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Supporting mitochondrial function through peptides like SS-31 while simultaneously promoting neurogenesis and reducing inflammation through other peptides represents a multi-target approach to conditions that have resisted single-target therapies for decades

One is that GSSG and GS-X produced in cardiomyocytes are pumped out by multidrug resistance protein 1 (MRP1), preventing GSSG or GS-X accumulation in cardiomyocytes [33, 34], and subsequently enter the -glutamyl cycle

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