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Glutathione depletion has been observed in various liver diseases, including fatty liver disease, viral hepatitis, and cirrhosis

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One hypothesis is that we observed a greater induction of NRF2 through liver-specific Gclc deletion as compared to KEAP1 inhibition with CDDO-me because CDDO-me is a weaker inhibitor of NRF2-KEAP1 interaction compared to the ROS generated following GSH depletion

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