Author:
Filipiuc Leontina-Elena,Creangă-Murariu Ioana,Tamba Bogdan-Ionel,Ababei Daniela-Carmen,Rusu Răzvan-Nicolae,Stanciu Gabriela-Dumitrița,Ștefanescu Raluca,Ciorpac Mitică,Szilagyi Andrei,Gogu Raluca,Filipiuc Silviu-Iulian,Tudorancea Ivona-Maria,Solcan Carmen,Alexa-Stratulat Teodora,Cumpăt Marinela-Carmen,Cojocaru Doina-Clementina,Bild Veronica
Abstract
AbstractChemotherapy-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.
Funder
Ministerul Cercetării, Inovării şi Digitalizării
Publisher
Springer Science and Business Media LLC