Porceddu 2018 Methods Pharmacol Toxicol

From Bioblast
Jump to: navigation, search
Publications in the MiPMap
Porceddu M, Buron N, Rustin P, Fromenty B, Borgne-Sanchez A (2018) In vitro assessment of mitochondrial toxicity to predict drug-induced liver injury. Methods Pharmacol Toxicol Drug-Induced Liver Toxicity:283-300.

» [1]

Porceddu M, Buron N, Rustin P, Fromenty B, Borgne-Sanchez A (2018) Methods Pharmacol Toxicol

Abstract: Mitochondrial liability of drugs and other xenobiotics is a major issue for patients because such toxicity can damage different tissues and organs such as liver, heart, and muscle. Drug-induced mitochondrial toxicity is also a major concern for pharmaceutical industries. Indeed, it is now acknowledged that such mechanism of toxicity can induce severe, and sometimes fatal, liver injury which can lead to the interruption of clinical trials, or drug withdrawal after marketing, such as in the case of troglitazone. Therefore, drug-induced mitochondrial dysfunction is increasingly sought after by pharmaceutical companies by using reliable in vitro assays in order to discard potential mitochondrion-toxic drugs during drug discovery stage. This chapter presents the in vitro methods used to identify potential mitochondrion-toxic drugs. To this end, different types of biological materials are used such as isolated mouse liver mitochondria and the human hepatic HepaRG® cell line, which expresses the main enzymes and transcription factors involved in drug metabolism. The in vitro method we discussed allows to investigate several key mitochondrial parameters such as oxygen consumption, transmembrane potential, respiratory chain complex activities, and mtDNA levels. These investigations are able to detect not only direct and acute mitochondrial alterations due to parent drugs but also indirect and chronic mitochondrial liability that can be induced by secondary metabolites. Hence, it could be used to detect potential drug-induced mitochondrial liability and to understand the involved mechanisms.

Keywords: DILI, Drug-induced liver injury, Hepatocytes, Hepatotoxicity, Liver, Mitochondria, Mitochondrial toxicity, Oxidative stress, Respiratory chain, Transmembrane potential Bioblast editor: Kandolf G

Labels: MiParea: Respiration, mt-Medicine, Pharmacology;toxicology 

Tissue;cell: Liver 

HRR: Oxygraph-2k