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When consumed as a standard powder or tablet, the fragile tripeptide structure is rapidly degraded by gastric enzymes (such as gamma-glutamyltransferase) and undergoes aggressive first-pass hepatic metabolism, reducing the amount of GSH in the blood [2]

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Collectively, these studies, ranging from molecular mechanisms to translational applications, systematically establish ferroptosis as a central link connecting metabolic disorders, oxidative stress, and structural damage to renal tubule, thereby providing a new theoretical basis and intervention targets for DKD diagnosis and therapy

reduce the occurrence of age-related neurodegenerative diseases such as Alzheimers disease (AD) and Parkinsons disease (Son et al., 2012)