Accordingly, both APR and GCL in the primary metabolic pathway are activated upon oxidation whereas the activity of enzymes that are part of the secondary pathway, APK and SAL1, is attenuated
Within the loop of Henle approximately 20% of the Ca 2+ in the glomerular filtrate is reabsorbed, all of which occurs in the TAL
Class 1 ferroptosis inducers, including erastin, imidazole ketone erastin, sulfasalazine, sorafenib, and HG106, directly inhibit xCT activity [92,93] and induce ferroptosis by preventing cystine uptake and depleting cysteine or GSH, thereby inducing lipid peroxidation and cell death [15,49]
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