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抑制环磷酸腺苷/蛋白激酶A/环磷腺苷反应元件结合蛋白信号通路有助于电针在大鼠疼痛记忆模型中对前扣带回皮质产生镇痛作用。

Inhibition of the cAMP/PKA/CREB Pathway Contributes to the Analgesic Effects of Electroacupuncture in the Anterior Cingulate Cortex in a Rat Pain Memory Model.

作者信息

Shao Xiao-Mei, Sun Jing, Jiang Yong-Liang, Liu Bo-Yi, Shen Zui, Fang Fang, Du Jun-Ying, Wu Yuan-Yuan, Wang Jia-Ling, Fang Jian-Qiao

机构信息

Department of Neurobiology and Acupuncture Research, The Third Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, China.

Department of Acupuncture and Moxibustion, Wenzhou Hospital Affiliated to Zhejiang University of Traditional Chinese Medicine, Wenzhou, China.

出版信息

Neural Plast. 2016;2016:5320641. doi: 10.1155/2016/5320641. Epub 2016 Dec 20.

Abstract

Pain memory is considered as endopathic factor underlying stubborn chronic pain. Our previous study demonstrated that electroacupuncture (EA) can alleviate retrieval of pain memory. This study was designed to observe the different effects between EA and indomethacin (a kind of nonsteroid anti-inflammatory drugs, NSAIDs) in a rat pain memory model. To explore the critical role of protein kinase A (PKA) in pain memory, a PKA inhibitor was microinjected into anterior cingulate cortex (ACC) in model rats. We further investigated the roles of the cyclic adenosine monophosphate (cAMP), PKA, cAMP response element-binding protein (CREB), and cAMP/PKA/CREB pathway in pain memory to explore the potential molecular mechanism. The results showed that EA alleviates the retrieval of pain memory while indomethacin failed. Intra-ACC microinjection of a PKA inhibitor blocked the occurrence of pain memory. EA reduced the activation of cAMP, PKA, and CREB and the coexpression levels of cAMP/PKA and PKA/CREB in the ACC of pain memory model rats, but indomethacin failed. The present findings identified a critical role of PKA in ACC in retrieval of pain memory. We propose that the proper mechanism of EA on pain memory is possibly due to the partial inhibition of cAMP/PKA/CREB signaling pathway by EA.

摘要

疼痛记忆被认为是顽固性慢性疼痛的内在致病因素。我们之前的研究表明,电针(EA)可以减轻疼痛记忆的提取。本研究旨在观察EA与吲哚美辛(一种非甾体抗炎药,NSAIDs)在大鼠疼痛记忆模型中的不同作用。为了探究蛋白激酶A(PKA)在疼痛记忆中的关键作用,将PKA抑制剂微量注射到模型大鼠的前扣带回皮质(ACC)中。我们进一步研究了环磷酸腺苷(cAMP)、PKA、cAMP反应元件结合蛋白(CREB)以及cAMP/PKA/CREB信号通路在疼痛记忆中的作用,以探索潜在的分子机制。结果表明,EA可减轻疼痛记忆的提取,而吲哚美辛则无效。在ACC内微量注射PKA抑制剂可阻断疼痛记忆的发生。EA降低了疼痛记忆模型大鼠ACC中cAMP、PKA和CREB的激活以及cAMP/PKA和PKA/CREB的共表达水平,但吲哚美辛则无效。本研究结果确定了PKA在ACC中对疼痛记忆提取的关键作用。我们提出,EA对疼痛记忆的适当作用机制可能是由于EA对cAMP/PKA/CREB信号通路的部分抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b91/5206448/6bbf4fb352c8/NP2016-5320641.001.jpg

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