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首页> 外文期刊>European review for medical and pharmacological sciences. >Histamine H3 receptor antagonist Clobenpropit protects propofol-induced apoptosis of hippocampal neurons through PI3K/AKT pathway
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Histamine H3 receptor antagonist Clobenpropit protects propofol-induced apoptosis of hippocampal neurons through PI3K/AKT pathway

机译:组胺H3受体拮抗剂Clobenpropit通过PI3K / AKT途径保护异丙酚诱导的海马神经元凋亡

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OBJECTIVE: The aim of the study was to explore whether histamine H3 receptor antagonist Clobenpropit could protect propofol-induced neurotoxicity in hippocampal neurons. MATERIALS AND METHODS: Hippocampal neurons were extracted from neonatal rats and induced with propofol. MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assay was performed to detect apoptotic rate of neurons. Western blot was conducted to detect protein levels of cleaved-caspase-3 and Bax/Bcl2. After LY294002 treatment, the PI3K pathway antagonist was applied in neurons, protein levels of cleaved-caspase-3 and Bax/Bcl2 were detected by Western blot as well. RESULTS: Propofol treatment remarkably induced neuronal apoptosis. Clobenpropit alleviated cell apoptosis induced by propofol. Protein expressions of cleaved-caspase-3 and Bax/Bcl2 were remarkably downregulated in neurons treated with Clobenpropit. LY294002 induction remarkably reverses the protective role of Clobenpropit in neuronal apoptosis, manifesting as downregulated PI3K and p-AKT after LY294002 treatment. CONCLUSIONS: Clobenpropit protects propofol-induced neuronal apoptosis through activating PI3K/AKT pathway.
机译:目的:本研究旨在探讨组胺H3受体拮抗剂Clobenpropit是否可以保护异丙酚对海马神经元的神经毒性。材料与方法:从新生大鼠中提取海马神经元,并用异丙酚诱导。进行MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑鎓)测定以检测神经元的凋亡率。进行了蛋白质印迹法以检测裂解的caspase-3和Bax / Bcl2的蛋白质水平。 LY294002处理后,将PI3K途径拮抗剂应用于神经元,同时通过Western blot检测caspase-3和Bax / Bcl2的蛋白水平。结果:异丙酚治疗可明显诱导神经元凋亡。 Clobenpropit减轻了异丙酚诱导的细胞凋亡。在用Clobenpropit处理的神经元中,裂解的caspase-3和Bax / Bcl2的蛋白表达显着下调。 LY294002诱导显着逆转Clobenpropit在神经元凋亡中的保护作用,表现为LY294002处理后PI3K和p-AKT的表达下调。结论:Clobenpropit通过激活PI3K / AKT途径保护异丙酚诱导的神经元凋亡。

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