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Y.SuY.ShiM
The most significant marker, considered a gold standard, was F2-isoprostane and this was significantly more reduced by oral Acetylglutathione than with the IV glutathione.[11],[12] Oral S-Acetyl Glutathione, dosed 200mg daily for 7 days, AM IV 1400mg, single dose Serum and urine tested after 1 week of administration N=6, (4 female, 2 male, average age 45) Markers chosen are measures of Antioxidants F2-Isoprostane is the Gold Standard of oxidative stress markers Conclusion: Oral S-A GSH compares favourably to a one-time, equivalent dose of IV administered Glutathione GSH : Blood levels are lower in the A-GSH group as compared to the IV group because the A-GSH is being taken up by the cell.[13] This is substantiated by the following markers: F2-Iso : (F2- isoprostane ) measurement of redox status and oxidative stress
Key effects documented in rodent models include: Altered expression of major GABA-A receptor subunit genes, including GABRB3, GABRE, and GABRQ Regulation of ion channels involved in GABA transport Modulation of dopamine receptor subtypes (DRD3, DRD5) and serotonin receptor genes simultaneously Changes in HCRT (hypocretin/orexin) gene expression, which may explain the absence of sedative effects observed with classical benzodiazepines Enkephalin Degradation Inhibition Selank, along with the closely related peptide Semax, has been found to inhibit aminopeptidase N (APN) and dipeptidyl peptidase IV (DPP-IV), enzymes responsible for the degradation of enkephalins and other endogenous regulatory peptides[3]
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2024;11:e2406080
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