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      Reactive oxygen species involved in phenazine-methosulfate-induced rat lens opacification. An experimental model of cataract.

      Ophthalmic research
      Animals, Cataract, chemically induced, metabolism, pathology, Disease Models, Animal, Electron Spin Resonance Spectroscopy, Hydroxyl Radical, Lens, Crystalline, drug effects, Male, Methylphenazonium Methosulfate, Organ Culture Techniques, Rats, Rats, Wistar, Reactive Oxygen Species, toxicity, Sodium-Potassium-Exchanging ATPase, Superoxides, Water-Electrolyte Imbalance

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          Abstract

          The excised rat crystalline lens opacified when incubated aerobically with phenazine methosulfate, but no opacification was observed under anaerobic conditions. Morphological studies revealed development of opacification in the cortex. The opacification resembled that often seen in the early period of senile cataract as well as in naphthalene-induced and UV cataract. Both an increase in hydration and in electrolyte imbalance accompanied this opacification. Na,K-ATPase activity of the opacified lens was found to decrease. In order to investigate if activated oxygen is involved in these processes, we conducted an electron spin resonance study by means of a spin trapping technique. When the lens homogate was incubated with phenazine methosulfate, OH radicals were generated under aerobic but not under anaerobic conditions. Reduced pyridine nucleotides must be involved in the process, because the mixture of nicotinamide adenine dinucleotide phosphate [NAD(P)] and phenazine methosulfate did not generate OH radicals, but the mixture of NAD(P)H and phenazine methosulfate generates OH radicals, indicating that reduced phenazine methosulfate was involved in the OH radical generation. Probably, the generated OH radicals inactivated Na,K-ATPase residing in the epithelium of the lens, which eventually caused opacification of the lens. The present experiment system may be used for the elucidation of lens opacification (cataract) involved with reactive oxygen species.

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