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GYY4137 a H(2)S donor, attenuates ipsilateral epididymis injury in experimentally varicocele-induced rats via activation of the PI3K/Akt pathway

OBJECTIVE(S): The current study was aimed to investigate the effect of morpholin-4-ium 4 methoxyphenyl (morpholino) phosphinodithioate (GYY4137) on ipsilateral epididymis injury in a rat model of experimental varicocele (VC). MATERIALS AND METHODS: Sixty Wistar rats were randomly assigned to sham, s...

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Autores principales: Xia, Yu-qi, Ning, Jin-zhuo, Cheng, Fan, Yu, Wei-min, Rao, Ting, Ruan, Yuan, Yuan, Run, Du, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196355/
https://www.ncbi.nlm.nih.gov/pubmed/32373293
http://dx.doi.org/10.22038/ijbms.2019.30588.7372
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author Xia, Yu-qi
Ning, Jin-zhuo
Cheng, Fan
Yu, Wei-min
Rao, Ting
Ruan, Yuan
Yuan, Run
Du, Yang
author_facet Xia, Yu-qi
Ning, Jin-zhuo
Cheng, Fan
Yu, Wei-min
Rao, Ting
Ruan, Yuan
Yuan, Run
Du, Yang
author_sort Xia, Yu-qi
collection PubMed
description OBJECTIVE(S): The current study was aimed to investigate the effect of morpholin-4-ium 4 methoxyphenyl (morpholino) phosphinodithioate (GYY4137) on ipsilateral epididymis injury in a rat model of experimental varicocele (VC). MATERIALS AND METHODS: Sixty Wistar rats were randomly assigned to sham, sham plus GYY4137, VC and VC plus GYY4137 groups. Sperm quality parameters, including sperm count, motility and viability were evaluated after 4 weeks. Histological changes were measured by hematoxylin and eosin staining between the groups. The oxidative stress levels were estimated by determining epididymal superoxide dismutase (SOD) and malondialdehyde (MDA). The apoptosis status and the expression of phosphatidylinositol 3′-OH kinase (PI3K)/Akt were analyzed by immunohistochemical analysis, western blot and RT-qPCR. RESULTS: VC resulted in the decrease of sperm parameters, significant histological damage and higher levels of oxidative stress and apoptosis. Compared to the VC group, GYY4137 markedly ameliorated these observed changes. In addition, treatment with GYY4137 obviously reduced the levels of caspase-3 and Bax and increased the levels of the phosphorylation of PI3K p85 and Akt. CONCLUSION: Our data demonstrated that GYY4137 may alleviate the sperm damage and epididymis injury in experimentally VC-induced rats by activation of the PI3K/Akt pathway.
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spelling pubmed-71963552020-05-05 GYY4137 a H(2)S donor, attenuates ipsilateral epididymis injury in experimentally varicocele-induced rats via activation of the PI3K/Akt pathway Xia, Yu-qi Ning, Jin-zhuo Cheng, Fan Yu, Wei-min Rao, Ting Ruan, Yuan Yuan, Run Du, Yang Iran J Basic Med Sci Original Article OBJECTIVE(S): The current study was aimed to investigate the effect of morpholin-4-ium 4 methoxyphenyl (morpholino) phosphinodithioate (GYY4137) on ipsilateral epididymis injury in a rat model of experimental varicocele (VC). MATERIALS AND METHODS: Sixty Wistar rats were randomly assigned to sham, sham plus GYY4137, VC and VC plus GYY4137 groups. Sperm quality parameters, including sperm count, motility and viability were evaluated after 4 weeks. Histological changes were measured by hematoxylin and eosin staining between the groups. The oxidative stress levels were estimated by determining epididymal superoxide dismutase (SOD) and malondialdehyde (MDA). The apoptosis status and the expression of phosphatidylinositol 3′-OH kinase (PI3K)/Akt were analyzed by immunohistochemical analysis, western blot and RT-qPCR. RESULTS: VC resulted in the decrease of sperm parameters, significant histological damage and higher levels of oxidative stress and apoptosis. Compared to the VC group, GYY4137 markedly ameliorated these observed changes. In addition, treatment with GYY4137 obviously reduced the levels of caspase-3 and Bax and increased the levels of the phosphorylation of PI3K p85 and Akt. CONCLUSION: Our data demonstrated that GYY4137 may alleviate the sperm damage and epididymis injury in experimentally VC-induced rats by activation of the PI3K/Akt pathway. Mashhad University of Medical Sciences 2019-07 /pmc/articles/PMC7196355/ /pubmed/32373293 http://dx.doi.org/10.22038/ijbms.2019.30588.7372 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Xia, Yu-qi
Ning, Jin-zhuo
Cheng, Fan
Yu, Wei-min
Rao, Ting
Ruan, Yuan
Yuan, Run
Du, Yang
GYY4137 a H(2)S donor, attenuates ipsilateral epididymis injury in experimentally varicocele-induced rats via activation of the PI3K/Akt pathway
title GYY4137 a H(2)S donor, attenuates ipsilateral epididymis injury in experimentally varicocele-induced rats via activation of the PI3K/Akt pathway
title_full GYY4137 a H(2)S donor, attenuates ipsilateral epididymis injury in experimentally varicocele-induced rats via activation of the PI3K/Akt pathway
title_fullStr GYY4137 a H(2)S donor, attenuates ipsilateral epididymis injury in experimentally varicocele-induced rats via activation of the PI3K/Akt pathway
title_full_unstemmed GYY4137 a H(2)S donor, attenuates ipsilateral epididymis injury in experimentally varicocele-induced rats via activation of the PI3K/Akt pathway
title_short GYY4137 a H(2)S donor, attenuates ipsilateral epididymis injury in experimentally varicocele-induced rats via activation of the PI3K/Akt pathway
title_sort gyy4137 a h(2)s donor, attenuates ipsilateral epididymis injury in experimentally varicocele-induced rats via activation of the pi3k/akt pathway
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196355/
https://www.ncbi.nlm.nih.gov/pubmed/32373293
http://dx.doi.org/10.22038/ijbms.2019.30588.7372
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