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Non‐cholinergic Toxicity of Organophosphates in Mammals: Interaction of Ethaphos with Mitochondrial Functions
Author(s) -
Holmuhamedov E. L.,
Kholmoukhamedova G. L.,
Baimuradov T. B.
Publication year - 1996
Publication title -
journal of applied toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.784
H-Index - 87
eISSN - 1099-1263
pISSN - 0260-437X
DOI - 10.1002/(sici)1099-1263(199611)16:6<475::aid-jat376>3.0.co;2-s
Subject(s) - mitochondrion , oxidative phosphorylation , biochemistry , respiratory chain , cytosol , inner mitochondrial membrane , membrane potential , atpase , toxicity , respiration , cellular respiration , chemistry , metabolism , biology , enzyme , botany , organic chemistry
The effect of the organophosphorus insecticide O ‐ethyl‐ S ‐propyl‐2, 4‐dichlorophenylphosphorothioate (ethaphos) on mitochondrial functions was studied. It was shown that ethaphos interacts with mitchondrial oxidative metabolism and inhibits oxidation of succinate, α‐glycerophosphate and pyruvate+malate at concentrations of 100, 75 and 50 μg mg −1 mitochondrial protein, respectively. Mitochondria treated with ethaphos show no changes in the inner membrane permeability and activity of cytochromes of the respiratory chain. Ethaphos has no inhibitory effect on the activity of mitochondrial ATPase. Addition of the electron donor pair (ascorbic acid + N , N , N ′, N ′‐tetramethyl‐ p ‐phenylenediamine) to ethaphos‐treated mitochondria restored the respiration and membrane potential. The membrane potential also can be re‐established in poisoned mitochondria by the addition of exogenous ATP. Based on the data obtained we show that mitochondrial dysfunctions induced by ethaphos can be partially eliminated and mitochondrial functions can be restored using artificial electron donors and/or through increasing the cytosolic ATP level.