Cited by 69Sexual function and dysfunction studiesUrinary Bladder and Prostate ResearchUrological Disorders and Treatments

The effects of chronic 5-alpha-reductase inhibitor (dutasteride) treatment on rat erectile function

Pinsky, Michael R., Gur, Serap, Tracey, Anthony J., Harbin, Andrew, Hellstrom, Wayne J.G.·2011·The Journal of Sexual Medicine

Abstract

Introduction: Numerous clinical series have reported an association between 5-alpha-reductase inhibitors (5ARIs) and sexual dysfunction, but there are limited preclinical data available. Aim: To further investigate the mechanisms of erectile dysfunction (ED) related to 5ARI therapy using a rat model. Main Outcome Measures: Outcome measures include serum dihydrotestosterone (DHT), relaxant and contractile properties of cavernosal muscle, and nitric oxide synthase expression. Methods: Twenty adult male Sprague-Dawley rats were randomized into control (N = 10) and dutasteride (0.5 mg/rat/day, in drinking water, N = 10) groups. Serum samples were obtained at baseline, from which DHT was measured after 30 days of treatment via radioimmunoassay (Beckman Coulter, Fullerton, CA, USA). Before the terminal blood draw, erectile response was measured using cavernosal nerve stimulation. The relaxant and contractile properties of cavernosal muscle strips were evaluated in tissue baths, and immunohistochemical (IHC) staining for nitric oxide synthase (NOS) and collagen deposition was performed. Results: Mean serum DHT was suppressed by 86.5% (range 64.2–94.8%) after 30 days of 5ARI treatment and was statistically significant (P = 0.0024). In vivo erectile response in the dutasteride treated group decreased significantly compared with control (P < 0.001). While electrical field stimulation (EFS)-induced and acetylcholine-induced relaxation was decreased, EFS-induced and phenlyephrine-induced adrenergic contraction was significantly enhanced in the dutasteride group (P < 0.01). IHC studies demonstrated increased collagen deposition in the treatment arm as well as altered expression of neuronal NOS (nNOS) and inducible NOS (iNOS). Conclusions: The 5ARIs, as demonstrated in these rat cavernosal smooth muscle studies, have a detrimental effect on erectile function. Enhanced iNOS expression may protect penile smooth muscle from fibrosis. The effect of 5ARIs on human sexual function warrants further investigation.

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Crossref · 10.1111/j.1743-6109.2011.02425.x

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Authors
Pinsky, M. R., Gur, S., Tracey, A. J., Harbin, A., & Hellstrom, W. J. G.
Affiliations
  • Tulane University (US)
  • Department of Urology, Tulane Health Sciences Center , New Orleans, LA , USA
Corresponding author
Hellstrom, Wayne J.G.
Venue
The Journal of Sexual Medicine
Published
2011-11-01
Volume
8
Issue
11
Pages
3066-3074
ISSN
  • 1743-6095 (ISSN-L)
  • 1743-6109
OpenAlex
W1542310964
Cited by
69
References
21
Citations by year
2026: 3 · 2025: 2 · 2024: 2 · 2023: 5 · 2022: 4 · 2021: 6 · 2020: 6 · 2019: 5 · 2018: 3 · 2017: 3 · 2016: 6 · 2015: 5 · 2014: 4 · 2013: 5 · 2012: 9
FWCI
3.94
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Sexual Medicine (publishedVersion)
  • PubMed (publishedVersion)
Funders
Sexual Medicine Society of North America
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Sexual function and dysfunction studies
  • Health Sciences › Medicine › Urology › Urinary Bladder and Prostate Research
  • Health Sciences › Medicine › Urology › Urological Disorders and Treatments
Keywords
dutasteride, 5-alpha reductase inhibitors, erectile dysfunction, dihydrotestosterone, corpus cavernosum smooth muscle, nitric oxide synthase, inducible nitric oxide synthase, neuronal nitric oxide synthase, collagen deposition, penile fibrosis, sexual dysfunction, rat model
MeSH terms
Dutasteride, Animals, Azasteroids, Isometric Contraction, Male, Muscle, Smooth, Vascular, Penile Erection, Penis, Rats, Sprague-Dawley, Rats, Nitric Oxide Synthase Type II, Nitric Oxide Synthase Type I, 5-alpha Reductase Inhibitors

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