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[急性疼痛向慢性疼痛转化过程中外周蛋白激酶Cε通路的研究进展及电针干预的应用可能性]

[Advances of researches on peripheral PKCε pathway during transformation from acute to chronic pain and possibility of application of electroacupuncture intervention].

作者信息

Sun Hai-Ju, Wang Si-Si, Li Xiao-Yu, Du Jun-Ying, Fang Jian-Qiao, Fang Jun-Fan

机构信息

The Third Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou 310053, China.

Zhejiang Chinese Medical University, Hangzhou 310053, China.

出版信息

Zhen Ci Yan Jiu. 2019 Jul 25;44(7):543-7. doi: 10.13702/j.1000-0607.180542.

DOI:10.13702/j.1000-0607.180542
PMID:31368289
Abstract

Protein kinase Cε (PKCε) is a transforming oncogene and plays an important role in many cellular processing. In the present paper, we review the development of experimental researches on the acute-chronic pain transformation. Results indicated that prostaglandin E2 (PGE2) / EP1 receptor-Gq-PKCε is an important signaling pathway to modulate chronic pain in peripheral dorsal root ganglion (DRG) neurons, and also plays a role in the later stage of hyperalgesia during transformation from acute to chronic pain. PKCε in DRG neurons induces mechanical and thermal hypersensitivity respectively by over expression of transient receptor potential vanilloid 1 (TRPV1) and TRP ankyrin-1 (TRPA1), further mediating the transformation from acute to chronic pain. Whereas, PGE2-evoked activation of EP1-Gq-PKCε signaling may be the key link in initiating the pain translation process through regulating downstream TRPA1 and TRPV1. Electroacupuncture (EA) has been used to effectively relieving various types of acute and chronic pain for decades, and can significantly inhibit the expression of PKCε and its upstream and downstream molecules. Therefore, it can be inferred that there exists a possibility of EA interventions in interfering the transformation from acute to chronic pain by regulating peripheral PKCε signaling pathway.

摘要

蛋白激酶Cε(PKCε)是一种转化癌基因,在许多细胞过程中发挥重要作用。在本文中,我们综述了急慢性疼痛转化的实验研究进展。结果表明,前列腺素E2(PGE2)/EP1受体-Gq-PKCε是调节外周背根神经节(DRG)神经元慢性疼痛的重要信号通路,在急性疼痛向慢性疼痛转化过程中的痛觉过敏后期也发挥作用。DRG神经元中的PKCε分别通过瞬时受体电位香草酸亚型1(TRPV1)和锚蛋白1型瞬时受体电位通道(TRPA1)的过表达诱导机械性和热超敏反应,进一步介导急性疼痛向慢性疼痛的转化。而PGE2诱发的EP1-Gq-PKCε信号激活可能是通过调节下游TRPA1和TRPV1启动疼痛转化过程的关键环节。几十年来,电针(EA)已被用于有效缓解各种急慢性疼痛,并且可以显著抑制PKCε及其上下游分子的表达。因此,可以推断电针有可能通过调节外周PKCε信号通路干预急性疼痛向慢性疼痛的转化。

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