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Nitric Oxide as a Mediator of Relaxation of the Corpus Cavernosum in Response to Nonadrenergic, Noncholinergic Neurotransmission
Open accessAbstract
BACKGROUND: Nitric oxide has been identified as an endothelium-derived relaxing factor in blood vessels. We tried to determine whether it is involved in the relaxation of the corpus cavernosum that allows penile erection. The relaxation of this smooth muscle is known to occur in response to stimulation by nonadrenergic, noncholinergic neurons. METHODS: We studied strips of corpus cavernosum tissue obtained from 21 men in whom penile prostheses were inserted because of impotence. The mounted smooth-muscle specimens were pretreated with guanethidine and atropine and submaximally contracted with phenylephrine. We then studied the smooth-muscle relaxant responses to stimulation by an electrical field and to nitric oxide. RESULTS: Electrical-field stimulation caused a marked, transient, frequency-dependent relaxation of the corpus cavernosum that was inhibited in the presence of N-nitro-L-arginine and N-amino-L-arginine, which selectively inhibit the biosynthesis of nitric oxide from L-arginine. The addition of excess L-arginine, but not D-arginine, largely reversed these inhibitory effects. The specific liberation of nitric oxide (by S-nitroso-N-acetylpenicillamine) caused rapid, complete, and concentration-dependent relaxation of the corpus cavernosum. The relaxation caused by either electrical stimulation or nitric oxide was enhanced by a selective inhibitor of cyclic guanosine monophosphate (GMP) phosphodiesterase (M&B 22,948). Relaxation was inhibited by methylene blue, which inhibits cyclic GMP synthesis. CONCLUSIONS: Our findings support the hypothesis that nitric oxide is involved in the nonadrenergic, noncholinergic neurotransmission that leads to the smooth-muscle relaxation in the corpus cavernosum that permits penile erection. Defects in this pathway may cause some forms of impotence.
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“NO synthesized by NOS in the endothelium diffuses into the vessel wall where it activates sGC in vascular smooth muscle; this leads to a rise in cyclic GMP (cGMP) and elicits relaxation of the vessel [96-102].”
From Regulation of obesity and insulin resistance by nitric oxide (2014) · cites this paper as [99]
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Physiology and Pharmacology of Erectile Dysfunction
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Behzadi, M. K., Alimoradi, H., Javanmard, S. H., Sharifi, M. R., Rahimi, N., & Dehpour, A. R. (2012) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2012.12.021 · Cited by 3
“Although the exact mechanisms are still unknown, NO and EDHF pathways are known to be responsible for this (Büssemaker et al., 2003; Quesada et al., 2002; Rajfer et al., 1992; Sarac et al., 2006).”
BackgroundAndersen, M. L., Perry, J. C., Ishikura, I. A., & Tufik, S. (2006) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2006.12.012 · Cited by 3
“Drug-treated males were unable to achieve vaginal intromissions during most mounts, and had fewer penile erections (Moses and Hull, 1999) suggesting that NO promotes erection in intact males probably by mediating the filling of the corpora cavernosa of the penis (Rajfer et al., 1992).”
BackgroundGuha, T., Kohad, H., & Bhar, R. (2015) · Journal of Microscopy and Ultrastructure · doi:10.1016/j.jmau.2015.11.005 · Cited by 3
SEXUAL ACTIVITY CARDIOLOGICAL SURVEY ON MEMBERS OF THE ISRAEL HEART SOCIETY
Roth, A., Malov, N., & Survey, S. (2003) · International Journal of Clinical Practice · doi:10.1111/j.1742-1241.2003.tb10486.x · Cited by 3
Bhasin, S., & Benson, G. S. (2006) · Elsevier eBooks · doi:10.1016/b978-012515400-0/50029-4 · Cited by 3
Effect of increasing nitric oxide and dihydrotestosterone byTaraxacum coreanumextract
Mo, S. (2019) · Journal of Applied Biological Chemistry · doi:10.3839/jabc.2019.042 · Cited by 3
“음경 발기를 위한 음경해면체평활근의 이완은 비아드레날 린성 비콜린성 신경전달물질과 해면체 내피세포에서 분비되는 이완물질(endothelium derived relaxing factor, EDRF)에 의해 유발된다[8].”
Metadata
- Authors
- Rajfer, J., Aronson, W. J., Bush, P. A., Dorey, F. J., & Ignarro, L. J.
- Affiliations
- University of California, Los Angeles (US)
- ORCID
- Aronson, William J.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 1992-01-09
- Volume
- 326
- Issue
- 2
- Pages
- 90-94
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2056147576
- Cited by
- 1,006
- References
- 30
- Citations by year
- 2026: 4 · 2025: 8 · 2024: 5 · 2023: 11 · 2022: 12 · 2021: 11 · 2020: 13 · 2019: 14 · 2018: 15 · 2017: 17 · 2016: 17 · 2015: 17 · 2014: 26 · 2013: 22 · 2012: 30
- FWCI
- 50.38
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01hl040922-11, 5r01hl035014-12)
- National Heart, Lung, and Blood Institute (HL-35014, HL 40922)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Sexual function and dysfunction studies
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Health Sciences › Medicine › Urology › Urinary Bladder and Prostate Research
- Keywords
- nitric oxide, corpus cavernosum, penile erection, non-adrenergic non-cholinergic neurotransmission, smooth muscle relaxation, erectile dysfunction, cyclic GMP, L-arginine, methylene blue, penile prosthesis, electrical field stimulation
- MeSH terms
- Adult, Aged, Arginine, Electric Stimulation, Cyclic GMP, Humans, Erectile Dysfunction, Male, Methylene Blue, Middle Aged, Muscle Relaxation, Muscle, Smooth, Synaptic Transmission, Nitric Oxide, Organ Culture Techniques, Penile Erection, Penis, Purinones, Nitroarginine
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