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Finally, in vitro studies have shown the potential of NAC (1nM) to disassemble fibrils, protofibrils, oligomers and dimers of A molecules by blocking continuity in their oligomerization, a phenomenon mediated by the formation of hydrogen bridges between the A molecule and NAC, and by the stabilization of the neprilysin protease which is part of the catabolic equilibrium of the A peptide [70,71,72]

Its prominence reflects the depth of preclinical literature supporting its role in tissue-repair research

These approaches lack robust clinical trial data but reflect practical strategies used in clinical settings

In recent years, the role of different acyl-CoAs in the posttranslational acylation of protein lysine residues has acquired increasing attention (42)