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Beyond testosterone cypionate: evidence behind the use of nandrolone in male health and wellness
Michael M. Pan and Jason R. Kovac
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Abstract
Characterized by low serum testosterone levels and diverse symptoms, male hypogonadism is a common condition. Current medical treatment focuses on testosterone supplementation using multiple modalities such as injections, gels and pellets. Interestingly, while testosterone is considered an anabolic androgenic steroid, it has not been saddled with the social stigma that other, similar medications have. The goal of this review is to highlight an anabolic steroid, 19-nortestosterone (i.e., nandrolone, deca-durabolin) and illustrate prospective therapeutic applications for male health. Containing a chemical structure similar to testosterone, nandrolone has a higher myotrophic: androgenic ratio resulting in improved effects on muscle mass. Animal models have suggested application in the improvement of joint healing following rotator cuff repair. Minimal literature exists regarding the use of nandrolone and, as such, further human studies are required.
Keywords: Nandrolone, erectile dysfunction (ED), testosterone supplementation therapy (TST), alopecia, joint healing, pharmacology, muscle growth
Introduction
Male hypogonadism is a clinical entity characterized by symptoms such as fatigue, erectile dysfunction (ED) and mood changes associated with decreased serum levels of testosterone (1). Treatment of hypogonadism involves the exogenous supplementation of testosterone and may be complemented with other medications such as human chorionic gonadotropin (hCG) and clomiphene citrate (clomid) (2-4). With the increasing rise in incidence of male hypogonadism, and the growing knowledge of the roles for testosterone in male health, other pharmacological steroid compounds should be evaluated to either supplement, and/or replace testosterone in the treatment of male health.
Unfortunately, numerous well-published media reports dealing with anabolic steroids in professional and Olympic athletes have brought a cloud of speculation and doubt regarding use of these “illicit” medications. The fact that these anabolic steroid medications are banned by numerous athletic associations such as the International Olympic Committee as well as the National Football and Basketball Associations and Major League Baseball, further re-enforces the public perception that these medications should not be used under any circumstances. Indeed, a recent study (5) evaluated healthcare-provider attitudes towards anabolic androgenic steroids (AAS) and found that AAS users were viewed less favorably that cocaine abusers or healthy adults. These perceptions were enhanced by the passage of the Anabolic Steroid Control Act of 2004 that listed anabolic steroids as schedule III controlled substances—similar to ketamine, opiates and morphine (6). This policy mandated that a physician prescription was necessary to obtain the medication; further challenging the opinion of the general public. As such, it is tempting to speculate that investigations into alternatives to testosterone therapy have been slowed by societal stigma and perception.
An anabolic steroid that has been investigated to some degree in the treatment of male health is 19-nortestosterone (or nandrolone, deca-durabolin). This synthetic anabolic steroid has been available for decades and has been studied in multiple clinical pathologies. Early investigations of nandrolone focused on its potential uses in the treatment of osteoporosis. In that setting, it increased gastrointestinal and renal tubular absorption of calcium and decreased bone reabsorption (7). Nandrolone also had the beneficial effects of stimulating the formation of extra-osseous collagen and soft tissue (7). However, as would be expected, ~50% of women who were prescribed nandrolone reported some component of virilization (7). Due, in part, to these adverse effects, and the development of newer and more effective therapies to treat osteoperosis (i.e., bisphosphonates), nandrolone never gained traction as an effective clinical adjunct for this indication. Despite this, nandrolone’s stimulatory effects on bone and soft tissues became the basis upon which some researchers suggested its use in anemia and muscle wasting secondary to hemodialysis and/or HIV (8,9). Furthermore, recent studies have investigated the effects of nandrolone in the treatment of chronic pulmonary obstructive disease (10,11). In the context of the current review that examines the potential uses for anabolic steroids in male health, nandrolone was chosen as a case study. Details regarding its pharmacology as well as its potential uses in male health were explored.
Materials and methods
A PubMed/MEDLINE literature search was conducted for the periods of 1960–2015 in January, 2015. There were an insignificant number of published quality data available for meta-analysis, so a systematic review was performed. Key search terms included combinations of “Nandrolone”, “testosterone”, “hypogonadism”, “deca-durabolin”, “19-nortestosterone”, “pharmacology”, “alopecia”, “joint(s)”, “rotator cuff”, and “erectile dysfunction”. In excess of 1,000 manuscript abstracts were screened by the authors using title search and abstract summaries. Applicable studies were read in-depth and included in this current review. Additionally, an internet search strategy examining blogs and discussion sites, as previously described (12) was used. These techniques have been previously validated through other reports that employed similar methods of Internet data mining to report consistent findings (13,14).
Nandrolone pharmacology
Nandrolone is a synthetic anabolic steroid that bears similarity in chemical appearance to testosterone. The only major difference between the two molecules is a single methyl group (see Figure 1). Similar to testosterone, nandrolone is administered via intramuscular (IM) injection and has a plasma half-life of approximately 8 days (7). Nandrolone binds to androgen receptors with a greater binding affinity than testosterone and with an increased anabolic, or myotrophic, activity rate (versus androgenic activity) (15). For example and to assist in comparison, the myotrophic:androgenic ratio can be used to compare testosterone (~1:1) to nandrolone (~11:1) (15) with regards to the ability to stimulate muscle growth compared to virilization.
Figure 1
Comparison of molecular structures of testosterone and 19-nortestosterone (nandrolone).
With regards to the mechanisms of nandrolone inside the human body, understanding the pathway of testosterone action is important. In certain tissues, such as the prostate or in the hair follicles, testosterone is converted to dihydrotestosterone (DHT) by 5 alpha-reductase (5AR). High levels of 5AR activity are present in androgenic tissues from the prostate but are undetectable in skeletal muscle (15). As such, in skeletal muscle, testosterone directly binds androgen receptors contributing to muscle growth. However, in prostatic tissues and hair follicles, testosterone is converted to DHT by 5AR and is thus responsible for the known side effects of testosterone supplementation therapy (TST) on prostate growth and alopecia (15).
5AR can also act on nandrolone (19-nortestosterone) to produce 5α-dihydro-19-nortestosterone (15). This reduced form of nandrolone has a significantly decreased binding affinity for the androgen receptor compared to its parent steroid, testosterone (15). As such, the 5AR conversion of nandrolone to 5α-dihydro-19-nortestosterone in prostatic tissues results in a significantly decreased ability of nandrolone to bind androgen receptors. Theoretically, the end result could be a decrease in prostatic growth with a possible and theoretical effect on lower urinary tract symptoms such as those developed as a result of benign prostatic hyperplasia (BPH). A potential decrease in the rates of alopecia could also be observed . Furthermore, the lack of 5AR in skeletal muscle allows nandrolone to bind strongly to androgen receptors in the muscle and stimulate growth, contributing to its high myotrophic:androgenic ratio (15).
The metabolism of nandrolone is incompletely understood. Metabolites of nandrolone include 19-norandrosterone and 19-noretiocholanolone glucuronides that are detectable in urine (16). Animal studies suggest that nandrolone can also be converted to various estrogens via the actions of aromatase (17,18); however, human studies are lacking.
Nandralone and alopecia
TST in hypogonadal men results in elevated levels of free serum testosterone and, in turn, DHT. This occurs due to conversion of testosterone to DHT via 5AR inhibitors (5ARi) (19,20). Androgenic alopecia, or male pattern hair loss, typically occurs in 20% of 20-year-old men and then increases by approximately 10% every 10 years (21). A critical role for DHT in hair growth can be seen in the case study of men with Imperato-McGinley syndrome. This condition results from a mutation in the gene for type II 5AR that prevents the expression of the enzyme. As a consequence, men with this condition never become bald (22).
Androgen dependent miniaturization of scalp hair follicles by DHT is implicated as the primary cause of alopecia (23). Controlled clinical trials demonstrated that use of finasteride resulted in decreased accumulation of DHT and improvements in both subjective and objective assessments of hair growth and density (23).
Indeed, the most established management paradigm for the treatment of alopecia in the male is finasteride (24). First approved in 1992 in the treatment of benign prostatic hypertrophy, finasteride was approved for the treatment of alopecia in 1997 at a dose of 1 mg daily (propecia®) (24). In men on TST, finasteride at 1 mg is used as a means of preventing the excess exogenously administered testosterone from converting to DHT. By decreasing the amount of DHT, less is available to act on the hair follicles stabilizing the amount of hair loss.
The theory underlying the possible use of nandrolone in the context of alopecia results from the fact that it does not convert to DHT but instead gets transformed into 5α-dihydro-19-nortestosterone, a molecularly distinct compound (15,25). It is thus possible that in hypogonadal males nandrolone, in addition to or in replacement for testosterone, could alleviate concerns for the development of androgenic alopecia.
There are several lines of evidence that make this hypothesis particularly appealing. In experimental animal models, nandrolone is synthesized endogenously through a mechanism distinct from DHT (25). Furthermore, the metabolism of nandrolone in animal models yields compounds completely unrelated to DHT (15,26). It has also been proven that the actions of 5AR on nandrolone produce a compound that has decreased affinity and activity at the androgen receptor (15). Given that nandrolone is not converted to DHT it seems logical to assume that it would have less effect on hair loss than exogenous testosterone (with its subsequent conversion to DHT). Thus, nandrolone may be beneficial in treating hypogonadal men concerned about alopecia in the setting of TST.
Another aspect of this discussion also involves consideration for the possible existence of persistent sexual side effects and anxiety/depressive symptoms reported with the use of 5ARis like finasteride (27,28). Some symptoms of which have been shown to last for months to years (29). Therefore, by utilizing an agent with less direct effects on hair loss, nandrolone may represent a viable option for men in the treatment of hypogonadism. Altered levels of neuroactive steroids related to depressive symptoms have been identified in men with a history of finasteride use, even when the drug has been discontinued (30). The use of nandrolone would obviate these concerns.
Nandrolone and joint healing
Recent studies in animal models have identified a potential role for nandrolone in joint pain, particularly post rotator cuff tears (31,32). In one such study by Gerber et al. (31), 20 New Zealand white rabbits had their supraspinatus tendon released with musculotendinous retraction and observed over 6 weeks. Rabbits were organized into groups treated with placebo as well as local and systemic administration of nandrolone (31). Nandrolone, given in the phase after tendon release, was found to inhibit fatty infiltration of the supraspinatus muscle and reduced functional impairment of the rotator cuff (31).
An earlier 2010 study by Papaspiliopoulos et al. (32) examined 48 male rabbits that underwent rotator cuff incision and reconstruction after stratification into groups based on local nandrolone administration and immobilization. In this study, local administration of nandrolone proved detrimental to wound healing however, systemic administration was not studied (32). Other limitations include the fact that anabolic steroids affect the tensile strength of tendons that may then cause failure with less elongation (33). Local administration of nandrolone may impair the healing of acute tendon injuries and the perceived benefits to retracted muscle may be outweighed by its effects on tendon healing (34).
Interestingly, Internet and discussion group anecdotal data suggests that nandrolone is effective in decreasing joint pain in bodybuilders. These athletes lift large amounts of weights putting extreme pressure on their joints while reporting improvement and lowered pain with the use of nandrolone. While limited data is available, and dosages are unknown, further investigations are needed to determine the effects of nandrolone on joints in general, and the rotator cuff in particular.
Nandrolone and muscle growth
Nandrolone has long been known to have significant stimulatory effects on muscle growth. As described above, nandrolone displays a greater myotrophic:androgenic ratio compared to testosterone (15). When compared to testosterone, the high levels of 5AR in androgenic tissues (i.e., the prostate) convert nandrolone to a less active metabolite (versus DHT that is highly active). Furthermore, the lack of 5AR in skeletal muscle allows nandrolone to produce a primarily anabolic/myotrophic (i.e., muscle growing) effect (15). The ability of nandrolone to preferentially stimulate muscle growth formed the basis of its use in the treatment of anorexia and cachexia in patients with chronic medical disorders such as chronic renal failure and HIV (8,35). In these patients, administration of nandrolone has been shown to increase lean body mass as well as muscle mass and strength (8,35).
Hypogonadism has been shown to be associated with dyslipidemia, atherosclerosis, cardiovascular disease, metabolic syndrome, and diabetes (36). Testosterone supplementation in hypogonadal men improves these risk factors leading, in some patients, to complete resolution of their metabolic syndrome (36-38). Indeed, an increase in lean body mass and muscle mass with the systemic administration of nandrolone could improve body composition and augment testosterone’s effects in preventing (39) and reversing metabolic syndrome and the risk of type 2 diabetes in hypogonadal men.
Nandralone and ED
In spite of its potential beneficial uses described above, one major limitation to the use of nandrolone in hypogonadal males stems from the fact that a relationship may exist between the use of nandrolone and ED. Although the World Health Organization INCHEM database compiled by the International Program on Chemical Safety (http://www.who.int/ipcs/en) lists impotence under adverse effects of nandrolone; no consistent reports of ED associated with the use of nandrolone have been reported in the literature.
Anecdotal evidence from patients, as well as those men who have previously used nandrolone from “alternative” sources suggests a relationship with the use of nandrolone (alone, not in combination with testosterone) and ED. Indeed, nandrolone may contribute to the development of ED through two mechanisms: the suppression of testosterone/DHT via negative feedback and the buildup of estrogens.
Numerous studies have shown that DHT is the active androgen involved in maintenance of nitric oxide-mediated penile erections. Castrated rats treated with exogenous testosterone recovered erectile function but, when co-administered with a 5ARi to block DHT production, this recovery was lost (40,41). Moreover, administration of transdermal DHT in aging men resulted in improvement in early morning erections and the ability to maintain erections (42). In fact, one of the most common sexual side-effects of 5ARi’s (described above) is ED (43).
Nandrolone has also been shown to decrease LH, FSH, and endogenous testosterone levels in animal models, indicating a negative feedback loop to inhibit the hypothalamic-pituitary-gonadal (HPG) axis (44). In this context, nandrolone acts as an androgen receptor agonist that is not converted endogenously to DHT (15). As such, it provides negative feedback to the HPG axis to suppresses testosterone levels, further decreasing the available testosterone and DHT, compounding its negative effects on erectile function.
Imbalance in the testosterone to estrogen ratio has been associated with ED (45). Numerous subsets of patients with ED have elevated estradiol levels, indicating a relationship between estrogens and erectile function (45). Nandrolone and other members of the 19-nor-androgen families have been shown to undergo aromatase-mediated conversion to estrogens in animal models (17,18,46). Nandrolone itself shows significant binding affinity and full agonist activity with the alpha-estrogen receptor (47). Indeed, increased serum estrogen levels in men have been associated with development of gynecomastia, increased body fat mass, and unfavorable lipid profiles—all contributing factors to ED (48-51). As such, it can be theorized that nandrolone should be administered with testosterone to prevent ED with an eye towards regulation of a patients estradiol levels. However, specific in vivo studies examining the effects of nandrolone administration in humans has not been described.
Nandralone and male infertility
No studies currently exist.
Discussion
Nandrolone is a synthetic anabolic steroid that possesses unique qualities and is potentially beneficial in the treatment of male health alone, or as an adjunct to TST for hypogonadal men. Nandrolone has a relatively long half-life in the plasma and a strong binding affinity for androgen receptors. The lack of conversion to DHT could mean decreased hair loss in men undergoing TST suggesting a novel use for this medication in a subpopulation of hypogonadal men. Furthermore, in men with voiding dysfunction due to benign prostatic hypertrophy, the reduction of nandrolone by 5AR to generate a weaker androgen (compared to DHT) that does not stimulate the growth of androgenic tissues such as the prostate could serve as another indicator for its use. Nandrolone preferentially stimulates growth of skeletal muscle and lean body mass that may provide benefit in reducing components of metabolic syndrome. Moreover, preliminary work on nandrolone has suggested a potential role in the treatment of joint healing, particularly in rotator cuff injuries.
Limitations to the use of nandrolone include the potential for ED via suppression of the HPG axis. The lack of conversion to DHT and the concurrent increase in serum estrogens may mediate this effect. Administration of low doses of testosterone, along with nandrolone, would alleviate these effects. Further research is needed to evaluate nandrolone’s potential role in the management of male health.
Conclusions
Characterized by low serum testosterone and a multitude of debilitating symptoms, male hypogonadism is a common condition. Primarily treated with exogenous testosterone replacement, novel adjuncts to improve responses and decrease side effects are being studied. Nandrolone is an anabolic steroid compound with a high myotrophic:anabolic ratio. In this manuscript, we have explored the potential uses for nandrolone in male health. Specifically, we have reviewed the pharmacology of nandrolone and detailed a potential role for nandrolone in joint healing and muscle growth. Finally, a consideration was given to the potential adverse effects of nandrolone on ED. Further research in human subjects is required.
Acknowledgements
None.
Footnotes
Conflicts of Interest: JR Kovac is a paid speaker for AbbVie. The other author has no conflicts of interest to declare.
Article information
Transl Androl Urol. 2016 Apr; 5(2): 213–219.
doi: 10.21037/tau.2016.03.03
PMCID: PMC4837307
Michael M. Pan1 and Jason R. Kovac
1Scott Department of Urology, Baylor College of Medicine, Houston, Texas 77030, USA; 2Men’s Health Center, Urology of Indiana, Indianapolis, Indiana 46260, USA
Contributions: (I) Conception and design: All authors; (II) Administrative support: All authors; (III) Provision of study materials or patients: All authors; (IV) Collection and assembly of data: All authors; (V) Data analysis and interpretation: All authors; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.
Correspondence to: Dr. Jason R. Kovac. Men’s Health Center, 8240 Naab Road, Suite 220, Indianapolis, Indiana 46260, USA. Email: moc.niygoloru@cavokj.
Received 2016 Jan 11; Accepted 2016 Feb 29.
Copyright 2016 Translational Andrology and Urology. All rights reserved.
Articles from Translational Andrology and Urologyare provided here courtesy of AME Publications
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