Advanced Research and Development Center for Experimental Medicine (CEMEX), "Grigore T. Popa" University of Medicine and Pharmacy, University Street No. 16, 700115, Iasi, Romania.
Department of Pharmacology, Clinical Pharmacology and Algesiology, "Grigore T. Popa" University of Medicine and Pharmacy, University Street No. 16, 700115, Iasi, Romania.
Sci Rep. 2024 Jul 15;14(1):16242. doi: 10.1038/s41598-024-67154-y.
Chemotherapy-induced neuropathic pain (CINP), a condition with unmet treatment needs, affects over half of cancer patients treated with chemotherapeutics. Researchers have recently focused on the endocannabinoid system because of its critical role in regulating our bodies' most important functions, including pain. We used in vitro and in vivo methods to determine the toxicity profile of a synthetic cannabinoid, JWH-182, and whether it could be potentially effective for CINP alleviation. In vitro, we evaluated JWH-182 general toxicity, measuring fibroblast viability treated with various concentrations of compound, and its neuroprotection on dorsal root ganglion neurons treated with paclitaxel. In vivo, we performed an evaluation of acute and 28-day repeated dose toxicity in mice, with monitoring of health status and a complete histopathological examination. Finally, we evaluated the efficacy of JWH-182 on a CINP model in mice using specific pain assessment tests. JWH-182 has an acceptable toxicity profile, in both, in vitro and in vivo studies and it was able to significantly reduce pain perception in a CINP model in mice. However, the translation of these results to the clinic needs further investigation.
化疗诱导性神经病理性疼痛(CINP)是一种未满足治疗需求的病症,影响了超过一半接受化疗的癌症患者。由于内源性大麻素系统在调节我们身体最重要的功能(包括疼痛)方面起着关键作用,研究人员最近将注意力集中在该系统上。我们使用体外和体内方法来确定合成大麻素 JWH-182 的毒性概况,以及它是否可能对 CINP 缓解有效。在体外,我们评估了 JWH-182 的一般毒性,测量了用不同浓度化合物处理的成纤维细胞的活力,以及它对紫杉醇处理的背根神经节神经元的神经保护作用。在体内,我们在小鼠中进行了急性和 28 天重复剂量毒性的评估,监测了健康状况并进行了全面的组织病理学检查。最后,我们使用特定的疼痛评估测试在 CINP 模型小鼠中评估了 JWH-182 的疗效。JWH-182 在体外和体内研究中具有可接受的毒性概况,并且能够显著减轻 CINP 模型小鼠的疼痛感知。然而,将这些结果转化为临床应用需要进一步研究。