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As a key beneficial genus within the gut microbiota, Bifidobacterium contributes to gut homeostasis through the secretion of SCFAs and suppression of pathogenic bacterial proliferation [37, 38]

However, the pharmacokinetic characteristics, tissue bioaccumulation, and toxicity profiles of arsenic metabolites in vivo following oral administration of ATO have not yet been characterized

By activating the HGF/c-Met pathway and enhancing BDNF signaling, Dihexa supports true neuroplasticity and structural brain improvements that can persist beyond treatment duration

Ferroptosis, an iron-dependent form of RCD driven by GSH depletion and GPX4 inactivation, is potently accelerated by copper through multi-pronged mechanisms that converge on iron-dependent lipid peroxidation [61, 62]