Mezni Ali, Khazri Olfa, Jarnier Frédérique, Hardouin Julie, Limam Ferid, Jouenne Thierry, Aouani Ezzeddine, Cosette Pascal
Laboratoire des Substances Bioactives (LSBA), Centre de Biotechnologie de Borj Cedria, Hammam-Lif, Tunisie.
Université de Carthage, Faculté des Sciences de Bizerte, Zarzouna, Tunisie.
Dose Response. 2022 Nov 22;20(4):15593258221141585. doi: 10.1177/15593258221141585. eCollection 2022 Oct-Dec.
The liver is the organ by which the majority of substances are metabolized, including psychotropic drugs. Lithium (Li) used as drug for many neurological disorders such as bipolar disorders.
This study aims to assess lithium toxicity and to evaluate the hepatic-protective properties of a grape skin seed and extract (GSSE).
Twenty-four male Wistar rats were exposed for 30 days to either various lithium concentrations, GSSE alone, or lithium supplemented with GSSE. The proteomic analysis revealed alterations of liver protein profiles after lithium treatments that were successfully identified by mass spectrometry.
Lithium treatment induced an oxidative damage by the alteration of antioxidant enzymes activities such as superoxide dismutase, CAT, and Gpx. The regulated proteins are mainly involved in the respiratory electron transport chain, detoxification processes, ribosomal stress pathway, glycolysis, and cytoskeleton. Proteins were differentially expressed in a dose-dependent manner. Interestingly, GSSE reversed the situation and restored the level of liver proteins whose abundance was modified after lithium treatment, arguing for its protective activity.
Our data demonstrated the ability of proteomic analysis to underline the toxicity mechanisms of lithium in animal models. Based on these results, GSSE may be envisaged as a nutritional supplement to weaken the liver toxicity of lithium.
肝脏是大多数物质(包括精神药物)进行代谢的器官。锂(Li)被用作治疗多种神经疾病(如双相情感障碍)的药物。
本研究旨在评估锂的毒性,并评价葡萄皮籽提取物(GSSE)的肝脏保护特性。
将24只雄性Wistar大鼠分别暴露于不同锂浓度、单独的GSSE或锂与GSSE联合处理30天。蛋白质组学分析揭示了锂处理后肝脏蛋白质谱的变化,这些变化通过质谱成功鉴定。
锂处理通过改变超氧化物歧化酶、CAT和谷胱甘肽过氧化物酶等抗氧化酶的活性诱导氧化损伤。受调控的蛋白质主要参与呼吸电子传递链、解毒过程、核糖体应激途径、糖酵解和细胞骨架。蛋白质以剂量依赖的方式差异表达。有趣的是,GSSE扭转了这种情况,并恢复了锂处理后丰度发生改变的肝脏蛋白质水平,证明了其保护活性。
我们的数据证明了蛋白质组学分析能够揭示动物模型中锂的毒性机制。基于这些结果,GSSE可被设想为一种营养补充剂,以减轻锂对肝脏的毒性。