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GHK-Cu, first identified in 1973 from mammalian plasma, functions as a naturally occurring copper-peptide complex that influences approximately 31% of the human genome, resetting gene expression patterns to favor tissue repair while delivering bioavailable copper essential for enzymatic processes underlying collagen synthesis and antioxidant defense

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On the other hand, when GSH-depleted cells were treated with N-acetyl cysteine (NAC), cytotoxicity/apoptosis caused by ASA was attenuated with a significant recovery in oxidative stress, GSH homeostasis, DNA fragmentation and some of the mitochondrial functions