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Stress Affects a Gastrin-Releasing Peptide System in the Spinal Cord That Mediates Sexual Function: Implications for Psychogenic Erectile Dysfunction

BACKGROUND: Many men suffering from stress, including post-traumatic stress disorder (PTSD), report sexual dysfunction, which is traditionally treated via psychological counseling. Recently, we identified a gastrin-releasing peptide (GRP) system in the lumbar spinal cord that is a primary mediator f...

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Autores principales: Sakamoto, Hirotaka, Matsuda, Ken-Ichi, Zuloaga, Damian G., Nishiura, Nobuko, Takanami, Keiko, Jordan, Cynthia L., Breedlove, S. Marc, Kawata, Mitsuhiro
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2627921/
https://www.ncbi.nlm.nih.gov/pubmed/19169356
http://dx.doi.org/10.1371/journal.pone.0004276
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author Sakamoto, Hirotaka
Matsuda, Ken-Ichi
Zuloaga, Damian G.
Nishiura, Nobuko
Takanami, Keiko
Jordan, Cynthia L.
Breedlove, S. Marc
Kawata, Mitsuhiro
author_facet Sakamoto, Hirotaka
Matsuda, Ken-Ichi
Zuloaga, Damian G.
Nishiura, Nobuko
Takanami, Keiko
Jordan, Cynthia L.
Breedlove, S. Marc
Kawata, Mitsuhiro
author_sort Sakamoto, Hirotaka
collection PubMed
description BACKGROUND: Many men suffering from stress, including post-traumatic stress disorder (PTSD), report sexual dysfunction, which is traditionally treated via psychological counseling. Recently, we identified a gastrin-releasing peptide (GRP) system in the lumbar spinal cord that is a primary mediator for male reproductive functions. METHODOLOGY/PRINCIPAL FINDINGS: To ask whether an acute severe stress could alter the male specific GRP system, we used a single-prolonged stress (SPS), a putative rat model for PTSD in the present study. Exposure of SPS to male rats decreases both the local content and axonal distribution of GRP in the lower lumbar spinal cord and results in an attenuation of penile reflexes in vivo. Remarkably, pharmacological stimulation of GRP receptors restores penile reflexes in SPS-exposed males, and induces spontaneous ejaculation in a dose-dependent manner. Furthermore, although the level of plasma testosterone is normal 7 days after SPS exposure, we found a significant decrease in the expression of androgen receptor protein in this spinal center. CONCLUSIONS/SIGNIFICANCE: We conclude that the spinal GRP system appears to be a stress-vulnerable center for male reproductive functions, which may provide new insight into a clinical target for the treatment of erectile dysfunction triggered by stress and psychiatric disorders.
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spelling pubmed-26279212009-01-26 Stress Affects a Gastrin-Releasing Peptide System in the Spinal Cord That Mediates Sexual Function: Implications for Psychogenic Erectile Dysfunction Sakamoto, Hirotaka Matsuda, Ken-Ichi Zuloaga, Damian G. Nishiura, Nobuko Takanami, Keiko Jordan, Cynthia L. Breedlove, S. Marc Kawata, Mitsuhiro PLoS One Research Article BACKGROUND: Many men suffering from stress, including post-traumatic stress disorder (PTSD), report sexual dysfunction, which is traditionally treated via psychological counseling. Recently, we identified a gastrin-releasing peptide (GRP) system in the lumbar spinal cord that is a primary mediator for male reproductive functions. METHODOLOGY/PRINCIPAL FINDINGS: To ask whether an acute severe stress could alter the male specific GRP system, we used a single-prolonged stress (SPS), a putative rat model for PTSD in the present study. Exposure of SPS to male rats decreases both the local content and axonal distribution of GRP in the lower lumbar spinal cord and results in an attenuation of penile reflexes in vivo. Remarkably, pharmacological stimulation of GRP receptors restores penile reflexes in SPS-exposed males, and induces spontaneous ejaculation in a dose-dependent manner. Furthermore, although the level of plasma testosterone is normal 7 days after SPS exposure, we found a significant decrease in the expression of androgen receptor protein in this spinal center. CONCLUSIONS/SIGNIFICANCE: We conclude that the spinal GRP system appears to be a stress-vulnerable center for male reproductive functions, which may provide new insight into a clinical target for the treatment of erectile dysfunction triggered by stress and psychiatric disorders. Public Library of Science 2009-01-26 /pmc/articles/PMC2627921/ /pubmed/19169356 http://dx.doi.org/10.1371/journal.pone.0004276 Text en Sakamoto et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sakamoto, Hirotaka
Matsuda, Ken-Ichi
Zuloaga, Damian G.
Nishiura, Nobuko
Takanami, Keiko
Jordan, Cynthia L.
Breedlove, S. Marc
Kawata, Mitsuhiro
Stress Affects a Gastrin-Releasing Peptide System in the Spinal Cord That Mediates Sexual Function: Implications for Psychogenic Erectile Dysfunction
title Stress Affects a Gastrin-Releasing Peptide System in the Spinal Cord That Mediates Sexual Function: Implications for Psychogenic Erectile Dysfunction
title_full Stress Affects a Gastrin-Releasing Peptide System in the Spinal Cord That Mediates Sexual Function: Implications for Psychogenic Erectile Dysfunction
title_fullStr Stress Affects a Gastrin-Releasing Peptide System in the Spinal Cord That Mediates Sexual Function: Implications for Psychogenic Erectile Dysfunction
title_full_unstemmed Stress Affects a Gastrin-Releasing Peptide System in the Spinal Cord That Mediates Sexual Function: Implications for Psychogenic Erectile Dysfunction
title_short Stress Affects a Gastrin-Releasing Peptide System in the Spinal Cord That Mediates Sexual Function: Implications for Psychogenic Erectile Dysfunction
title_sort stress affects a gastrin-releasing peptide system in the spinal cord that mediates sexual function: implications for psychogenic erectile dysfunction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2627921/
https://www.ncbi.nlm.nih.gov/pubmed/19169356
http://dx.doi.org/10.1371/journal.pone.0004276
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