We demonstrated that, in contrast to classical opioid receptors, ACKR3 isn't going to trigger classical G protein signaling and isn't modulated by the classical prescription or analgesic opioids, which include morphine, fentanyl, or buprenorphine, or by nonselective opioid antagonists including naloxone. As an alternative, we proven that LIH383, an https://rogerd889etj9.activablog.com/profile