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Previous research (78) has also revealed a broader range of functions for ChaC2 than previously understood

[2] Pharmacokinetic studies demonstrate rapid systemic distribution with peak plasma levels occurring within 30-60 minutes of intramuscular injection, followed by extensive hepatic storage and enterohepatic recycling

Since many harmful conditions are known to directly disrupt the GPx, inhibition of ferroptosis may represent a suitable therapeutic approach to improve hepatocyte cell death