Abstract

Purpose: The aim of this study was to investigate how glutathione reductase (GR) loses its activity during cataract formation and whether it is possible to revive it back to the normal levels. Method: In this study, endogenous as well as synthetic reducing systems (GSH, TTase, DTT, captopril) and α-crystallin at different concentrations were incubated with the soluble fraction of human cataract lens protein. The activity of glutathione reductase with or without the reducing agents and α-crystallin was tested, and the difference in activity gained was calculated. Results: Five agents (GSH, DTT, TTase, captopril, α -low crystallin) were able to revive the activity of GR from human cataract lenses to different extents. Conclusion: This study shows that human lens GR activity was revived by different reducing agents as well as by a molecular chaperone (α -crystallin).

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