Obtaining identified the palmitoylation motif of APLNR, we designed a brief substrate sequence to competitively inhibit the palmitoylation of endogenous APLNR. This aggressive peptide, which targets the APLNR palmitoylation internet site together with morphine, can inhibit the development of NCP, together with pain incidence, microglial activation, and inflammatory aspect https://whyshouldiuseconolidine78653.blogocial.com/fascination-about-block-pain-receptors-with-proleviate-62828598