Olga Feigni Youyi Marcelle, Marius Mbiantcha, William Yousseu Nana, Gonzal Tsafack Eric, Flore Djuichou Nguemnang Stephanie, Chrétien Noungoua Mbeugangkeng, Gisèle Atsafack Mboudem Lylie, Gilbert Ateufack
Laboratory of Animal Physiology and Phytopharmacology, Department of Animal Biology, Faculty of Science, University of Dschang, Dschang, Cameroon.
Laboratory of Biology and Physiology of Animal Organisms, Department of Biology of Animal Organisms, Faculty of Science, The University of Douala Cameroon, P.O. Box 24157, Douala, Cameroon.
Adv Pharmacol Pharm Sci. 2024 Dec 12;2024:8822369. doi: 10.1155/adpp/8822369. eCollection 2024.
Linn. (, Vitaceae) is a plant reported to treat injured tendons, broken bones, asthma, stomach ache, scurvy, and digestive disorders. The present study evaluated the antihyperalgesic effects of ethanolic extract of Linn. Vincristine sulfate (100 μg/kg, i.p.) was administered in rats for 10 days with 2 days break to induce painful peripheral neuropathy. Mechanical hyperalgesia and allodynia tests were performed to assess the threshold of painful neuropathy. Calcium levels in the sciatic nerve, oxidant stress markers, and levels of GABA and 5-HT were also determined in the brain and spinal cord after 15 days. Ethanolic extract of (180 and 360 mg/kg) and pregabalin (50 mg/kg) were administered for 15 consecutive days. The results revealed that the extract significantly ( < 0.001) inhibited hyperalgesia and allodynia in animals after vincristine administration. The extract decreased total calcium levels in the sciatic nerve, MDA levels while increasing GSH activity, 5-HT level, as well as GABA levels in the brain and spinal cord. The results of this study suggest that the ethanolic extract of uses antioxidant capacity, calcium inhibitory action, and neuromodulation of GABA and 5-HT to prevent the development of painful neuropathy after vincristine administration. This demonstrates that is a promising molecule for the management of peripheral neuropathic pain induced by anticancer drugs.
林奈(葡萄科)是一种据报道可治疗肌腱损伤、骨折、哮喘、胃痛、坏血病和消化系统疾病的植物。本研究评估了[植物名称未完整给出]乙醇提取物的抗痛觉过敏作用。硫酸长春新碱(100μg/kg,腹腔注射)在大鼠中给药10天,间隔2天,以诱导疼痛性周围神经病变。进行机械性痛觉过敏和异常性疼痛测试以评估疼痛性神经病变的阈值。在15天后还测定了坐骨神经中的钙水平、氧化应激标志物以及大脑和脊髓中γ-氨基丁酸(GABA)和5-羟色胺(5-HT)的水平。[植物名称未完整给出]乙醇提取物(180和360mg/kg)和普瑞巴林(50mg/kg)连续给药15天。结果显示,提取物在长春新碱给药后显著(P<0.001)抑制了动物的痛觉过敏和异常性疼痛。提取物降低了坐骨神经中的总钙水平、丙二醛(MDA)水平,同时增加了谷胱甘肽(GSH)活性、5-HT水平以及大脑和脊髓中的GABA水平。本研究结果表明,[植物名称未完整给出]乙醇提取物利用抗氧化能力、钙抑制作用以及对GABA和5-HT的神经调节作用来预防长春新碱给药后疼痛性神经病变的发展。这表明[植物名称未完整给出]是一种用于管理抗癌药物诱导的周围神经性疼痛的有前景的分子。