Bradykinin postconditioning protects rat hippocampal neurons after restoration of spontaneous circulation following cardiac arrest via activation of the AMPK/mTOR signaling pathway  

作　　者：Shi-Rong Lin Qing-Ming Lin Yu-Jia Lin Xin Qian Xiao-Ping Wang Zheng Gong Feng Chen Bin Song 

机构地区：[1]Provincial College of Clinical Medicine,Fujian Medical University,Fuzhou,Fujian Province,China [2]Department of Emergency,Fujian Provincial Hospital South Branch,Fuzhou,Fujian Province,China [3]Department of Emergency,Fujian Provincial Hospital,Fuzhou,Fujian Province,China [4]Fujian Emergency Medical Center,Fuzhou,Fujian Province,China [5]Fujian Provincial Key Laboratory of Emergency Medicine,Fuzhou,Fujian Province,China [6]Department of Human Anatomy,School of Basic Medical Sciences,Fujian Medical University,Fuzhou,Fujian Province,China [7]Key Laboratory of Brain Aging and Neurodegenerative Diseases of Fujian Province,Fuzhou,Fujian Province,China [8]Laboratory of Clinical Applied Anatomy,Fujian Medical University,Fuzhou,Fujian Province,China

出　　处：《Neural Regeneration Research》2022年第10期2232-2237,共6页中国神经再生研究（英文版）

基　　金：supported by the Fujian Provincial Health Technology Project of China,No.2018-CX-16;Fujian Provincial Hospital Flint Fund Project,No.2020HSJJ17(both to SRL).

摘　　要：Bradykinin(BK)is an active component of the kallikrein-kinin system that has been shown to have cardioprotective and neuroprotective effects.We previously showed that BK postconditioning strongly protects rat hippocampal neurons upon restoration of spontaneous circulation(ROSC)after cardiac arrest.However,the precise mechanism underlying this process remains poorly understood.In this study,we treated a rat model of ROSC after cardiac arrest(induced by asphyxiation)with 150μg/kg BK via intraperitoneal injection 48 hours after ROSC following cardiac arrest.We found that BK postconditioning effectively promoted the recovery of rat neurological function after ROSC following cardiac arrest,increased the amount of autophagosomes in the hippocampal tissue,inhibited neuronal cell apoptosis,up-regulated the expression of autophagy-related proteins LC3 and NBR1 and down-regulated p62,inhibited the expression of the brain injury marker S100βand apoptosis-related protein caspase-3,and affected the expression of adenosine monophosphate-activated protein kinase/mechanistic target of rapamycin pathway-related proteins.Adenosine monophosphate-activated protein kinase inhibitor compound C clearly inhibited BK-mediated activation of autophagy in rats after ROSC following cardiac arrest,which aggravated the injury caused by ROSC.The mechanistic target of rapamycin inhibitor rapamycin enhanced the protective effects of BK by stimulating autophagy.Our findings suggest that BK postconditioning protects against injury caused by ROSC through activating the adenosine monophosphate-activated protein kinase/mechanistic target of the rapamycin pathway.

关 键 词：autophagy BRADYKININ cardiac arrest cardiopulmonary resuscitation compound C hippocampus neuron rapamycin restoration of spontaneous circulation 

分 类 号：R541.78[医药卫生—心血管疾病]