Lin Dongju, Wang Kai, Guo Xiucai, Gao Huiyuan, Peng Ying, Zheng Jiang
School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning, 110016, PR China.
School of Traditional Chinese Medicine, Shenyang Pharmaceutical University, Shenyang, Liaoning, 110016, PR China; Key Laboratory of Structure-Based Drug Design & Discovery of Ministry of Education, Shenyang Pharmaceutical University, Shenyang, Liaoning, 110016, PR China.
Toxicol Lett. 2016 Dec 15;264:20-28. doi: 10.1016/j.toxlet.2016.10.007. Epub 2016 Nov 2.
Furanoid 8-epidiosbulbin E acetate (EEA) is a major constituent of herbal medicine Dioscorea bulbifera L. (DB), a traditional herbal medicine widely used in Asian nations. Our early studies demonstrated that administration of EEA caused acute hepatotoxicity in mice and the observed toxicity required P450-mediated metabolic activation. Protein modification by reactive metabolites of EEA has been suggested to be an important mechanism of EEA-induced hepatotoxicity. The objectives of the present study were to investigate the interaction of the electrophilic reactive metabolites derived from EEA with lysine and cysteine residues of proteins and to define the correlation of protein adductions of EEA and the hepatotoxicity induced by EEA. EEA-derived cis-enedial was found to modify both lysine and cysteine residues of proteins. The observed modifications increased with the increase in doses administered in the animals. The formation of protein adductions derived from the reactive metabolites of EEA were potentiated by buthionine sulfoximine, but were attenuated by ketoconazole. This work facilitated better understanding of the mechanisms of toxic action of EEA.
呋喃型8-表薯蓣皂苷元醋酸酯(EEA)是中药黄独(DB)的主要成分,黄独是一种在亚洲国家广泛使用的传统草药。我们早期的研究表明,给予EEA会导致小鼠急性肝毒性,且观察到的毒性需要P450介导的代谢活化。EEA的活性代谢产物对蛋白质的修饰被认为是EEA诱导肝毒性的重要机制。本研究的目的是研究EEA衍生的亲电活性代谢产物与蛋白质的赖氨酸和半胱氨酸残基的相互作用,并确定EEA的蛋白质加合物与EEA诱导的肝毒性之间的相关性。发现EEA衍生的顺式烯二醛会修饰蛋白质的赖氨酸和半胱氨酸残基。观察到的修饰随着给予动物剂量的增加而增加。EEA活性代谢产物衍生的蛋白质加合物的形成被丁硫氨酸亚砜胺增强,但被酮康唑减弱。这项工作有助于更好地理解EEA的毒性作用机制。