Protective effects of low-intensity pulsed ultrasound (LIPUS) against cerebral ischemic stroke in mice by promoting brain vascular remodeling via the inhibition of ROCK1/p-MLC2 signaling pathway

低强度脉冲超声 岩石1 医学 脑血流 脑循环 岩石2 冲程(发动机) 信号转导 内科学 细胞生物学 激酶 Rho相关蛋白激酶 生物 蛋白激酶A 超声波 放射科 工程类 机械工程 治疗性超声
作者
Rong Chen,Wei Du,Xiao Zhang,Renhao Xu,Wei Jiang,Cong Zhang,Yi Yang,Huiran Zhang,Xiaoli Xie,Degang Song,Yi Yuan,Xiangjian Zhang
出处
期刊:Cerebral Cortex [Oxford University Press]
卷期号:33 (22): 10984-10996 被引量:6
标识
DOI:10.1093/cercor/bhad330
摘要

Vascular remodeling is essential for patients with cerebral ischemic stroke (CIS). Our previous study proved that low-intensity pulsed ultrasound (LIPUS) could increase cortical hemodynamics. However, the effects and mechanisms of LIPUS on cerebral vascular remodeling after CIS are still unknown. In this study, we applied LIPUS to the mouse brain at 0.5 h after distal middle cerebral artery occlusion (dMCAO) and subsequently daily for a stimulation time of 30 min. Results showed that compared with the dMCAO group, LIPUS markedly increased cerebral blood flow (CBF), reduced brain swelling, and improved functional recovery at day 3 after CIS. LIPUS promoted leptomeningeal vasculature remodeling, enlarged vascular diameter, and increased the average vessel length and density at day 3 after CIS. Proteomic analysis highlighted that LIPUS mainly participated in the regulation of actin cytoskeleton pathway. Rho kinase 1 (ROCK1) was downregulated by LIPUS and participated in regulation of actin cytoskeleton. Subsequently, we verified that ROCK1 was mainly expressed in pericytes. Furthermore, we demonstrated that LIPUS inhibited ROCK1/p-MLC2 signaling pathway after CIS, which had positive effects on vascular remodeling and cerebral blood circulation. In conclusion, our preliminary study revealed the vascular remodeling effects and mechanism of LIPUS in CIS, provided evidence for potential clinical application of LIPUS.
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