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作 者:Hong-Bin Lin Guan-Shan Wei Feng-Xian Li Wen-Jing Guo Pu Hong Ya-Qian Weng Qian-Qian Zhang Shi-Yuan Xu Wen-Bin Liang Zhi-Jian You Hong-Fei Zhang
机构地区:[1]Department of Anesthesiology,Zhujiang Hospital of Southern Medical University,Guangzhou 510220,China [2]Department of Anesthesiology,Shenzhen SAMII Medical Center,Shenzhen 518118,China [3]Department of Anesthesiology,The Second Affiliated Hospital,Shantou University Medical College,Shantou 515041,China [4]University of Ottawa Heart Institute and Department of Cellular and Molecular Medicine,University of Ottawa,Ontario,K1N,Canada
出 处:《Neuroscience Bulletin》2020年第9期1035-1045,共11页神经科学通报(英文版)
基 金:supported by grants from the National Natural Science Foundation of China (81771232 and 81974192);the Natural Science Foundation of Guangdong Province,China (2019A1515010654)。
摘 要:Ischemic stroke is one of the leading causes of death worldwide.In the post-stroke stage,cardiac dysfunction is common and is known as the brain-heart interaction.Diabetes mellitus worsens the post-stroke outcome.Stroke-induced systemic inflammation is the major causative factor for the sequential complications,but the mechanism underlying the brain-heart interaction in diabetes has not been clarified.The NLRP3(NLR pyrin domain-containing 3) inflammasome,an important component of the inflammation after stroke,is mainly activated in M1-polarized macrophages.In this study,we found that the cardiac dysfunction induced by ischemic stroke is more severe in a mouse model of type 2 diabetes.Meanwhile,M1-polarized macrophage infiltration and NLRP3 inflammasome activation increased in the cardiac ventricle after diabetic stroke.Importantly,the NLRP3 inflammasome inhibitor CY-09 restored cardiac function,indicating that the Ml-polarized macrophage-NLRP3 inflammasome activation is a pathway underlying the brain-heart interaction after diabetic stroke.
关 键 词:Ischemic stroke Diabetes mellitus Cardiac dysfunction NLRP3 inflammasome MACROPHAGE
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