Neumann Silke, Shields Nicholas J, Balle Thomas, Chebib Mary, Clarkson Andrew N
Department of Pathology, University of Otago, Dunedin 9054, New Zealand.
Department of Anatomy, Brain Health Research Centre and Brain Research New Zealand, University of Otago, P.O. Box 913, Dunedin 9054, New Zealand.
Int J Mol Sci. 2015 Dec 4;16(12):29029-46. doi: 10.3390/ijms161226141.
Stroke is one of the leading causes of death and long-term disability, with limited treatment options available. Inflammation contributes to damage tissue in the central nervous system across a broad range of neuropathologies, including Alzheimer's disease, pain, Schizophrenia, and stroke. While the immune system plays an important role in contributing to brain damage produced by ischemia, the damaged brain, in turn, can exert a powerful immune-suppressive effect that promotes infections and threatens the survival of stroke patients. Recently the cholinergic anti-inflammatory pathway, in particular its modulation using α7-nicotinic acetylcholine receptor (α7-nAChR) ligands, has shown potential as a strategy to dampen the inflammatory response and facilitate functional recovery in stroke patients. Here we discuss the current literature on stroke-induced inflammation and the effects of α7-nAChR modulators on innate immune cells.
中风是导致死亡和长期残疾的主要原因之一,可用的治疗选择有限。炎症在包括阿尔茨海默病、疼痛、精神分裂症和中风在内的广泛神经病理学中,都会导致中枢神经系统组织损伤。虽然免疫系统在导致缺血性脑损伤中起重要作用,但受损的大脑反过来又会产生强大的免疫抑制作用,从而促进感染并威胁中风患者的生存。最近,胆碱能抗炎途径,特别是使用α7-烟碱型乙酰胆碱受体(α7-nAChR)配体对其进行调节,已显示出作为减轻炎症反应和促进中风患者功能恢复策略的潜力。在此,我们讨论了关于中风诱导炎症的当前文献以及α7-nAChR调节剂对先天免疫细胞的影响。