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Ameliorative effects of rutin against cisplatin-induced reproductive toxicity in male rats
BACKGROUND: Cisplatin (CP) or cis-diammine dichloroplatinum (II) is a platinum based standard antineoplastic drug which is used against variety of solid tumors and neoplasms. The present study aimed to evaluate the shielding effects of rutin against CP induced testicular toxicity in rats. METHODS: 2...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249881/ https://www.ncbi.nlm.nih.gov/pubmed/30463555 http://dx.doi.org/10.1186/s12894-018-0421-9 |
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author | Jahan, Sarwat Munawar, Asma Razak, Suhail Anam, Sara Ain, Qurat Ul Ullah, Hizb Afsar, Tayyaba Abulmeaty, Mahmoud Almajwal, Ali |
author_facet | Jahan, Sarwat Munawar, Asma Razak, Suhail Anam, Sara Ain, Qurat Ul Ullah, Hizb Afsar, Tayyaba Abulmeaty, Mahmoud Almajwal, Ali |
author_sort | Jahan, Sarwat |
collection | PubMed |
description | BACKGROUND: Cisplatin (CP) or cis-diammine dichloroplatinum (II) is a platinum based standard antineoplastic drug which is used against variety of solid tumors and neoplasms. The present study aimed to evaluate the shielding effects of rutin against CP induced testicular toxicity in rats. METHODS: 28 male rats were divided into four groups. First group was given saline orally while second group received intra-peritoneal (i.p) injection of cisplatin (7 mg/kg) on day first and received saline for next 13 days. Third group received i.p injection of cisplatin at day one and treated with rutin (75 mg/kg) orally for next 13 days. Fourth group was treated with rutin orally for 13 days. Animals were sacrificed on 14th day and reproductive organs were analyzed for various parameters. RESULTS: Cisplatin treatment resulted in a significant decrease in daily sperm production, decrease in head length and % DNA in head, reduction of epithelial cell height, tubular diameter, reduction of the number of spermatogonia, spermatocytes and spermatids, increase in the thiobarbituric acid reactive substances (TBARS) and oxidative stress in testicular tissues, and change of the intra-testicular testosterone concentrations. Rutin co-treatment resulted in reversing cisplatin effect on DNA damage, sperm count, histological and biochemical parameters. CONCLUSION: These results indicated that rutin co-treatment could ameliorate cisplatin-induced reproductive toxicity in male rats. |
format | Online Article Text |
id | pubmed-6249881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62498812018-11-26 Ameliorative effects of rutin against cisplatin-induced reproductive toxicity in male rats Jahan, Sarwat Munawar, Asma Razak, Suhail Anam, Sara Ain, Qurat Ul Ullah, Hizb Afsar, Tayyaba Abulmeaty, Mahmoud Almajwal, Ali BMC Urol Research Article BACKGROUND: Cisplatin (CP) or cis-diammine dichloroplatinum (II) is a platinum based standard antineoplastic drug which is used against variety of solid tumors and neoplasms. The present study aimed to evaluate the shielding effects of rutin against CP induced testicular toxicity in rats. METHODS: 28 male rats were divided into four groups. First group was given saline orally while second group received intra-peritoneal (i.p) injection of cisplatin (7 mg/kg) on day first and received saline for next 13 days. Third group received i.p injection of cisplatin at day one and treated with rutin (75 mg/kg) orally for next 13 days. Fourth group was treated with rutin orally for 13 days. Animals were sacrificed on 14th day and reproductive organs were analyzed for various parameters. RESULTS: Cisplatin treatment resulted in a significant decrease in daily sperm production, decrease in head length and % DNA in head, reduction of epithelial cell height, tubular diameter, reduction of the number of spermatogonia, spermatocytes and spermatids, increase in the thiobarbituric acid reactive substances (TBARS) and oxidative stress in testicular tissues, and change of the intra-testicular testosterone concentrations. Rutin co-treatment resulted in reversing cisplatin effect on DNA damage, sperm count, histological and biochemical parameters. CONCLUSION: These results indicated that rutin co-treatment could ameliorate cisplatin-induced reproductive toxicity in male rats. BioMed Central 2018-11-21 /pmc/articles/PMC6249881/ /pubmed/30463555 http://dx.doi.org/10.1186/s12894-018-0421-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Jahan, Sarwat Munawar, Asma Razak, Suhail Anam, Sara Ain, Qurat Ul Ullah, Hizb Afsar, Tayyaba Abulmeaty, Mahmoud Almajwal, Ali Ameliorative effects of rutin against cisplatin-induced reproductive toxicity in male rats |
title | Ameliorative effects of rutin against cisplatin-induced reproductive toxicity in male rats |
title_full | Ameliorative effects of rutin against cisplatin-induced reproductive toxicity in male rats |
title_fullStr | Ameliorative effects of rutin against cisplatin-induced reproductive toxicity in male rats |
title_full_unstemmed | Ameliorative effects of rutin against cisplatin-induced reproductive toxicity in male rats |
title_short | Ameliorative effects of rutin against cisplatin-induced reproductive toxicity in male rats |
title_sort | ameliorative effects of rutin against cisplatin-induced reproductive toxicity in male rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249881/ https://www.ncbi.nlm.nih.gov/pubmed/30463555 http://dx.doi.org/10.1186/s12894-018-0421-9 |
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