Huo Jun-Yu, Jiang Wan-Ying, Lyu Yi-Ting, Zhu Lin, Liu Hui-Hui, Chen Yuan-Yuan, Chen Meng, Geng Jie, Jiang Zhi-Xin, Shan Qi-Jun
Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Front Cardiovasc Med. 2021 Apr 26;8:650140. doi: 10.3389/fcvm.2021.650140. eCollection 2021.
The development of neuroinflammation deteriorates the prognosis of myocardial infarction (MI). We aimed to investigate the effect of renal denervation (RDN) on post-MI neuroinflammation in rats and the related mechanisms. Male adult Sprague-Dawley rats were subjected to sham or ligation of the left anterior descending coronary artery to induce MI. One week later, the MI rats received a sham or RDN procedure. Their cardiac functions were analyzed by echocardiography, and their intestinal structures, permeability, and inflammatory cytokines were tested. The intestinal microbiota were characterized by 16S rDNA sequencing. The degrees of neuroinflammation in the brains of rats were analyzed for microglia activation, inflammatory cytokines, and inflammation-related signal pathways. In comparison with the Control rats, the MI rats exhibited impaired cardiac functions, intestinal injury, increased intestinal barrier permeability, and microbial dysbiosis, accompanied by increased microglia activation and pro-inflammatory cytokine levels in the brain. A RDN procedure dramatically decreased the levels of renal and intestinal sympathetic nerve activity, improved cardiac functions, and mitigated the MI-related intestinal injury and neuroinflammation in the brain of MI rats. Interestingly, the RDN procedure mitigated the MI-increased intestinal barrier permeability and pro-inflammatory cytokines and plasma LPS as well as ameliorated the gut microbial dysbiosis in MI rats. The protective effect of RDN was not significantly affected by treatment with intestinal alkaline phosphatase but significantly reduced by L-phenylalanine treatment in MI rats. RDN attenuated the neuroinflammation in the brain of MI rats, associated with mitigating the MI-related intestinal injury.
神经炎症的发展会使心肌梗死(MI)的预后恶化。我们旨在研究肾去神经支配(RDN)对大鼠心肌梗死后神经炎症的影响及其相关机制。成年雄性Sprague-Dawley大鼠接受假手术或结扎左冠状动脉前降支以诱导心肌梗死。一周后,心肌梗死大鼠接受假手术或肾去神经支配手术。通过超声心动图分析其心脏功能,并检测其肠道结构、通透性和炎性细胞因子。通过16S rDNA测序对肠道微生物群进行表征。分析大鼠大脑中神经炎症的程度,包括小胶质细胞活化、炎性细胞因子和炎症相关信号通路。与对照大鼠相比,心肌梗死大鼠表现出心脏功能受损、肠道损伤、肠道屏障通透性增加和微生物群落失调,同时大脑中小胶质细胞活化增加和促炎细胞因子水平升高。肾去神经支配手术显著降低了肾和肠道交感神经活动水平,改善了心脏功能,并减轻了心肌梗死大鼠大脑中与心肌梗死相关的肠道损伤和神经炎症。有趣的是,肾去神经支配手术减轻了心肌梗死增加的肠道屏障通透性、促炎细胞因子和血浆脂多糖,并改善了心肌梗死大鼠的肠道微生物群落失调。肾去神经支配的保护作用在心肌梗死大鼠中不受肠道碱性磷酸酶治疗的显著影响,但L-苯丙氨酸治疗可使其显著降低。肾去神经支配减轻了心肌梗死大鼠大脑中的神经炎症,这与减轻心肌梗死相关的肠道损伤有关。