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有效植物成分乌头碱:治疗三叉神经痛的现实方法。

An Effective Phytoconstituent Aconitine: A Realistic Approach for the Treatment of Trigeminal Neuralgia.

机构信息

Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Gazi University, 06490 Ankara, Turkey.

Department of Pharmacognosy, Faculty of Pharmacy, Gazi University, 06330 Ankara, Turkey.

出版信息

Mediators Inflamm. 2021 Apr 14;2021:6676063. doi: 10.1155/2021/6676063. eCollection 2021.

Abstract

Trigeminal neuralgia pain remains a challenge to treat. Natural compounds may be promising options for relieving pain. This study was aimed at investigating the effects of aconitine in a rat model of trigeminal neuralgia pain. Infraorbital nerve chronic constriction injury was performed in adult Wistar Albino rats. After the neuropathic pain developed, the rats were assigned to one of the treatment groups: carbamazepine 40 or 80 mg/kg; aconitine 0.25, 0.50, or 0.75 mg/kg; or saline injection (control group). Behavioral testing with von Frey filaments and the rotarod test were carried out before the surgical procedure and on the 24th to 29th postoperative days. Following the completion of tests, ipsilateral and contralateral spinal cords were harvested for Western blot analyses to assess NR-1 protein expression. ANOVA followed by Mann-Whitney test was performed for the statistical analyses. values of <0.05 were considered significant. Aconitine significantly reduced mechanical sensitivity in a dose-dependent manner. A significant reduction in motor coordination was noted for the higher doses of aconitine which was similar with the 40 and 80 mg/kg doses of carbamazepine. NR-1 expression was reduced in the ipsilateral spinal cord, whereas no significant difference was noted between the groups in the expression of NR-1 in the contralateral spinal cord. Aconitine had a significant pain relieving effect, which was similar to carbamazepine, in a dose-dependent manner. Aconitine may be an alternative pharmacological agent for the control of trigeminal neuralgia pain.

摘要

三叉神经痛的治疗仍然具有挑战性。天然化合物可能是缓解疼痛的有前途的选择。本研究旨在研究乌头碱在三叉神经痛大鼠模型中的作用。在成年 Wistar 白化大鼠中进行眶下神经慢性缩窄损伤。在神经性疼痛发展后,将大鼠分为以下治疗组之一:卡马西平 40 或 80mg/kg;乌头碱 0.25、0.50 或 0.75mg/kg;或生理盐水注射(对照组)。在手术前和术后第 24 至 29 天进行 von Frey 纤维和旋转棒试验进行行为测试。完成测试后,收获同侧和对侧脊髓进行 Western blot 分析,以评估 NR-1 蛋白表达。采用 ANOVA followed by Mann-Whitney 检验进行统计分析。<0.05 被认为具有统计学意义。乌头碱以剂量依赖性方式显著降低机械敏感性。乌头碱较高剂量时观察到运动协调能力显著降低,与卡马西平 40 和 80mg/kg 剂量相似。同侧脊髓中 NR-1 表达减少,而对侧脊髓中 NR-1 表达在各组之间无显著差异。乌头碱具有显著的镇痛作用,与卡马西平相似,呈剂量依赖性。乌头碱可能是控制三叉神经痛的替代药理学药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9b5/8062177/25867f78e462/MI2021-6676063.001.jpg

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