We demonstrated that, in distinction to classical opioid receptors, ACKR3 does not result in classical G protein signaling and isn't modulated by the classical prescription or analgesic opioids, such as morphine, fentanyl, or buprenorphine, or by nonselective opioid antagonists such as naloxone. Alternatively, we established that LIH383, an ACKR3-selective https://juvenaly381yyd8.qodsblog.com/profile