카나비노이드 수용체 활성화 및 TRPV1 억제를 통한 arachidonoyl-serotonin (AA-5-HT)의 진통 효과

Abstract

Pain is a noxious sensation caused by tissue damage, which can severely interfere with a person’s quality oflife. Although numerous analgesics are available for eradicating pain, there remain limitations in terms of safety andefficacy. This review focuses on arachidonoyl-serotonin (AA-5-HT) − an endogenous lipid with a putative antinociceptiveeffect. After detailed investigation, previous studies have revealed that AA-5-HT can stimulate the cannabinoid system,which results in the inhibition of pain sensation. Moreover, AA-5-HT can inhibit the action of TRPV1, which is a nonselectivecation channel that mediates pain signals in the nervous system. This dual effect makes AA-5-HT a potentiallysafe and potent analgesic. This review summarizes the roles of the cannabinoid system and TRPV1 in pain sensation, andthe function of AA-5-HT in pain modulation.