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Resveratrol decreases apoptosis and NLRP3 complex expressions in experimental varicocele rat model
OBJECTIVE(S): Varicocele is an abnormal dilation in the testicular vein, which can cause hypoxia, reactive oxygen species accumulation, elevation in testicular temperature, and promote apoptosis and increase proinflammatory cytokine production. According to the varicocele pathophysiology, it is poss...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811763/ https://www.ncbi.nlm.nih.gov/pubmed/29456821 http://dx.doi.org/10.22038/IJBMS.2018.21943.5625 |
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author | Hajipour, Elnaz Mashayekhi, Farideh Jalali Mosayebi, Ghasem Baazm, Maryam Zendedel, Adib |
author_facet | Hajipour, Elnaz Mashayekhi, Farideh Jalali Mosayebi, Ghasem Baazm, Maryam Zendedel, Adib |
author_sort | Hajipour, Elnaz |
collection | PubMed |
description | OBJECTIVE(S): Varicocele is an abnormal dilation in the testicular vein, which can cause hypoxia, reactive oxygen species accumulation, elevation in testicular temperature, and promote apoptosis and increase proinflammatory cytokine production. According to the varicocele pathophysiology, it is possible that a group of cytosolic receptors called nucleotide oligomerization domain (NOD)-like receptor family pyrin domain containing 3 (NLRP3) inflammasomes also involve in varicocele pathogenesis. Due to the important role of antioxidant in decreasing the testis tissue damage, in this study we investigated the protective effect of resveratrol (RES) on NLRP3 complex and apoptosis in experimental varicocele rats. MATERIALS AND METHODS: In this study, 40 male Wistar rats were randomly divided into 5 groups (8 rats in each group): Control, experimental left varicocele (ELV), ELV + ethanol, ELV + 20 mg/kg RES and ELV + 50 mg/kg RES. Varicocele was induced by partial ligation of the left renal vein. Three months after varicocele induction, RESwas orally administered to rats for 1 month. The expression levels of NLRP3, apoptosis associated speck-like protein (ASC), caspase-1, Bax and Bcl2 were analyzed using real time PCR. RESULTS: Our results showed that RESat both doses significantly (P≤ 0.05) decreased the gene expression levels of ASC, NLRP3, caspase-1 and Bax and increased Bcl2 gene expression at high dose. CONCLUSIONS: RESby reducing inflammatory factors and decreasing apoptosis might be used as adjuvant therapy to reduce varicocele complication. |
format | Online Article Text |
id | pubmed-5811763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-58117632018-02-16 Resveratrol decreases apoptosis and NLRP3 complex expressions in experimental varicocele rat model Hajipour, Elnaz Mashayekhi, Farideh Jalali Mosayebi, Ghasem Baazm, Maryam Zendedel, Adib Iran J Basic Med Sci Original Article OBJECTIVE(S): Varicocele is an abnormal dilation in the testicular vein, which can cause hypoxia, reactive oxygen species accumulation, elevation in testicular temperature, and promote apoptosis and increase proinflammatory cytokine production. According to the varicocele pathophysiology, it is possible that a group of cytosolic receptors called nucleotide oligomerization domain (NOD)-like receptor family pyrin domain containing 3 (NLRP3) inflammasomes also involve in varicocele pathogenesis. Due to the important role of antioxidant in decreasing the testis tissue damage, in this study we investigated the protective effect of resveratrol (RES) on NLRP3 complex and apoptosis in experimental varicocele rats. MATERIALS AND METHODS: In this study, 40 male Wistar rats were randomly divided into 5 groups (8 rats in each group): Control, experimental left varicocele (ELV), ELV + ethanol, ELV + 20 mg/kg RES and ELV + 50 mg/kg RES. Varicocele was induced by partial ligation of the left renal vein. Three months after varicocele induction, RESwas orally administered to rats for 1 month. The expression levels of NLRP3, apoptosis associated speck-like protein (ASC), caspase-1, Bax and Bcl2 were analyzed using real time PCR. RESULTS: Our results showed that RESat both doses significantly (P≤ 0.05) decreased the gene expression levels of ASC, NLRP3, caspase-1 and Bax and increased Bcl2 gene expression at high dose. CONCLUSIONS: RESby reducing inflammatory factors and decreasing apoptosis might be used as adjuvant therapy to reduce varicocele complication. Mashhad University of Medical Sciences 2018-02 /pmc/articles/PMC5811763/ /pubmed/29456821 http://dx.doi.org/10.22038/IJBMS.2018.21943.5625 Text en Copyright: © Iranian Journal of Basic Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Hajipour, Elnaz Mashayekhi, Farideh Jalali Mosayebi, Ghasem Baazm, Maryam Zendedel, Adib Resveratrol decreases apoptosis and NLRP3 complex expressions in experimental varicocele rat model |
title | Resveratrol decreases apoptosis and NLRP3 complex expressions in experimental varicocele rat model |
title_full | Resveratrol decreases apoptosis and NLRP3 complex expressions in experimental varicocele rat model |
title_fullStr | Resveratrol decreases apoptosis and NLRP3 complex expressions in experimental varicocele rat model |
title_full_unstemmed | Resveratrol decreases apoptosis and NLRP3 complex expressions in experimental varicocele rat model |
title_short | Resveratrol decreases apoptosis and NLRP3 complex expressions in experimental varicocele rat model |
title_sort | resveratrol decreases apoptosis and nlrp3 complex expressions in experimental varicocele rat model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811763/ https://www.ncbi.nlm.nih.gov/pubmed/29456821 http://dx.doi.org/10.22038/IJBMS.2018.21943.5625 |
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