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Based on previous findings regarding the activities of GSH, we hypothesized that GSH would promote fat graft survival by suppressing ferroptosis

Its underlying mechanisms are multifaceted, encompassing genetic variations, environmental influences, cerebral artery constriction, abnormalities in monoamine neurotransmitters, oxidative stress, mitochondrial disturbances, the involvement of calcitonin gene-related peptide (CGRP), neurogenic inflammation, and broader neuroinflammation (6)

although the compounds are natural, they are not known to exist in nature and are derived from another protein (Bdis et al

Centrifuge at 750 g for 20 min at room temperature (see Note 3)