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Conolidine’s analgesic results stem from its interaction with non-opioid pain pathways. In contrast to opioids, which bind to µ-opioid receptors from the central nervous system, conolidine modulates alternate molecular targets. A Science Advancements review found that conolidine interacts Using the atypical chemokine receptor ACKR3/CXCR7, which
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Whilst it is not known whether other unidentified interactions are taking place within the receptor that contribute to its results, the receptor plays a job like a detrimental down regulator of endogenous opiate levels by means of scavenging activity. This drug-receptor interaction offers a substitute for manipulation on the classical opiate pathwa