Beyond ED: How tadalafil (Cialis) may help fight belly fat, protect bones, and even combat prostate cancer

Seagal

Well-Known Member

Tadalafil and Adipose Tissue: Clinical and Preclinical Observations
Serendipity, a clinical observation coming from our pilot study, suggested that the administration of tadalafil in men with ED was associated with an increase of the serum testosterone/estradiol (T/E2) ratio, mainly due to a significant reduction of E2 levels [4]. In that pilot study, where both lean and obese subjects were investigated, no clear-cut explanation for the observed serum E2 decrease was found or why this effect might have occurred. Even if a possible variation of the ARO activity was hypothesized, in that moment, any potential effects of PDE5i on ARO were unexplored. So, on the basis of our previous pilot study, we successively investigated the potential role of chronic tadalafil administration in men affected by ED and metabolic disorders, and we demonstrated its ability to improve insulin secretion and reduce visceral fat mass [10]. Similar observations have been reported by other published clinical studies [13] and by clinical trials actually registered on ClinicalTrials.gov which investigate the possible role of tadalafil on metabolism and body composition disorders (Table 1). Importantly, successive preclinical studies confirmed our clinical observation in men [9,14]. In a mouse model of diet-induced, insulin-resistant, chronic treatment with the PDE5i sildenafil caused a significant improvement in insulin sensitivity [14]. This result was promptly investigated in a successive animal study by controlling the expression and activity of PDE5 in different cell lines of rabbit adipose tissue (i.e., visceral vs. subcutaneous) in different metabolic conditions. This study demonstrated that tadalafil counteracted high fat, diet-associated visceral adipose tissue alterations by restoring insulin sensitivity and prompting preadipocytes differentiation towards a metabolically healthy phenotype where brown, fat-specific genes (such as uncoupling protein-1) are mostly expressed [9]. Apart from clinical and preclinical observations, controversial data confirming a role for PDE5 in adipocyte biology in vitro have been reported [3]. On the basis of our previous clinical observations, as confirmed by successive preclinical data, we subsequently found for the first time that PDE5 mRNA is present in human adipocytes and that selective PDE5 inhibition significantly stimulated ARO mRNA expression in mature adipocytes in vitro upon short-time exposure with a parallel increase in E2 concentrations in the supernatant [3]. E2 is synthesized by cytochrome P450-ARO, which converts androgens into estrogens; indeed, changes at the level of estrogen biosynthesis are closely related to modifications in the transcription of ARO and may exert an important role in the prevention of cardiovascular and metabolic disease [3]. These findings showed, for the first time, that acute PDE5 inhibition was able to increase ARO mRNA expression, which should reflect positive, anti-adipogenic effects. Finally, another study confirmed that even human skeletal muscle cells are a target tissue of tadalafil, and experimental data support its pharmacological actions on modulating glucose metabolism through a direct control on insulin signaling, on improving sex hormones profile and body composition, and on ARO expression, as well as on increasing exercise capacity due to its cardiovascular and vasodilatory effects, as demonstrated by in vitro and in vivo studies [12]. However, to date, neither the molecular mechanisms underlining the interactions between tadalafil, steroid hormones and skeletal muscle metabolism and differentiation are clear, nor are the mechanisms by which PDE5i might positively influence hormone metabolism and physical activity. These clinical and preclinical results led us to conclude that, at least in theory, a dose-dependent, tadalafil-related stimulation of ARO activity could positively modulate the serum T/E2 ratio in vivo during chronic treatment with tadalafil, and this might represent a possible mechanism influencing fat-mass content and its hormonal functions [3]. Thus, we can speculate that the stimulation of the NO/cGMP signal transduction system through a PDE5 blockade can provide a new, effective and reliable ‘target’ for deranged adipose tissue pathways, suggesting its potential role in the treatment of some forms of abdominal fat accumulation and mild obesity (Figure 1).
 
Thanks for the interesting info @Seagal !

In lay language:

How Tadalafil (Cialis) May Help with Body Fat and Metabolism​


The Discovery​


Researchers stumbled upon something unexpected while studying tadalafil (the active ingredient in Cialis) for erectile dysfunction. Men taking it showed a healthier balance between testosterone and estrogen—mainly because their estrogen levels dropped. This was surprising, and they wanted to understand why.


What the Research Found​


In clinical studies with men:


  • Tadalafil improved how the body handles insulin (the hormone that controls blood sugar)
  • It reduced belly fat (visceral fat—the dangerous fat around your organs)
  • These benefits were seen in men with both ED and metabolic problems

In animal studies:


  • Mice on high-fat diets became more sensitive to insulin when given a similar medication
  • In rabbits, tadalafil helped convert unhealthy fat cells into healthier ones that actually burn energy (similar to "brown fat," which generates heat rather than storing calories)

In lab studies with human cells:


  • Fat cells exposed to tadalafil showed increased activity of aromatase—an enzyme that converts testosterone to estrogen
  • Muscle cells also responded to tadalafil, showing improvements in how they process glucose and respond to insulin

Why This Matters​


The researchers believe tadalafil works by boosting a signaling pathway in fat tissue (called NO/cGMP). This appears to help:


  • Improve insulin sensitivity
  • Encourage fat cells to behave in healthier ways
  • Potentially reduce belly fat accumulation

The Bottom Line​


While tadalafil is primarily used for erectile dysfunction, this research suggests it may have additional benefits for men struggling with metabolic issues and excess abdominal fat. The medication might offer a way to target unhealthy fat tissue directly, though more research is needed to fully understand how this works.
 

Beyond the Bedroom: The Surprising Science of Tadalafil​

How a common erectile dysfunction medication may help fight belly fat, protect bones, and even combat prostate cancer

When most people hear the word tadalafil (better known by its brand name Cialis), they think of one thing: treating erectile dysfunction. And while that remains its primary use, scientists have discovered something remarkable—this medication appears to have far-reaching effects throughout the body that could revolutionize how we approach obesity, osteoporosis, and even cancer treatment.

A comprehensive 2022 review published in the International Journal of Molecular Sciences brings together years of research revealing that tadalafil does much more than improve blood flow to one particular area. The findings suggest this well-established medication could become a valuable tool in fighting some of the most common health challenges facing aging adults.

Understanding the Science: What Tadalafil Actually Does​

To appreciate why tadalafil might help with such diverse conditions, it helps to understand its basic mechanism. Tadalafil belongs to a class of drugs called PDE5 inhibitors. PDE5 (phosphodiesterase type 5) is an enzyme found throughout your body that breaks down a signaling molecule called cGMP. When cGMP accumulates, it causes blood vessels to relax and widen, improving blood flow.

Here's the key insight: while PDE5 is most abundant in the genital area (which is why the drug works for erectile dysfunction), this enzyme exists in many other tissues—including fat cells, bone cells, and prostate tissue. This widespread distribution means that when you take tadalafil, you're not just affecting one part of your body; you're influencing cellular processes in multiple organ systems.

But the story gets even more interesting. Recent research has revealed that tadalafil doesn't just work through PDE5 inhibition. It also appears to directly affect how cells process sex hormones like testosterone and estrogen, potentially explaining its wide-ranging effects.

Fighting the Dangerous Fat: Tadalafil and Visceral Obesity​

Not all body fat is created equal. The fat that accumulates around your internal organs—called visceral fat—is particularly dangerous. Unlike the fat just beneath your skin, visceral fat actively secretes hormones and inflammatory compounds that increase your risk of heart disease, type 2 diabetes, and metabolic syndrome. It's the fat that gives some people an "apple-shaped" body, and it's notoriously difficult to lose.

The discovery that tadalafil might help came almost by accident. Researchers conducting a pilot study on men with erectile dysfunction noticed something unexpected: those taking tadalafil showed changes in their hormone levels. Specifically, they had lower estrogen levels and a higher testosterone-to-estrogen ratio. Since fat cells produce estrogen through an enzyme called aromatase, this finding hinted that tadalafil might be affecting fat metabolism.

Follow-up studies confirmed these observations. In men with erectile dysfunction and metabolic disorders, chronic tadalafil treatment improved insulin secretion and reduced visceral fat mass. Animal studies provided further support: mice fed a high-fat diet and treated with PDE5 inhibitors showed significant improvements in insulin sensitivity.

The mechanism appears to work like this: tadalafil affects fat cell development, encouraging immature fat cells (preadipocytes) to develop into a healthier type of fat tissue. Laboratory studies showed that treated fat cells expressed more "brown fat" genes—the metabolically active type of fat that burns calories rather than storing them. This shift could help explain why the drug reduces harmful visceral fat accumulation.

Several clinical trials listed on ClinicalTrials.gov have investigated these effects, examining outcomes including body weight, BMI, waist circumference, body fat percentage, and cholesterol levels. The consistency of positive findings across multiple studies suggests this isn't a fluke but rather a genuine therapeutic effect worthy of further exploration.

Building Stronger Bones: A New Approach to Osteoporosis​

Osteoporosis—the progressive weakening of bones that affects millions of older adults—has proven stubbornly difficult to treat. Current medications can slow bone loss or modestly increase bone density, but the search continues for better options. Emerging research suggests tadalafil might offer unexpected benefits for bone health.

The connection between PDE5 and bone isn't obvious at first, but scientists have known for decades that nitric oxide (NO)—the molecule that triggers the pathway tadalafil enhances—plays an important role in bone health. Mice lacking the ability to produce NO develop osteoporosis-like bone loss, while drugs that boost NO signaling improve bone mineral density and reduce fracture risk.

A particularly compelling study found that PDE5 expression increases in the bones of aging mice compared to younger animals. This suggests that as we age, our bones may become less responsive to the beneficial effects of NO signaling—and that blocking PDE5 could help restore this protective mechanism.

When researchers treated mice with tadalafil or vardenafil (another PDE5 inhibitor), they observed increased bone mass. The drugs appeared to work through multiple mechanisms: directly stimulating bone-building cells (osteoblasts), enhancing blood vessel formation within bone tissue, and modulating genes involved in bone formation. Perhaps most intriguingly, the drugs also affected neurons that connect to bone tissue, suppressing signals that normally inhibit bone formation.

Laboratory studies on human bone cells (osteoblasts) revealed another mechanism: tadalafil increased androgen receptor expression while decreasing aromatase activity. In practical terms, this means the drug may help bone cells respond better to testosterone while reducing the conversion of testosterone to estrogen. This hormonal shift could favor bone building over bone breakdown.

The implications are significant. Nearly half of men over 50 have osteopenia (reduced bone density), and the researchers suggest that men already taking PDE5 inhibitors for erectile dysfunction or urinary symptoms may be inadvertently protecting their bones. However, they caution that dedicated clinical trials focusing on bone outcomes are needed before tadalafil can be recommended specifically for osteoporosis prevention.

A Potential Cancer Fighter: Tadalafil and Prostate Cancer​

Perhaps the most intriguing—and potentially most important—findings involve prostate cancer. This is particularly relevant because PDE5 inhibitors are commonly prescribed to men with benign prostate enlargement (BPH), and are often used for sexual rehabilitation after prostate cancer treatment. Understanding how these drugs interact with prostate cancer is therefore crucial.

Research has shown that PDE5 is expressed in prostate tissue, and intriguingly, some prostate cancer samples show higher PDE5 levels than normal or benign hyperplastic tissue. While this doesn't necessarily mean that PDE5 inhibitors would help fight cancer, it does suggest that the enzyme plays some role in prostate cell behavior.

The real breakthrough came from studies examining how tadalafil affects androgen receptors in prostate cancer cells. Prostate cancer is typically "androgen-sensitive," meaning it depends on male hormones like testosterone to grow. The standard treatment for advanced prostate cancer—androgen deprivation therapy (ADT)—works by cutting off this hormonal fuel supply.

However, cancer cells often become resistant to ADT, leading to a deadly condition called castration-resistant prostate cancer. One way cancer cells evade treatment is by reducing their androgen receptor expression, making them less dependent on—and less vulnerable to the loss of—male hormones.

Here's where tadalafil enters the picture. Laboratory studies found that tadalafil increases androgen receptor expression in prostate cancer cells. While this might sound counterproductive, it actually has a potentially beneficial effect: it makes the cancer cells more sensitive to anti-androgen treatments like bicalutamide. In other words, tadalafil might help keep prostate cancer cells in a treatable state.

The researchers also discovered that anti-androgen treatment increases aromatase expression in prostate cancer cells, which could lead to increased local estrogen production. Estrogen signaling through certain receptors may promote cancer progression. Tadalafil appeared to block this aromatase increase, potentially preventing this escape mechanism.

When prostate cancer cells were treated with both bicalutamide and tadalafil, the combination showed enhanced anti-proliferative effects compared to either drug alone. This suggests that tadalafil might serve as a valuable adjunct to standard androgen deprivation therapy, helping to maintain treatment effectiveness.

It's important to note that these findings come primarily from laboratory studies on cell lines, not from clinical trials in patients. Other research has shown that at clinically relevant doses, PDE5 inhibitors don't directly affect prostate cancer cell growth or migration. The potential benefits appear to lie in enhancing the effectiveness of hormone therapy rather than directly killing cancer cells.

The Bigger Picture: One Drug, Multiple Benefits​

What makes these findings particularly compelling is the emerging pattern. Across different tissues—fat, bone, and prostate—tadalafil appears to work by modulating steroid hormone pathways. It affects aromatase (the enzyme that converts testosterone to estrogen) and androgen receptor expression in tissue-specific ways that could provide therapeutic benefits.

In fat cells, tadalafil stimulates aromatase expression in a way that promotes healthier fat cell development. In bone cells, it inhibits aromatase while boosting androgen receptors, potentially favoring bone formation. In prostate cancer cells, it increases androgen receptor expression in a way that may enhance the effectiveness of anti-androgen therapy. This tissue-specific modulation of hormone signaling represents a sophisticated mechanism that goes far beyond simple blood vessel dilation.

The researchers describe tadalafil as acting like a "selective modulator of steroid hormone production"—a term that highlights its nuanced effects across different organ systems. This versatility suggests that men taking tadalafil for erectile dysfunction may be receiving additional health benefits they (and their doctors) weren't aware of.

Looking Forward: What This Means for Patients​

Before getting too excited, it's important to acknowledge the limitations of current research. Much of what we know comes from laboratory studies on cells and animal models. While multiple clinical trials have shown benefits for metabolic parameters, we don't yet have large-scale clinical trials specifically designed to test whether tadalafil can prevent osteoporosis or enhance prostate cancer treatment in humans.

However, the consistency of findings across different research approaches is encouraging. The fact that a drug already approved and widely used shows potential benefits beyond its intended purpose is exciting for several reasons. First, we already know a great deal about tadalafil's safety profile from decades of clinical use. Second, if these additional benefits are confirmed, they wouldn't require developing an entirely new medication—we would simply be finding new applications for an existing tool.

For men already taking tadalafil for erectile dysfunction or urinary symptoms, these findings suggest they may be receiving bonus health benefits. For researchers and clinicians, they point toward promising new directions for treating obesity, osteoporosis, and prostate cancer—conditions that affect millions of people worldwide.

The story of tadalafil reminds us that medications often have effects beyond their original intended use, and that careful observation and scientific curiosity can uncover important new therapeutic applications. What started as a drug for improving sexual function may ultimately prove valuable for maintaining metabolic health, preserving bone strength, and fighting cancer—a remarkable evolution for a medication that many people still think of as simply "that little pill."

The Bottom Line: Tadalafil, the medication millions of men take for erectile dysfunction, appears to have significant effects on fat metabolism, bone health, and prostate cancer biology. While more clinical research is needed, the evidence suggests that this common medication may offer benefits far beyond the bedroom, potentially helping to combat some of the most challenging health issues facing aging adults.

Source: Greco EA, Antinozzi C, Di Luigi L, Aversa A, Sgrò P. Tadalafil and Steroid Hormones Interactions in Adipose, Bone and Prostate Tissues: Focus on Translational Perspectives. Int. J. Mol. Sci. 2022, 23, 4191.
 

ExcelMale Newsletter Signup

Online statistics

Members online
4
Guests online
588
Total visitors
592

Latest posts

Beyond Testosterone Podcast

Back
Top