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Yangonin, one of the kavalactones isolated from Piper methysticum G. Forst, acts through cannabinoid 1 (CB1) receptors to induce an intrathecal anti-hyperalgesia.

Lok-Hi Chow, Pin-Chen Lin, Ying-Jie Chen, Yuan-Hao Chen, Eagle Yi-Kung Huang

Journal of ethnopharmacology October 28, 2024 DOI: 10.1016/j.jep.2024.118394 via PubMed

Summary

AI-generated from the abstract

Yangonin, a kavalactone from kava, reduced pain sensitivity and inflammation-induced pain in rats when injected into the spinal cord. These effects were blocked by a cannabinoid 1 (CB1) receptor antagonist, indicating yangonin acts through CB1 receptors. Yangonin did not affect nerve injury-induced pain. Kavain, another kavalactone, had no effect on any pain type tested.

Study at a glance

Characteristics Experimental study Peer reviewed
Population Male Sprague-Dawley rats
Interventions kavain yangonin
Dose 27.14 and 19.36 nmol/rat
Keywords Anti-hyperalgesia Kavain Kavalactones Yangonin
Citations 6
Key finding Yangonin exerts anti-nociceptive and anti-inflammatory hyperalgesic effects via CB1 receptors at the spinal level, while kavain shows no such effects.

Abstract

Piper methysticum G. Forst (Piperaceae) is traditionally consumed in Polynesian culture. The roots are used to produce an entheogenic drink and traditional medicine with sedative and anxiolytic properties. There is also evidence that it functions as a pain reliever. Kavalactones, its main active ingredients, exhibit psychoactive effects on the central nervous system. However, the active ingredients and pharmacological mechanisms underlying the analgesic effect of kavalactones are unclear. This study investigated the effects of kavain and yangonin on nociception, inflammatory hyperalgesia, and neuropathic mechanical allodynia at the spinal level. Male Sprague-Dawley rats were administered kavain and yangonin (27.14 and 19.36 nmol/rat) via intrathecal injection. Tail-flick tests were performed to evaluate the anti-nociceptive properties. The efficacy of kavain and yangonin on inflammatory hyperalgesia was examined using a plantar test in rats with carrageenan-induced paw inflammation. The von Frey test was used to assess mechanical allodynia induced by partial sciatic nerve ligation. Intrathecal injection of yangonin demonstrated a relatively potent anti-nociceptive effect and attenuated carrageenan-induced hyperalgesia. These effects were completely reversed by the co-administration of PF 514273, a cannabinoid 1 (CB1) receptor antagonist. However, yangonin did not affect mechanical allodynia at the spinal level. Kavain, another abundant kavalactone, did not affect nociception, hyperalgesia, or mechanical allodynia at the spinal level. Overall, our study demonstrated that yangonin exerts anti-nociception and anti-inflammatory hyperalgesia effects via CB1 receptors at the spinal level. We identified a single kavalactone, yangonin, extracted from kava as a promising treatment for pain.

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