e3).toFixed(1)) + "K"), $("span[data-share-counter]").html(a) } }
Estrogen is important in men, but too high of a level has all sorts of negative consequences – ranging from heart attacks to prostate cancer (32 & 33). The balance between testosterone and estrogen (or estradiol) is critical for a man. If the ratio is out and estrogen starts to dominate you run into all sorts of issues – such as breast cell growth, prostate enlargement and of course lower testosterone.
That said, magnesium is one of a few ingredients demonstrated to impact testosterone levels. Researchers at Italy’s University of Palermo found that magnesium improved participants’ anabolic hormone status — including their testosterone levels. In a follow-up study, they confirm that even adjusting for age differences in their participant group, “magnesium was positively associated with total testosterone.” They propose that magnesium supplementation might help improve muscle performance in aging men — a group particularly vulnerable to declining/low testosterone levels. Outside of Italy, researchers at Turkey’s Selçuk University found that magnesium supplementation increased testosterone levels for both athletes and more sedentary men alike.
Thus, alcohol metabolism destroys the essential coenzyme required for T synthesis. Alcohol also contributes to the release of special endorphins which inhibit hormone production. In addition, drinking too much alcohol leads to the elevation of estrogen levels in men because of the conversion of testosterone in estrogen. It means that T levels come down with a run.
Findings that improvements in serum glucose, serum insulin, insulin resistance or glycemic control, in men treated with testosterone are accompanied by reduced measures of central obesity, are in line with other studies showing a specific effect of testosterone in reducing central or visceral obesity (Rebuffe-Scrive et al 1991; Marin, Holmang et al 1992). Furthermore, studies that have shown neutral effects of testosterone on glucose metabolism have not measured (Corrales et al 2004), or shown neutral effects (Lee et al 2005) (Tripathy et al 1998; Bhasin et al 2005) on central obesity. Given the known association of visceral obesity with insulin resistance, it is possible that testosterone treatment of hypogonadal men acts to improve insulin resistance and diabetes through an effect in reducing central obesity. This effect can be explained by the action of testosterone in inhibiting lipoprotein lipase and thereby reducing triglyceride uptake into adipocytes (Sorva et al 1988), an action which seems to occur preferentially in visceral fat (Marin et al 1995; Marin et al 1996). Visceral fat is thought to be more responsive to hormonal changes due to a greater concentration of androgen receptors and increased vascularity compared with subcutaneous fat (Bjorntorp 1996). Further explanation of the links between hypogonadism and obesity is offered by the hypogonadal-obesity-adipocytokine cycle hypothesis (see Figure 1). In this model, increases in body fat lead to increases in aromatase levels, in addition to insulin resistance, adverse lipid profiles and increased leptin levels. Increased action of aromatase in metabolizing testosterone to estrogen, reduces testosterone levels which induces further accumulation of visceral fat. Higher leptin levels and possibly other factors, act at the pituitary to suppress gonadotrophin release and exacerbate hypogonadism (Cohen 1999; Kapoor et al 2005). Leptin has also been shown to reduce testosterone secretion from rodent testes in vitro (Tena-Sempere et al 1999). A full review of the relationship between testosterone, insulin resistance and diabetes can be found elsewhere (Kapoor et al 2005; Jones 2007).
Testosterone levels generally peak during adolescence and early adulthood. As you get older, your testosterone level gradually declines — typically about 1 percent a year after age 30 or 40. It is important to determine in older men if a low testosterone level is simply due to the decline of normal aging or if it is due to a disease (hypogonadism).