5 ESSENTIAL ELEMENTS FOR BLOCK PAIN RECEPTORS WITH PROLEVIATE

Acquiring discovered the palmitoylation motif of APLNR, we developed a brief substrate sequence to competitively inhibit the palmitoylation of endogenous APLNR. This aggressive peptide, which targets the APLNR palmitoylation website in combination with morphine, can inhibit the development of NCP, which include pain incidence, microglial activation