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瑞芬太尼预处理通过激活背侧迷走神经复合体中的神经元减轻大鼠肝缺血再灌注损伤。

Remifentanil Preconditioning Attenuates Hepatic Ischemia-Reperfusion Injury in Rats via Neuronal Activation in Dorsal Vagal Complex.

机构信息

Department of Anesthesiology, Eastern Hepatobiliary Surgery Hospital, the Second Military Medical University, Shanghai, China.

Department of Anesthesiology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Mediators Inflamm. 2018 May 10;2018:3260256. doi: 10.1155/2018/3260256. eCollection 2018.

Abstract

Remifentanil, an ultra-short acting opiate, has been reported to protect against hepatic ischemia-reperfusion injury, which is a major cause of postoperative liver dysfunction. The objective of this study was to determine whether a central vagal pathway is involved in this protective procedure. Rat models of hepatic ischemia-reperfusion were used in the experimental procedures. The results revealed that intravenous pretreatment with remifentanil decreased serum aminotransferases and hepatic histologic damage; however, an intraperitoneal injection of -opioid receptor antagonist did not abolish the protection of remifentanil preconditioning. c-Fos immunofluorescence of the brain stem showed that dorsal motor nucleus of the vagus was activated after remifentanil preconditioning. Moreover, serum alanine aminotransferase, histopathologic damage, and apoptosis decreased in remifentanil preconditioning group compared to vagotomized animals with remifentanil preconditioning, and there was no statistical difference of TNF- and IL-6 between NS/Va and RPC/Va groups. In addition, remifentanil microinjection into dorsal vagal complex decreased serum aminotransferases, inflammatory cytokines, and hepatic histologic injury and apoptosis, and these effects were also abolished by a peripheral hepatic vagotomy. In conclusion, remifentanil preconditioning conferred liver protection against ischemia-reperfusion injury, which was mediated by the central vagal pathway.

摘要

瑞芬太尼是一种超短效阿片类药物,已被报道可预防肝缺血再灌注损伤,这是术后肝功能障碍的主要原因。本研究的目的是确定中枢迷走神经通路是否参与这种保护过程。在实验过程中使用了肝缺血再灌注的大鼠模型。结果表明,瑞芬太尼静脉预处理可降低血清转氨酶和肝组织损伤;然而,腹腔内注射 - 阿片受体拮抗剂并未消除瑞芬太尼预处理的保护作用。脑干的 c-Fos 免疫荧光显示,瑞芬太尼预处理后迷走神经背核被激活。此外,与迷走神经切断的瑞芬太尼预处理动物相比,瑞芬太尼预处理组的血清丙氨酸转氨酶、组织病理学损伤和细胞凋亡减少,且 NS/Va 和 RPC/Va 组之间 TNF-α 和 IL-6 无统计学差异。此外,瑞芬太尼微量注射到迷走神经背核复合体可降低血清转氨酶、炎症细胞因子、肝组织学损伤和细胞凋亡,而外周肝迷走神经切断术也消除了这些作用。总之,瑞芬太尼预处理可防止肝缺血再灌注损伤,这是通过中枢迷走神经通路介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2f0/5976991/7c67b2122e58/MI2018-3260256.004.jpg

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