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闹羊花毒素VI间接靶向Cav2.2通道-乙基马来酰亚胺敏感融合蛋白以减轻神经性疼痛。

Rhodojaponin VI indirectly targets Cav2.2 channels -ethylmaleimide-sensitive fusion protein to alleviate neuropathic pain.

作者信息

Chen Keliang, Wang Tao, Li Yong, Wu Jun, Zhao Cheng-Xiao, Liu Sheng, Sun Fengrun, Fang Yehong, Hu Jiahuan, Hu Jinping, Zhang Chong-Jing, Yu Haibo, Ma Chao, Yu Shi-Shan

机构信息

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.

Institute of Basic Medical Sciences, Neuroscience Center, Chinese Academy of Medical Sciences, Department of Human Anatomy, Histology and Embryology, School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.

出版信息

Acta Pharm Sin B. 2023 Mar;13(3):1326-1336. doi: 10.1016/j.apsb.2023.01.021. Epub 2023 Feb 3.

Abstract

Neuropathic pain is a chronic disease that severely afflicts the life and emotional status of patients, but currently available treatments are often ineffective. Novel therapeutic targets for the alleviation of neuropathic pain are urgently needed. Rhodojaponin VI, a grayanotoxin from , showed remarkable antinociceptive efficacy in models of neuropathic pain, but its biotargets and mechanisms are unknown. Given the reversible action of rhodojaponin VI and the narrow range over which its structure can be modified, we perforwmed thermal proteome profiling of the rat dorsal root ganglion to determine the protein target of rhodojaponin VI. -Ethylmaleimide-sensitive fusion (NSF) was confirmed as the key target of rhodojaponin VI through biological and biophysical experiments. Functional validation showed for the first time that NSF facilitated trafficking of the Cav2.2 channel to induce an increase in Ca current intensity, whereas rhodojaponin VI reversed the effects of NSF. In conclusion, rhodojaponin VI represents a unique class of analgesic natural products targeting Cav2.2 channels NSF.

摘要

神经性疼痛是一种严重影响患者生活和情绪状态的慢性疾病,但目前可用的治疗方法往往无效。迫切需要用于缓解神经性疼痛的新型治疗靶点。闹羊花毒素VI是一种从[来源未明确]提取的灰毒素,在神经性疼痛模型中显示出显著的镇痛效果,但其生物靶点和作用机制尚不清楚。鉴于闹羊花毒素VI的可逆作用及其结构可修饰范围狭窄,我们对大鼠背根神经节进行了热蛋白质组分析,以确定闹羊花毒素VI的蛋白质靶点。通过生物学和生物物理实验证实,N - 乙基马来酰亚胺敏感因子(NSF)是闹羊花毒素VI的关键靶点。功能验证首次表明,NSF促进Cav2.2通道的转运,从而导致钙电流强度增加,而闹羊花毒素VI可逆转NSF的作用。总之,闹羊花毒素VI代表了一类独特的靶向Cav2.2通道 - NSF的镇痛天然产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8f/10031280/e21058650ee1/ga1.jpg

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