Diallyl disulfide attenuates acetaminophen-induced renal injury in rats

Abstract 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 (NCAL), which are novel...

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Main Authors: Jin-Young Shin, Ji-Hee Han, Je-Won Ko, Sung-Hyeuk Park, Na-Rae Shin, Tae-Yang Jung, Hyun-A Kim, Sung-Hwan Kim, In-Sik Shin, Jong-Choon Kim
Format: Article
Language:English
Published: BMC 2016-12-01
Series:Laboratory Animal Research
Subjects:
Online Access:http://link.springer.com/article/10.5625/lar.2016.32.4.200
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author Jin-Young Shin
Ji-Hee Han
Je-Won Ko
Sung-Hyeuk Park
Na-Rae Shin
Tae-Yang Jung
Hyun-A Kim
Sung-Hwan Kim
In-Sik Shin
Jong-Choon Kim
author_facet Jin-Young Shin
Ji-Hee Han
Je-Won Ko
Sung-Hyeuk Park
Na-Rae Shin
Tae-Yang Jung
Hyun-A Kim
Sung-Hwan Kim
In-Sik Shin
Jong-Choon Kim
author_sort Jin-Young Shin
collection DOAJ
description Abstract 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 (NCAL), 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 NCAL 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 NCAL proteins. Histopathological studies confirmed the renoprotective effect of DADS. The results suggest that DADS prevents AAP-induced acute nephrotoxicity, and that KIM-1 and NCAL may be useful biomarkers for the detection and monitoring of acute kidney injury associated with AAP exposure.
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spelling doaj.art-0e16714d8fa542fdb800af453658ef492022-12-22T01:14:37ZengBMCLaboratory Animal Research2233-76602016-12-0132420020710.5625/lar.2016.32.4.200Diallyl disulfide attenuates acetaminophen-induced renal injury in ratsJin-Young Shin0Ji-Hee Han1Je-Won Ko2Sung-Hyeuk Park3Na-Rae Shin4Tae-Yang Jung5Hyun-A Kim6Sung-Hwan Kim7In-Sik Shin8Jong-Choon Kim9Ministry of Food and Drug SafetyCollege of Veterinary Medicine, Chonnam National UniversityCollege of Veterinary Medicine, Chonnam National UniversityCollege of Veterinary Medicine, Chonnam National UniversityCollege of Veterinary Medicine, Chonnam National UniversityCollege of Veterinary Medicine, Chonnam National UniversityCollege of Veterinary Medicine, Chonnam National UniversityJeonbuk Department of Inhalation Research, Korea Institute of ToxicologyCollege of Veterinary Medicine, Chonnam National UniversityCollege of Veterinary Medicine, Chonnam National UniversityAbstract 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 (NCAL), 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 NCAL 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 NCAL proteins. Histopathological studies confirmed the renoprotective effect of DADS. The results suggest that DADS prevents AAP-induced acute nephrotoxicity, and that KIM-1 and NCAL may be useful biomarkers for the detection and monitoring of acute kidney injury associated with AAP exposure.http://link.springer.com/article/10.5625/lar.2016.32.4.200AcetaminophennephrotoxicityKIM-1NCALdiallyl disulfideprotective effect
spellingShingle Jin-Young Shin
Ji-Hee Han
Je-Won Ko
Sung-Hyeuk Park
Na-Rae Shin
Tae-Yang Jung
Hyun-A Kim
Sung-Hwan Kim
In-Sik Shin
Jong-Choon Kim
Diallyl disulfide attenuates acetaminophen-induced renal injury in rats
Laboratory Animal Research
Acetaminophen
nephrotoxicity
KIM-1
NCAL
diallyl disulfide
protective effect
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 Acetaminophen
nephrotoxicity
KIM-1
NCAL
diallyl disulfide
protective effect
url http://link.springer.com/article/10.5625/lar.2016.32.4.200
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