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It is generally understood that GST enzymes function may complement phase I (cytochrome P450) biotransformation enzymes by mediating the conjugation of glutathione (GSH, tripeptide, -L- glutamyl-L-cysteinyl-glycine) to endogenous and exogenous substances, reducing toxicity and increasing solubility toward their excretion from cells [1]

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Modulatory Effects of Multi-species/Multi-strain Synbiotic and L-carnitine Concomitant Supplementation on Atherogenic-Indices, Body Composition, Visceral Obesity, and Appetite in Metabolically Healthy Women with Obesity: A Double-Blind Randomized Controlled Clinical Trial

methods of detecting lipid peroxidation include use of the thiobarbituric acid reactive substances (TBARS) assay, detection of isoprostanes or lipid peroxidation products directly by LC-MS/MS, oxidation of the C11-BODIPY fluorescent probe, and reactivity with antibodies that detect adducts formed by products of lipid peroxidation, such as with the anti-HNE FerAb antibody (Kobayashi et al., 2021), the HNEJ-1 antibody (Zheng et al., 2021), and the anti-MDA adduct 1F83 antibody (Yamada et al., 2001) (Figure 5)

Benefits are primarily related to reduced oxidative stress and potential accelerated recovery, not necessarily aesthetic gains