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The effect of an specific inducible NO synthase inhibitor, S-methylisothiourea hemisulfate on cisplatin-induced nephrotoxicity; gender-related differences
BACKGROUNDS: It has been previously demonstrated that the increase of nitric oxide (NO) level may promote cisplatin (CP)-induced nephrotoxicity. The aim of this study was to investigate the role of inducible NO synthase (iNOS) inhibitor to prevent CP-induced nephrotoxicity. MATERIALS AND METHODS: Fo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544122/ https://www.ncbi.nlm.nih.gov/pubmed/26322278 http://dx.doi.org/10.4103/2277-9175.161223 |
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author | Ghayyoomi, Mansooreh Soltani, Nepton Nematbakhsh, Mehdi Moslemi, Fatemeh Talebi, Ardeshir Shirdavani, Soheila Razmjoo, Farzaneh |
author_facet | Ghayyoomi, Mansooreh Soltani, Nepton Nematbakhsh, Mehdi Moslemi, Fatemeh Talebi, Ardeshir Shirdavani, Soheila Razmjoo, Farzaneh |
author_sort | Ghayyoomi, Mansooreh |
collection | PubMed |
description | BACKGROUNDS: It has been previously demonstrated that the increase of nitric oxide (NO) level may promote cisplatin (CP)-induced nephrotoxicity. The aim of this study was to investigate the role of inducible NO synthase (iNOS) inhibitor to prevent CP-induced nephrotoxicity. MATERIALS AND METHODS: Four groups of male and four groups of female rats were treated daily with vehicle, S-methylisothiourea hemisulfate (SMT) as a selective iNOS inhibitor (5 mg/kg/twice a day), CP (2.5 mg/kg/day), and CP + SMT for 6 days. Then, all animals were sacrificed and the serum levels of creatinine (Cr), blood urea nitrogen (BUN), nitrite, and malondialdehyde (MDA) were measured. The kidney was removed immediately for histopathological study. RESULTS: Our results showed that inhibition of iNOS by SMT could make different response in male and female animals. SMT therapy in male animals decreased serum BUN, Cr, nitrite, and MDA levels; and it also protected kidney against CP-induced nephrotoxicity. CONCLUSION: It is concluded that decrease in NO production by SMT has a beneficial effect on reducing CP-induced nephrotoxicity in male. However, such beneficial effect was not observed in female animals. |
format | Online Article Text |
id | pubmed-4544122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45441222015-08-28 The effect of an specific inducible NO synthase inhibitor, S-methylisothiourea hemisulfate on cisplatin-induced nephrotoxicity; gender-related differences Ghayyoomi, Mansooreh Soltani, Nepton Nematbakhsh, Mehdi Moslemi, Fatemeh Talebi, Ardeshir Shirdavani, Soheila Razmjoo, Farzaneh Adv Biomed Res Original Article BACKGROUNDS: It has been previously demonstrated that the increase of nitric oxide (NO) level may promote cisplatin (CP)-induced nephrotoxicity. The aim of this study was to investigate the role of inducible NO synthase (iNOS) inhibitor to prevent CP-induced nephrotoxicity. MATERIALS AND METHODS: Four groups of male and four groups of female rats were treated daily with vehicle, S-methylisothiourea hemisulfate (SMT) as a selective iNOS inhibitor (5 mg/kg/twice a day), CP (2.5 mg/kg/day), and CP + SMT for 6 days. Then, all animals were sacrificed and the serum levels of creatinine (Cr), blood urea nitrogen (BUN), nitrite, and malondialdehyde (MDA) were measured. The kidney was removed immediately for histopathological study. RESULTS: Our results showed that inhibition of iNOS by SMT could make different response in male and female animals. SMT therapy in male animals decreased serum BUN, Cr, nitrite, and MDA levels; and it also protected kidney against CP-induced nephrotoxicity. CONCLUSION: It is concluded that decrease in NO production by SMT has a beneficial effect on reducing CP-induced nephrotoxicity in male. However, such beneficial effect was not observed in female animals. Medknow Publications & Media Pvt Ltd 2015-07-20 /pmc/articles/PMC4544122/ /pubmed/26322278 http://dx.doi.org/10.4103/2277-9175.161223 Text en Copyright: © 2015 Ghayyoomi. http://creativecommons.org/licenses/by-nc-sa/3.0 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 credited. |
spellingShingle | Original Article Ghayyoomi, Mansooreh Soltani, Nepton Nematbakhsh, Mehdi Moslemi, Fatemeh Talebi, Ardeshir Shirdavani, Soheila Razmjoo, Farzaneh The effect of an specific inducible NO synthase inhibitor, S-methylisothiourea hemisulfate on cisplatin-induced nephrotoxicity; gender-related differences |
title | The effect of an specific inducible NO synthase inhibitor, S-methylisothiourea hemisulfate on cisplatin-induced nephrotoxicity; gender-related differences |
title_full | The effect of an specific inducible NO synthase inhibitor, S-methylisothiourea hemisulfate on cisplatin-induced nephrotoxicity; gender-related differences |
title_fullStr | The effect of an specific inducible NO synthase inhibitor, S-methylisothiourea hemisulfate on cisplatin-induced nephrotoxicity; gender-related differences |
title_full_unstemmed | The effect of an specific inducible NO synthase inhibitor, S-methylisothiourea hemisulfate on cisplatin-induced nephrotoxicity; gender-related differences |
title_short | The effect of an specific inducible NO synthase inhibitor, S-methylisothiourea hemisulfate on cisplatin-induced nephrotoxicity; gender-related differences |
title_sort | effect of an specific inducible no synthase inhibitor, s-methylisothiourea hemisulfate on cisplatin-induced nephrotoxicity; gender-related differences |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544122/ https://www.ncbi.nlm.nih.gov/pubmed/26322278 http://dx.doi.org/10.4103/2277-9175.161223 |
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