We demonstrated that, in contrast to classical opioid receptors, ACKR3 does not set off classical G protein signaling and is not modulated through the classical prescription or analgesic opioids, which include morphine, fentanyl, or buprenorphine, or by nonselective opioid antagonists which include naloxone. Rather, we recognized that LIH383, an https://baltasarr282hns2.wikienlightenment.com/user