Soriano Delia, Brumovsky Pablo Rodolfo, Villar Marcelo José, Coronel María Florencia
Laboratorio de Dolor en Cáncer, Instituto de Investigaciones en Medicina Traslacional CONICET - Universidad Austral, Av. Pte. Perón 1500, B1629AHJ, Pilar, Provincia de Buenos Aires, Buenos Aires, Argentina.
Facultad de Ciencias Biomédicas, Universidad Austral, Av. Pte. Perón 1500, B1629AHJ, Pilar, Buenos Aires, Argentina.
Psychopharmacology (Berl). 2025 Mar 31. doi: 10.1007/s00213-025-06778-y.
Paclitaxel-induced neuropathy stands out as the primary, dose-limiting side effect of this extensively used chemotherapy agent. Prolonged hypersensitivity and pain represent the most severe clinical manifestations. Effective preventive and therapeutic strategies are currently lacking.
Our study aimed to assess the impact of early oral administration of pharmaceutical-grade formulations containing the phytocannabinoids THC and CBD in a rat model of paclitaxel-induced neuropathy.
The experimental design involved the co-administration of paclitaxel and cannabinoid formulations with different THC to CBD ratios (THC:CBD 1:1 and THC:CBD 1:20) to adult male rats. Mechanical and thermal sensitivity, locomotor activity, vertical exploratory behaviors, anxiety-related parameters, weight gain, food and water consumption, and liver functionality were assessed.
Daily administration of THC:CBD 1:1 successfully prevented paclitaxel-induced cold allodynia, while THC:CBD 1:20 effectively prevented both thermal and mechanical hypersensitivities. Additionally, THC:CBD 1:1 formulation restored rearing behavior, significantly reduced by paclitaxel. Conversely, neither cannabinoid formulation was able to counteract paclitaxel-induced hypo-locomotion, reduced vertical exploratory activity, increased anxiety-like behaviors, attenuated weight gain, or decreased food and water intakes. However, the formulations employed did not induce further alterations or toxicity in animals receiving paclitaxel, and no signs of liver damage were detected.
Our results suggest a differential therapeutic effect of two THC:CBD formulations on pain-related behaviors and spontaneous activities, particularly in the context of peripheral neuropathy. These formulations represent a promising therapeutic strategy not only to managing pain but also for enhancing daily activities and improving the quality of life for cancer patients.
紫杉醇引起的神经病变是这种广泛使用的化疗药物的主要剂量限制性副作用。长期超敏反应和疼痛是最严重的临床表现。目前缺乏有效的预防和治疗策略。
我们的研究旨在评估在紫杉醇诱导的神经病变大鼠模型中早期口服含植物大麻素四氢大麻酚(THC)和大麻二酚(CBD)的药用级制剂的影响。
实验设计为将紫杉醇和不同THC与CBD比例(THC:CBD 1:1和THC:CBD 1:20)的大麻素制剂共同给予成年雄性大鼠。评估机械和热敏感性、运动活动、垂直探索行为、焦虑相关参数、体重增加、食物和水消耗以及肝功能。
每日给予THC:CBD 1:1成功预防了紫杉醇诱导的冷痛觉过敏,而THC:CBD 1:20有效预防了热和机械超敏反应。此外,THC:CBD 1:1制剂恢复了被紫杉醇显著降低的竖毛行为。相反,两种大麻素制剂均无法抵消紫杉醇诱导的运动减少、垂直探索活动减少、焦虑样行为增加、体重增加减弱或食物和水摄入量减少。然而,所使用的制剂在接受紫杉醇的动物中未引起进一步改变或毒性,且未检测到肝损伤迹象。
我们的结果表明两种THC:CBD制剂对疼痛相关行为和自发活动有不同的治疗效果,特别是在外周神经病变的背景下。这些制剂不仅是管理疼痛的有前景的治疗策略,而且对于增强癌症患者的日常活动和改善生活质量也是如此。