From the Department of Anesthesiology, Southwest Hospital, Third Military Medical University, Chongqing, China.
Anaesthetics, Pain Medicine and Intensive Care, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, Chelsea and Westminster Campus, London, United Kingdom.
Anesth Analg. 2020 Apr;130(4):1054-1062. doi: 10.1213/ANE.0000000000003820.
Organ ischemia-reperfusion injury often induces local and systemic inflammatory responses, which in turn worsen organ injury. These inflammatory responses can be regulated by the central nervous system, particularly by the vagal nerve and nicotinic acetylcholine receptors, which are the key components of cholinergic anti-inflammatory pathway. Activation of the cholinergic anti-inflammatory pathway can suppress excessive inflammatory responses and be a potential strategy for prevention of ischemia-reperfusion injury of organs including the kidney.
Vagal nerve activity, plasma acetylcholine, catecholamine and inflammatory mediators, renal tissue injury, and cell death were measured in mice with bilateral renal ischemia/reperfusion with or without treatment with dexmedetomidine (Dex), an α2-adrenergic receptor agonist.
Dex significantly increased the discharge frequency of the cervical vagal nerve by up to 142 Hz (mean) (P < .001), and preserved kidney gross morphology and structure and attenuated cell apoptosis after ischemia-reperfusion. Furthermore, Dex also significantly increased acetylcholine release to 135.8 pmol/L (median) when compared to that (84.7 pmol/L) in the sham group (P < .001) and reduced the levels of several inflammatory mediators induced by renal ischemia/reperfusion. All the effects were abolished by vagotomy, splenectomy, or combinative administration of atipamezole, an α2-adrenergic receptor antagonist.
Our findings suggest that Dex provides renoprotection, at least in part, through anti-inflammatory effects of the parasympathetic nervous system activation in addition to its direct actions on α2-adrenergic receptors.
器官缺血再灌注损伤常引起局部和全身炎症反应,进而加重器官损伤。这些炎症反应可以被中枢神经系统调节,特别是通过迷走神经和烟碱型乙酰胆碱受体,它们是胆碱能抗炎途径的关键组成部分。激活胆碱能抗炎途径可以抑制过度的炎症反应,是预防包括肾脏在内的器官缺血再灌注损伤的潜在策略。
在双侧肾缺血再灌注的小鼠中,测量迷走神经活动、血浆乙酰胆碱、儿茶酚胺和炎症介质、肾组织损伤和细胞死亡,并用右美托咪定(Dex)治疗,Dex 是一种α2-肾上腺素能受体激动剂。
Dex 可使颈迷走神经放电频率平均增加 142 Hz(P <.001),并保留肾大体形态和结构,减轻缺血再灌注后的细胞凋亡。此外,与假手术组(84.7 pmol/L)相比,Dex 还显著增加了乙酰胆碱的释放,达到 135.8 pmol/L(中位数)(P <.001),并降低了肾缺血再灌注诱导的几种炎症介质的水平。所有这些作用均被迷走神经切断术、脾切除术或α2-肾上腺素能受体拮抗剂阿替美唑联合给药所消除。
我们的研究结果表明,Dex 通过激活副交感神经系统的抗炎作用以及其对α2-肾上腺素能受体的直接作用,提供肾脏保护作用,至少部分如此。