Stankova 2010 Toxicol In Vitro

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StaňkovÑ P, Kučera O, LotkovÑ H, Rouőar T, Endlicher R, CervinkovÑ Z (2010) The toxic effect of thioacetamide on rat liver in vitro. Toxicol In Vitro 24:2097-2103.

Β» PMID: 20600801

Stankova Pavla, Kucera Otto, Lotkova Halka, Rousar Tomas, Endlicher Rene, Cervinkova Zuzana (2010) Toxicol In Vitro

Abstract: Thioacetamide (TAA) is a hepatotoxin frequently used for experimental purposes which produces centrilobular necrosis after a single dose administration. In spite of the fact that oxidative stress seems to play a very important role in the mechanism of TAA-induced injury, the effect of TAA on hepatocytes in primary culture with respect to the influence on mitochondria has yet to be verified. Hepatocytes were incubated for 24h in a medium containing TAA (0-70 mmol/l). Glutathione content (GSH/GSSG), reactive oxygen species and malondialdehyde formation were assessed as markers of cell redox state. Toxicity was determined by lactate dehydrogenase leakage and WST-1 assay. The functional capacity of hepatocytes was evaluated from albumin and urea production. Mitochondrial metabolism was assessed by measuring mitochondrial membrane potential and oxygen consumption. Our results show that a profound decrease in the GSH level in hepatocytes precedes a sharp rise in endogenous ROS production. ROS production correlates with an increase in lipoperoxidation. Mitochondria are affected by TAA secondarily as a consequence of oxidative stress. Oxidation of the NADH-dependent substrates of respiratory Complex I is significantly more sensitive to the toxic action of TAA than oxidation of the flavoprotein-dependent substrate of Complex II. Mitochondria can also maintain their membrane potential better when they utilize succinate as a respiratory substrate. It appears that GSH should be depleted below a certain critical level in order to cause a marked increase in lipid peroxidation. Mitochondrial injury can then occur and cell death develops. β€’ Keywords: Hepatotoxicity

β€’ O2k-Network Lab: CZ Hradec Kralove Cervinkova Z, CZ Pardubice Rousar T


Stress:Oxidative stress;RONS 

Tissue;cell: Liver  Preparation: Permeabilized cells  Enzyme: Complex I, Complex II;succinate dehydrogenase  Regulation: mt-Membrane potential, Fatty acid 

Pathway: N, S  HRR: Oxygraph-2k 

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