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Exploration in the cascade working mechanisms of liver injury induced by total saponins extracted from Rhizoma Dioscorea bulbifera.
Yang, Fan; Liang, Yuqiong; Xu, Li; Ji, Leilei; Yao, Nan; Liu, Ruonan; Shi, Le; Liang, Tao.
Afiliação
  • Yang F; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, PR China.
  • Liang Y; Experiment Teaching Center, Faculty of Chinese Medicine Science, Guangxi University of Chinese Medicine, Nanning 530222, Guangxi Province, PR China.
  • Xu L; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, PR China.
  • Ji L; Center for Drug Safety Evaluation and Research, Nanjing University of Chinese Medicine, Nanjing 210023, PR China.
  • Yao N; Affiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing 210028, Jiangsu Province, PR China; Laboratory of Translational Medicine, Jiangsu Province Academy of Traditional Chinese Medicine, Nanjing 210028, Jiangsu Province, PR China.
  • Liu R; Department of Science and Technology, Nanjing University of Chinese Medicine, Nanjing 210023, PR China.
  • Shi L; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, PR China. Electronic address: shilehappy@163.com.
  • Liang T; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, PR China.
Biomed Pharmacother ; 83: 1048-1056, 2016 Oct.
Article em En | MEDLINE | ID: mdl-27544548
ABSTRACT
Rhizoma Dioscorea bulbifera, the tuber of Dioscorea bulbifera L., has been used to treat various diseases. However, the clinical application has been limited for its hepatotoxicity. In this study, we explored the cascade working mechanisms of time-dependent hepatotoxicity induced by total saponins extracted from Rhizoma Dioscorea bulbifera (TSRD). Animals were orally administered with TSRD for indicated time period. The adverse effects were determined by histopathology and biochemistry. Similar hepatic index was analyzed in L-O2 cells exposed to dioscin for different durations. We found that TSRD could initially cause cell damage and cholestasis in rats. With the treatment going on, oxidative stress injury and up-regulation of Cytochromes P450 (CYPs) were observed both in vitro and in vivo. Eventually, TSRD induced mitochondrial permeability results in apoptosis or necrosis. Taken together, we provided evidence for the time-dependent hepatotoxicity of TSRD and created a 3-step injury model to clarify its cascade working mechanisms.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saponinas / Transdução de Sinais / Dioscorea / Rizoma / Fígado Limite: Animals / Female / Humans / Male Idioma: En Revista: Biomed Pharmacother Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saponinas / Transdução de Sinais / Dioscorea / Rizoma / Fígado Limite: Animals / Female / Humans / Male Idioma: En Revista: Biomed Pharmacother Ano de publicação: 2016 Tipo de documento: Article