Department of Anesthesiology, Qingdao Hospital, University of Health and Rehabilitation Sciences (Qingdao Municipal Hospital), Qingdao, 266071, China.
Department of Anesthesiology, Qingdao Municipal Hospital, Qingdao University, Qingdao, 266071, China.
Sci Rep. 2023 Sep 2;13(1):14450. doi: 10.1038/s41598-023-41766-2.
Cerebral ischemia is one of the leading causes of disability and mortality worldwide. Blood reperfusion of ischemic cerebral tissue may cause cerebral ischemia-reperfusion (IR) injury. In this study, a rat model of global cerebral I/R injury was established via Pulsinelli's four-vessel occlusion (4-VO) method. The liquid chromatography-tandem mass spectrometry (LC-MS/MS) and bioinformatics analysis were employed to examine the ipsilateral hippocampus proteome profiles of rats with/without MH (32 °C) treatment after IR injury. Totally 2 122 proteins were identified, among which 153 proteins were significantly changed associated with MH (n = 7 per group, fold change-1.5, p < 0.05). GO annotation of the differentially expressed proteins (DEPs) revealed that cellular oxidant detoxification, response to zinc ions, aging, oxygen transport, negative regulation of catalytic activity, response to hypoxia, regulation of protein phosphorylation, and cellular response to vascular endothelial growth factor stimulus were significantly enriched with MH treatment. The KEGG analysis indicated that metabolic pathways, thermogenesis, pathways of neurodegeneration, chemical carcinogenesis-reactive oxygen species, fluid shear stress and atherosclerosis, and protein processing in endoplasmic reticulum were significantly enriched with MH treatment. Importantly, changes in 16 DEPs were reversed by MH treatment. Among them, VCAM-1, S100A8, CaMKK2 and MKK7 were verified as potential markers associated with MH neuroprotection by Western blot analysis. This study is one of the first to investigate the neuroprotective effects of MH on the hippocampal proteome of experimental models of cerebral IR injury. These DEPs may be involved in the most fundamental molecular mechanisms of MH neuroprotection, and provide a scientific foundation for further promotion of reparative strategies in cerebral IR injury.
脑缺血是全球致残和致死的主要原因之一。缺血性脑组织的血液再灌注可能导致脑缺血再灌注(IR)损伤。在本研究中,通过 Pulsinelli 的四血管闭塞(4-VO)方法建立了大鼠全脑 I/R 损伤模型。采用液相色谱-串联质谱(LC-MS/MS)和生物信息学分析方法,检测了缺血再灌注损伤后接受 MH(32°C)治疗的大鼠和未接受 MH 治疗的大鼠(每组 7 只)对侧海马蛋白质组图谱。共鉴定出 2122 种蛋白质,其中 153 种蛋白质与 MH 相关的变化显著(n=7 只/组,倍数变化-1.5,p<0.05)。差异表达蛋白(DEPs)的 GO 注释表明,MH 处理后,细胞氧化剂解毒、对锌离子的反应、衰老、氧运输、催化活性的负调控、对缺氧的反应、蛋白质磷酸化的调节和血管内皮生长因子刺激的细胞反应显著富集。KEGG 分析表明,代谢途径、发热、神经退行性变途径、化学致癌作用-活性氧、切应力和动脉粥样硬化以及内质网蛋白质加工在 MH 处理后显著富集。重要的是,MH 处理逆转了 16 个 DEP 的变化。其中,通过 Western blot 分析,验证 VCAM-1、S100A8、CaMKK2 和 MKK7 是与 MH 神经保护相关的潜在标志物。本研究是首次研究 MH 对实验性脑 IR 损伤模型海马蛋白质组的神经保护作用。这些 DEPs 可能参与了 MH 神经保护的最基本的分子机制,为进一步促进脑 IR 损伤的修复策略提供了科学依据。