首页> 美国卫生研究院文献>Journal of Neural Transplantation >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
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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

机译:在大鼠疼痛记忆模型中cAMP / PKA / CREB途径的抑制作用有助于扣带前皮层中电针的镇痛作用

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摘要

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.
机译:疼痛记忆被认为是顽固性慢性疼痛的内在因素。我们先前的研究表明,电针(EA)可以减轻疼痛记忆的恢复。本研究旨在观察EA和消炎痛(一种非甾体类抗炎药,NSAIDs)在大鼠疼痛记忆模型中的不同作用。为了探索蛋白激酶A(PKA)在疼痛记忆中的关键作用,将PKA抑制剂微注射入模型大鼠的前扣带回皮质(ACC)中。我们进一步研究了环状磷酸腺苷(cAMP),PKA,cAMP反应元件结合蛋白(CREB)和cAMP / PKA / CREB途径在疼痛记忆中的作用,以探讨潜在的分子机制。结果表明,当消炎痛失败时,EA减轻了疼痛记忆的恢复。 AKA内注射PKA抑制剂可阻止疼痛记忆的发生。 EA降低了疼痛记忆模型大鼠ACC中cAMP,PKA和CREB的活化以及cAMP / PKA和PKA / CREB的共表达水平,但消炎痛失败了。目前的发现确定了PKA在ACC中恢复疼痛记忆中的关键作用。我们提出EA对疼痛记忆的正确机制可能是由于EA对cAMP / PKA / CREB信号通路的部分抑制。

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