a Third Company, Faculty of Naval Medicine , Second Military Medical University , Shanghai , P.R. China.
b Department of Pharmacy , The Fifth People's Hospital of Shanghai, School of Medicine, Fudan University , Shanghai , P.R. China.
Toxicol Mech Methods. 2017 Nov;27(9):687-696. doi: 10.1080/15376516.2017.1351017. Epub 2017 Jul 28.
Veratrum nigrum L. (VN) is a poisonous traditional Chinese medicine herb present since thousands of years in China. Clinical studies have shown that VN has the ability to cause hepatotoxicity, which severely limits its clinical use. The mechanism of its hepatotoxicity has not been fully elucidated. The purpose of this study was to develop and characterize a model of acute and chronic hepatotoxicity induced by Veratrum nigrum L. extract (VNE) to understand the mechanism of liver tissue metabolomics approach using on ultra-high-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UHPLC-Q-TOFMS). Mice were administered with VNE in the acute and chronic phases. Histopathologic inspections and biochemistry analysis disclosed severe liver damage after exposure to VNE. A partial least-squares discriminant analysis (PLS-DA) of the metabolomic profiles of rat liver tissues highlighted a number of metabolic disturbances induced by VNE, focusing on purine and pyrimidine metabolism, tryptophan metabolism, phospholipid metabolism, sphingolipid metabolism and fatty acid metabolism. These findings could well explain VNE-induced acute and chronic hepatotoxicity and reveal several potential biomarkers associated with this toxicity. This indicates that UHPLC-Q-TOFMS-based metabolomics approach demonstrated its feasibility and allowed a better understanding of VNE-induced liver toxicity dynamically.
藜芦(VN)是一种具有毒性的传统中药,在中国已有数千年的应用历史。临床研究表明,VN 具有引起肝毒性的能力,这严重限制了其在临床上的应用。其肝毒性的机制尚未完全阐明。本研究旨在建立和鉴定藜芦提取物(VNE)诱导的急性和慢性肝毒性模型,采用基于超高效液相色谱-四极杆飞行时间质谱联用(UHPLC-Q-TOFMS)的肝组织代谢组学方法来了解其作用机制。将 VNE 给予小鼠进行急性和慢性实验。组织病理学检查和生物化学分析显示,VNE 暴露后肝脏严重受损。对大鼠肝组织代谢组学图谱的偏最小二乘判别分析(PLS-DA)突出显示了 VNE 诱导的多种代谢紊乱,重点是嘌呤和嘧啶代谢、色氨酸代谢、磷脂代谢、鞘脂代谢和脂肪酸代谢。这些发现可以很好地解释 VNE 诱导的急性和慢性肝毒性,并揭示与这种毒性相关的一些潜在生物标志物。这表明基于 UHPLC-Q-TOFMS 的代谢组学方法具有可行性,并能动态地更好地了解 VNE 诱导的肝毒性。