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1 November 2009 Cyclosporin A Inhibits UV-Radiation-Induced Membrane Damage but is Unable to Inhibit Carboxyatractyloside-Induced Permeability Transition
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Abstract

This work was undertaken to gain further information on the chemical characteristics of the membrane entity involved in the formation of the nonspecific pore. Mitochondria were subjected to oxidative stress by exposure to UV radiation. The results indicate that ultraviolet C radiation induces structural modifications in the adenine nucleotide translocase that lead to membrane permeability transition. Membrane leakage was assessed by measuring mitochondrial Ca2 transport, the transmembrane electric gradient, and mitochondrial swelling. UV-irradiated mitochondria were unable to retain matrix Ca2 or to maintain a high level of membrane potential when Ca2 was added; furthermore, UV-irradiated mitochondria underwent large amplitude swelling. Release of cytochrome c and formation of malondialdehyde, owing to lipid peroxidation, were also seen. Structural modifications of the translocase were revealed by an increase in the binding of the fluorescent probe eosin-5-maleimide to thiol residues of the ADP/ATP carrier. These modifications, taken together with findings indicating that cyclosporin resulted unable to inhibit carboxyatractyloside-induced permeability transition, prompted us to conclude that the translocase could constitute the nonspecific pore or at least be an important modulator of it.

Noemí García, Cecilia Zazueta, Mohammed El-Hafidi, Natalia Pavón, Eduardo Martínez-Abundis, Luz Hernández-Esquivel, and Edmundo Chávez "Cyclosporin A Inhibits UV-Radiation-Induced Membrane Damage but is Unable to Inhibit Carboxyatractyloside-Induced Permeability Transition," Radiation Research 172(5), 575-583, (1 November 2009). https://doi.org/10.1667/RR1799.1
Received: 22 March 2009; Accepted: 1 July 2009; Published: 1 November 2009
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