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首页> 外文期刊>Molecular pain >Intraoperative electroacupuncture relieves remifentanil-induced postoperative hyperalgesia via inhibiting spinal glial activation in rats
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Intraoperative electroacupuncture relieves remifentanil-induced postoperative hyperalgesia via inhibiting spinal glial activation in rats

机译:术中电针通过抑制大鼠脊髓神经胶质细胞的活化来缓解瑞芬太尼引起的术后痛觉过敏

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Accumulating studies have suggested that remifentanil, the widely-used opioid analgesic in clinical anesthesia, can activate the pronociceptive systems and enhance postoperative pain. Glial cells are thought to be implicated in remifentanil-induced hyperalgesia. Electroacupuncture is a complementary therapy to relieve various pain conditions with few side effects, and glial cells may be involved in its antinociceptive effect. In this study, we investigated whether intraoperative electroacupuncture could relieve remifentanil-induced postoperative hyperalgesia by inhibiting the activation of spinal glial cells, the production of spinal proinflammatory cytokines, and the activation of spinal mitogen-activated protein kinases. A rat model of remifentanil-induced postoperative hyperalgesia was used in this study. Electroacupuncture during surgery was conducted at bilateral Zusanli (ST36) acupoints. Behavior tests, including mechanical allodynia and thermal hyperalgesia, were performed at different time points. Astrocytic marker glial fibrillary acidic protein, microglial marker Iba1, proinflammatory cytokines, and phosphorylated mitogen-activated protein kinases in the spinal cord were detected by Western blot and/or immunofluorescence. Mechanical allodynia and thermal hyperalgesia were induced by both surgical incision and remifentanil infusion, and remifentanil infusion significantly exaggerated and prolonged incision-induced pronociceptive effects. Glial fibrillary acidic protein, Iba1, proinflammatory cytokines (interleukin-1β and tumor necrosis factor-α), and phosphorylated mitogen-activated protein kinases (p-p38, p-JNK, and p-ERK1/2) were upregulated after surgical incision, remifentanil infusion, and especially after their combination. Intraoperative electroacupuncture significantly attenuated incision- and/or remifentanil-induced pronociceptive effects, spinal glial activation, proinflammatory cytokine upregulation, and phosphorylated mitogen-activated protein kinase upregulation. Our study suggests that remifentanil-induced postoperative hyperalgesia can be relieved by intraoperative electroacupuncture via inhibiting the activation of spinal glial cells, the upregulation of spinal proinflammatory cytokines, and the activation of spinal mitogen-activated protein kinases.
机译:越来越多的研究表明,瑞芬太尼是临床麻醉中广泛使用的阿片类镇痛药,可以激活触觉感受系统并增加术后疼痛。胶质细胞被认为与瑞芬太尼诱导的痛觉过敏有关。电针是一种缓解各种疼痛状况且几乎没有副作用的辅助疗法,神经胶质细胞可能参与了其抗伤害感受作用。在这项研究中,我们研究了术中电针能否通过抑制脊髓神经胶质细胞的激活,脊髓促炎性细胞因子的产生以及脊髓促分裂原激活的蛋白激酶的激活来缓解瑞芬太尼引起的术后痛觉过敏。在这项研究中使用了瑞芬太尼诱导的术后痛觉过敏的大鼠模型。手术期间在双足足三里(ST36)穴位进行电针刺。在不同的时间点进行行为测试,包括机械性异常性疼痛和热痛觉过敏。 Western印迹和/或免疫荧光检测脊髓中星形胶质细胞标记神经胶质纤维酸性蛋白,小胶质细胞标记Iba1,促炎细胞因子和磷酸化的丝裂原活化蛋白激酶。机械性异常性疼痛和热痛觉过敏由手术切口和瑞芬太尼输注引起,而瑞芬太尼输注显着夸大并延长了切口诱发的伤害感受。手术切口后,胶质纤维酸性蛋白,Iba1,促炎细胞因子(白介素-1β和肿瘤坏死因子-α)以及磷酸化的丝裂原活化蛋白激酶(p-p38,p-JNK和p-ERK1 / 2)被上调,瑞芬太尼输注,尤其是两者合用后。术中电针显着减弱切口和/或瑞芬太尼诱导的伤害感受作用,脊髓神经胶质活化,促炎性细胞因子上调以及磷酸化有丝分裂原激活的蛋白激酶上调。我们的研究表明,术中电针可通过抑制脊髓神经胶质细胞的激活,脊髓促炎性细胞因子的上调以及脊髓促分裂原激活的蛋白激酶的激活来缓解瑞芬太尼引起的术后痛觉过敏。

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