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Mechanistic analysis of erectile dysfunction in a depression rat model

OBJECTIVE: Most men suffering from depression have different degrees of erectile dysfunction (ED), but the relationship between depression and ED is not clear. This study explored the effect of depression on erectile function in rats and the underlying mechanism. METHODS: The potential targets and k...

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Autores principales: Hong, Zhi-ming, Chen, Zi-long, Feng, Jun-long, Wang, Sheng-jie, Qiu, Jun-feng, Zeng, Yang-ling, Wang, Quan, Wang, Ji-sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9152200/
https://www.ncbi.nlm.nih.gov/pubmed/35615771
http://dx.doi.org/10.1177/03000605221100334
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author Hong, Zhi-ming
Chen, Zi-long
Feng, Jun-long
Wang, Sheng-jie
Qiu, Jun-feng
Zeng, Yang-ling
Wang, Quan
Wang, Ji-sheng
author_facet Hong, Zhi-ming
Chen, Zi-long
Feng, Jun-long
Wang, Sheng-jie
Qiu, Jun-feng
Zeng, Yang-ling
Wang, Quan
Wang, Ji-sheng
author_sort Hong, Zhi-ming
collection PubMed
description OBJECTIVE: Most men suffering from depression have different degrees of erectile dysfunction (ED), but the relationship between depression and ED is not clear. This study explored the effect of depression on erectile function in rats and the underlying mechanism. METHODS: The potential targets and key signaling pathways of depression and ED were predicted through bioinformatics analysis, and a depression rat model was established by inducing chronic restraint stress. Pathological changes in rat penis tissue were studied by hematoxylin and eosin staining. The serum dopamine level was quantified by an enzyme-linked immunosorbent assay. The expression of related proteins and mRNA was detected by western blotting and real-time quantitative reverse transcription-polymerase chain reaction. RESULTS: Hematoxylin and eosin staining showed pathological damage in the penile tissue of the model group rats. The serum dopamine level, dopamine receptor D2 (DRD2) and solute carrier family 6 member 3 (SLC6A3) protein levels in penile tissue, and DRD2 and SLC6A3 mRNA levels were lower in the model group than in the control group. CONCLUSION: The decrease in erectile function in the depression rat model was related to dysfunction of the dopamine system and dopaminergic synapse signaling pathway.
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spelling pubmed-91522002022-06-01 Mechanistic analysis of erectile dysfunction in a depression rat model Hong, Zhi-ming Chen, Zi-long Feng, Jun-long Wang, Sheng-jie Qiu, Jun-feng Zeng, Yang-ling Wang, Quan Wang, Ji-sheng J Int Med Res Pre-Clinical Research Report OBJECTIVE: Most men suffering from depression have different degrees of erectile dysfunction (ED), but the relationship between depression and ED is not clear. This study explored the effect of depression on erectile function in rats and the underlying mechanism. METHODS: The potential targets and key signaling pathways of depression and ED were predicted through bioinformatics analysis, and a depression rat model was established by inducing chronic restraint stress. Pathological changes in rat penis tissue were studied by hematoxylin and eosin staining. The serum dopamine level was quantified by an enzyme-linked immunosorbent assay. The expression of related proteins and mRNA was detected by western blotting and real-time quantitative reverse transcription-polymerase chain reaction. RESULTS: Hematoxylin and eosin staining showed pathological damage in the penile tissue of the model group rats. The serum dopamine level, dopamine receptor D2 (DRD2) and solute carrier family 6 member 3 (SLC6A3) protein levels in penile tissue, and DRD2 and SLC6A3 mRNA levels were lower in the model group than in the control group. CONCLUSION: The decrease in erectile function in the depression rat model was related to dysfunction of the dopamine system and dopaminergic synapse signaling pathway. SAGE Publications 2022-05-25 /pmc/articles/PMC9152200/ /pubmed/35615771 http://dx.doi.org/10.1177/03000605221100334 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Pre-Clinical Research Report
Hong, Zhi-ming
Chen, Zi-long
Feng, Jun-long
Wang, Sheng-jie
Qiu, Jun-feng
Zeng, Yang-ling
Wang, Quan
Wang, Ji-sheng
Mechanistic analysis of erectile dysfunction in a depression rat model
title Mechanistic analysis of erectile dysfunction in a depression rat model
title_full Mechanistic analysis of erectile dysfunction in a depression rat model
title_fullStr Mechanistic analysis of erectile dysfunction in a depression rat model
title_full_unstemmed Mechanistic analysis of erectile dysfunction in a depression rat model
title_short Mechanistic analysis of erectile dysfunction in a depression rat model
title_sort mechanistic analysis of erectile dysfunction in a depression rat model
topic Pre-Clinical Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9152200/
https://www.ncbi.nlm.nih.gov/pubmed/35615771
http://dx.doi.org/10.1177/03000605221100334
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