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Excessive oxidation of GDH leads to a decrease of glutamate in hepatocytes, which in turn reduces the production of N-acetylglutamate (NAG), an allosteric activator of carbamoyl phosphate synthetase (CPS)

T-AsiG-CPL exhibited good stability in PBS (10% serum) at 37 C for 24 h, as evidenced by the unchanged spherical morphology (Supplementary Fig

Redox-dependent changes in molecular properties of mitochondrial apoptosis-inducing factor

As a thiol-containing compound, GSH may regulate the redox sites of several ionotropic receptors and ion channels, altering their functional characteristics (Varga et al., 1997) through the glutamatergic receptors NMDA and -amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA)

Despite this short half-life, its effects persist due to its ability to stimulate long-lasting cellular responses