首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Rostral ventromedial medulla‐mediated descending facilitation following P2X7 receptor activation is involved in the development of chronic post‐operative pain
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Rostral ventromedial medulla‐mediated descending facilitation following P2X7 receptor activation is involved in the development of chronic post‐operative pain

机译:rostral enveromedial medulla介导的p2x7受体活化后的下降促进促进促进促进慢性术后疼痛的发育

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Abstract Chronic postsurgical pain ( CPSP ) remains a medical problem. Whether the descending modulation of nociceptive transmission from the rostral ventromedial medulla ( RVM ) plays a role in CPSP induced by skin/muscle incision and retraction ( SMIR ) in the thigh is still unknown. In this study, we found that SMIR surgery, which induced either bilateral or unilateral mechanical allodynia, activated microglia, and up‐regulated?interleukin‐1β ( IL ‐1β), an important cytokine, and 8‐hydroxyguanine, an oxidative stress marker in the RVM . In addition, the release of 5‐hydroxytryptamine (5‐ HT ) was increased in the ipsilateral and contralateral RVM in rats with either bilateral or unilateral pain following SMIR . The 5‐ HT level increase, 5‐ HT 3 receptor (5‐ HT 3R) up‐regulation, and microglia activation were found bilaterally in SMIR rats with bilateral pain, but only ipsilaterally in SMIR rats with unilateral pain. The intrathecal injection of the 5‐ HT 3R antagonist Y25130 prevented the development of CPSP and the activation of spinal microglia induced by SMIR . Furthermore, P2X7 receptor (P2X7R) was up‐regulated in microglia in the RVM . The microinjection of the P2X7R antagonist brilliant blue G ( BBG , a non‐competitive P2X7R antagonist) into the RVM prevented the development of mechanical allodynia, inhibited the activation of microglia, and decreased the expression of IL ‐1β and 8‐hydroxyguanine in the RVM following SMIR . Importantly, BBG injected into the RVM also decreased the activation of microglia and the level of 5‐ HT in the lumbar 3 (L3) spinal cord. The microinjection of the P2X7R agonist Bz ATP , the NADPH oxidase activator phorbol‐12‐myristate‐13‐acetate, or IL ‐1β into the RVM induced bilateral mechanical allodynia, microglia activation, and 5‐ HT release in the L3 spinal dorsal horn. Taken together, P2X7R activation in microglia in the RVM following SMIR might be responsible for the development of CPSP via activating descending serotonergic pathway. Open science badges This article has received a badge for *Open Materials* because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at? https://cos.io/our-services/open-science-badges/ .
机译:摘要慢性术后疼痛(CPSP)仍然是一个医学问题。是否从延髓腹内侧髓质(RVM)痛觉传递的下降调制在大腿起着CPSP作用通过皮肤/肌肉切口和缩回(SMIR)诱导的仍然是未知的。在这项研究中,我们发现,SMIR手术,从而诱发或者双侧或单侧机械异常性疼痛,活化小胶质细胞,和上调?白介素1β(IL-1β),一个重要的细胞因子,和8-羟基鸟嘌呤,在氧化应激标记在RVM。此外,5-羟色胺(5-HT)的释放是在同侧和对侧RVM与以下任一SMIR双侧或单侧疼痛增加的影响。该5-HT水平升高,5-HT 3受体(5-HT 3R)上调和小胶质细胞活化是在SMIR大鼠双侧疼痛双边发现,但仅在同侧大鼠SMIR单侧疼痛。 5-羟色胺拮抗剂3R Y25130的鞘内注射防止CPSP的发展和由SMIR引起的大鼠脊髓小胶质细胞的活化。在小神经胶质细胞RVM此外,P2X7受体(P2X7R)上调。的P2X7R的拮抗剂显微注射亮蓝G(BBG,非竞争性拮抗剂P2X7R)插入防止机械异常性疼痛的发展RVM,抑制小胶质细胞的激活,和在RVM降低IL-1β的表达和8-羟基以下SMIR。重要的是,BBG注入RVM也降低小胶质细胞活化和5-羟色胺的腰3(L3)脊髓水平。的P2X7R激动剂的Bz ATP,NADPH氧化酶激活剂佛波醇-12-肉豆蔻酸酯-13-乙酸酯,或IL-1β的显微注射入RVM诱导的两侧的机械异常性疼痛,小胶质细胞活化,而在L3脊髓背角的5-HT的释放。总之,P2X7R激活以下SMIR在RVM小胶质细胞可能是负责通过激活降血清素途径CPSP的发展。开放式科学徽章本文已收到*开放材料的徽章*,因为它提供了所有相关信息以在手稿中重现研究。本文的完整开放科学披露表格可以在文章的末尾找到。关于开放实践徽章的更多信息,可以发现? https://cos.io/our-services/open-science-badges/。

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