乌头生物碱镇痛作用及机制研究进展

被引:57
作者
黄茜
孙明丽
李腾飞
王永祥
机构
[1] 上海交通大学药学院King’sLab
关键词
乌头碱; 草乌甲素; 雪上一枝蒿甲素; 高乌甲素; 镇痛; 强啡肽; 小胶质细胞;
D O I
暂无
中图分类号
R285 [中药药理学];
学科分类号
100806 [中药药理学];
摘要
乌头属植物资源丰富、药用历史悠久、在临床上应用广泛。二萜生物碱是乌头属植物的主要药理活性成分,按结构可分为C-18型、C-19型、C-20型和双二萜生物碱,具有抗炎、镇痛、抗肿瘤等活性。本文旨在综述临床中广泛使用的乌头属药物中几种主要二萜生物碱,包括草乌甲素(C-19型)、雪上一枝蒿甲素(C-20型)、高乌甲素(C-18型)及乌头碱(C-19型)的镇痛作用和机制的研究进展,以及乌头炮制的药理学依据。草乌甲素、雪上一枝蒿甲素、高乌甲素和乌头碱在多种疼痛模型和临床研究中均表现出良好的镇痛作用,其镇痛作用系通过Gs/c AMP/PKA/p38β/CREB信号通路,刺激脊髓背角的小胶质细胞释放强啡肽,随后作用于神经突触后膜神经元上的κ-阿片受体而产生。乌头碱经炮制生成苯甲酰乌头原碱,毒性降低,治疗指数增加。此外,多种乌头属二萜生物碱和乌头提取物均不产生镇痛耐受作用,并能有效抑制吗啡的镇痛耐受,亦与它们的镇痛作用机制有关。
引用
收藏
页码:21 / 32
页数:12
相关论文
共 60 条
[1]
Cynandione A attenuates neuropathic pain through p38β MAPK-mediated spinal microglial expression of β-endorphin[J] Qian Huang;Xiao-Fang Mao;Hai-Yun Wu;Hao Liu;Ming-Li Sun;Xiao Wang;Yong-Xiang Wang Brain Behavior and Immunity 2017,
[2]
Morroniside, a secoiridoid glycoside from Cornus officinalis, attenuates neuropathic pain by activation of spinal glucagon-like peptide-1 receptors [J].
Xu, Meng ;
Wu, Hai-Yun ;
Liu, Hao ;
Gong, Nian ;
Wang, Yi-Rui ;
Wang, Yong-Xiang .
BRITISH JOURNAL OF PHARMACOLOGY, 2017, 174 (07) :580-590
[3]
Shanzhiside methylester; the principle effective iridoid glycoside from the analgesic herb Lamiophlomis rotata ; reduces neuropathic pain by stimulating spinal microglial β-endorphin expression[J] Hui Fan;Teng-Fei Li;Nian Gong;Yong-Xiang Wang Neuropharmacology 2016,
[4]
Aconitum -derived bulleyaconitine A exhibits anti-hypersensitivity through direct stimulating dynorphin A expression in spinal microglia[J] Teng-Fei Li;Hui Fan;Yong-Xiang Wang Journal of Pain 2015,
[5]
Peptidic exenatide and herbal catalpol mediate neuroprotection via the hippocampal GLP-1 receptor/β-endorphin pathway[J] Yu Jia;Nian Gong;Teng-Fei Li;Bin Zhu;Yong-Xiang Wang Pharmacological Research 2015,
[6]
Development and validation of an LC-MS/MS method for the determination of bullatine A in rat plasma: application to a pharmacokinetic study [J].
Teng, Shi-Yong ;
Zhang, Si-Xi ;
Niu, Kai ;
Zhai, Li-Jie ;
Wang, Shi-Ji .
BIOMEDICAL CHROMATOGRAPHY, 2015, 29 (12) :1798-1804
[7]
Bulleyaconitine A depresses neuropathic pain and potentiation at C-fiber synapses in spinal dorsal horn induced by paclitaxel in rats[J] He-Quan Zhu;Jing Xu;Kai-Feng Shen;Rui-Ping Pang;Xu-Hong Wei;Xian-Guo Liu Experimental Neurology 2015,
[8]
In Vivo and In Vitro Metabolites from the Main Diester and Monoester Diterpenoid Alkaloids in a Traditional Chinese Herb; the Aconitum Species[J] Min Zhang;Chong-sheng Peng;Xiao-bo Li;Roja Rahimi Evidence-Based Complementary and Alternative Medicine 2015,
[9]
The non-peptide GLP-1 receptor agonist WB4-24 blocks inflammatory nociception by stimulating β-endorphin release from spinal microglia [J].
Fan, Hui ;
Gong, Nian ;
Li, Teng-Fei ;
Ma, Ai-Niu ;
Wu, Xiao-Yan ;
Wang, Ming-Wei ;
Wang, Yong-Xiang .
BRITISH JOURNAL OF PHARMACOLOGY, 2015, 172 (01) :64-79
[10]
Geniposide and its iridoid analogs exhibit antinociception by acting at the spinal GLP-1 receptors[J] Nian Gong;Hui Fan;Ai-Niu Ma;Qi Xiao;Yong-Xiang Wang Neuropharmacology 2014,