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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.
Afiliação
  • Shin JY; Ministry of Food and Drug Safety, Cheongju, Korea.; College of Veterinary Medicine, Chonnam National University, Gwangju, Korea.
  • Han JH; College of Veterinary Medicine, Chonnam National University, Gwangju, Korea.
  • Ko JW; College of Veterinary Medicine, Chonnam National University, Gwangju, Korea.
  • Park SH; College of Veterinary Medicine, Chonnam National University, Gwangju, Korea.
  • Shin NR; College of Veterinary Medicine, Chonnam National University, Gwangju, Korea.
  • Jung TY; College of Veterinary Medicine, Chonnam National University, Gwangju, Korea.
  • Kim HA; College of Veterinary Medicine, Chonnam National University, Gwangju, Korea.
  • Kim SH; Jeonbuk Department of Inhalation Research, Korea Institute of Toxicology, Jeongeup, Korea.
  • Shin IS; College of Veterinary Medicine, Chonnam National University, Gwangju, Korea.
  • Kim JC; College of Veterinary Medicine, Chonnam National University, Gwangju, Korea.
Lab Anim Res ; 32(4): 200-207, 2016 Dec.
Article em En | MEDLINE | ID: mdl-28053613
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 (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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article