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Diallyl disulfide attenuates acetaminophen-induced renal injury in rats
This study investigated the protective effects of diallyl disulfide (DADS) against acetaminophen (AAP)-induced acute renal injury in male rats. We also investigated the effects of DADS on kidney injury molecule-1 (KIM-1) and neutrophil gelatinase-associated lipocalin (NGAL), which are novel biomarke...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association for Laboratory Animal Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206226/ https://www.ncbi.nlm.nih.gov/pubmed/28053613 http://dx.doi.org/10.5625/lar.2016.32.4.200 |
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author | Shin, Jin-Young Han, Ji-Hee Ko, Je-Won Park, Sung-Hyeuk Shin, Na-Rae Jung, Tae-Yang Kim, Hyun-A Kim, Sung-Hwan Shin, In-Sik Kim, Jong-Choon |
author_facet | Shin, Jin-Young Han, Ji-Hee Ko, Je-Won Park, Sung-Hyeuk Shin, Na-Rae Jung, Tae-Yang Kim, Hyun-A Kim, Sung-Hwan Shin, In-Sik Kim, Jong-Choon |
author_sort | Shin, Jin-Young |
collection | PubMed |
description | This study investigated the protective effects of diallyl disulfide (DADS) against acetaminophen (AAP)-induced acute renal injury in male rats. We also investigated the effects of DADS on kidney injury molecule-1 (KIM-1) and neutrophil gelatinase-associated lipocalin (NGAL), which are novel biomarkers of nephrotoxicity in renal tissues, in response to AAP treatment. The following four experimental groups were evaluated: (1) vehicle control, (2) AAP (1,000 mg/kg), (3) AAP&DADS, and (4) DADS (50 mg/kg/day). AAP treatment caused acute kidney injury evidenced by increased serum blood urea nitrogen (BUN) levels and histopathological alterations. Additionally, Western blot and immunohistochemistry analysis showed increased expression of KIM-1 and NGAL proteins in renal tissues of AAP-treated rats. In contrast, DADS pretreatment significantly attenuated the AAP-induced nephrotoxic effects, including serum BUN level and expression of KIM-1 and NGAL proteins. Histopathological studies confirmed the renoprotective effect of DADS. The results suggest that DADS prevents AAP-induced acute nephrotoxicity, and that KIM-1 and NGAL may be useful biomarkers for the detection and monitoring of acute kidney injury associated with AAP exposure. |
format | Online Article Text |
id | pubmed-5206226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-52062262017-01-04 Diallyl disulfide attenuates acetaminophen-induced renal injury in rats Shin, Jin-Young Han, Ji-Hee Ko, Je-Won Park, Sung-Hyeuk Shin, Na-Rae Jung, Tae-Yang Kim, Hyun-A Kim, Sung-Hwan Shin, In-Sik Kim, Jong-Choon Lab Anim Res Original Article This study investigated the protective effects of diallyl disulfide (DADS) against acetaminophen (AAP)-induced acute renal injury in male rats. We also investigated the effects of DADS on kidney injury molecule-1 (KIM-1) and neutrophil gelatinase-associated lipocalin (NGAL), which are novel biomarkers of nephrotoxicity in renal tissues, in response to AAP treatment. The following four experimental groups were evaluated: (1) vehicle control, (2) AAP (1,000 mg/kg), (3) AAP&DADS, and (4) DADS (50 mg/kg/day). AAP treatment caused acute kidney injury evidenced by increased serum blood urea nitrogen (BUN) levels and histopathological alterations. Additionally, Western blot and immunohistochemistry analysis showed increased expression of KIM-1 and NGAL proteins in renal tissues of AAP-treated rats. In contrast, DADS pretreatment significantly attenuated the AAP-induced nephrotoxic effects, including serum BUN level and expression of KIM-1 and NGAL proteins. Histopathological studies confirmed the renoprotective effect of DADS. The results suggest that DADS prevents AAP-induced acute nephrotoxicity, and that KIM-1 and NGAL may be useful biomarkers for the detection and monitoring of acute kidney injury associated with AAP exposure. Korean Association for Laboratory Animal Science 2016-12 2016-12-23 /pmc/articles/PMC5206226/ /pubmed/28053613 http://dx.doi.org/10.5625/lar.2016.32.4.200 Text en Copyright © 2016 Korean Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Shin, Jin-Young Han, Ji-Hee Ko, Je-Won Park, Sung-Hyeuk Shin, Na-Rae Jung, Tae-Yang Kim, Hyun-A Kim, Sung-Hwan Shin, In-Sik Kim, Jong-Choon Diallyl disulfide attenuates acetaminophen-induced renal injury in rats |
title | Diallyl disulfide attenuates acetaminophen-induced renal injury in rats |
title_full | Diallyl disulfide attenuates acetaminophen-induced renal injury in rats |
title_fullStr | Diallyl disulfide attenuates acetaminophen-induced renal injury in rats |
title_full_unstemmed | Diallyl disulfide attenuates acetaminophen-induced renal injury in rats |
title_short | Diallyl disulfide attenuates acetaminophen-induced renal injury in rats |
title_sort | diallyl disulfide attenuates acetaminophen-induced renal injury in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206226/ https://www.ncbi.nlm.nih.gov/pubmed/28053613 http://dx.doi.org/10.5625/lar.2016.32.4.200 |
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