Such an increase in the mRNA levels of the catalytic subunit of -GCS was paralleled by a greater mucosal synthetic GSH capacity determined from either cysteine or -glutamylcysteine used as the sulfur aminoacid in the presence of glycine and glutamate and ATP as described (Fernndez-Checa and Kaplowitz, 1990), indicating an increase in the activity of -GCS following TNBS+ethanol administration (not shown)
The CXCR4 receptor appears to be critically involved in many of these effects, particularly in regulating autophagy, IGF-1 abundance, Akt phosphorylation, and oxidative stress, as AMD3100 reversed these protective actions
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