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The effects of calcitonin gene-related peptide on bFGF and AQP4 expression after focal cerebral ischemia reperfusion in rats.

机译:降钙素基因相关肽对大鼠局灶性脑缺血再灌注后bFGF和AQP4表达的影响。

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The aim of this study was to investigate whether calcitonin gene-related peptide (CGRP) administration could produce neuroprotective effects after brain ischemia reperfusion in rats. Brain ischemia reperfusion injury was induced by a 2-hour left middle cerebral artery occlusion (MCAO) using an intraluminal filament, followed by 46hours of reperfusion. CGRP (1 microg/ml) at the dose of 3 microg/kg, i.p., was administered at the beginning of reperfusion. Saline (3 ml/kg body weight) treated animals were used as control. Sham-operated animals were also used. Subsequently, 48 hours after MCAO, infarct volume, histological alterations, based fibroblast growth factor (bFGF) and aquaporin-4 (AQP4) expression were examined. The results showed that CGRP could significantly decrease infarct volume, improve brain tissue histological damage, promote bFGF expression and inhibit AQP4 expression after brain ischemia reperfusion injury. The results suggested that the neuroprotective effects of CGRP may be mediated by promoting bFGF expression and inhibiting AQP4 expression. The spatial and temporal distribution of molecules involved in the ischemic cascade by CGRP administration should be further studied.
机译:这项研究的目的是研究降钙素基因相关肽(CGRP)的给药是否可以在大鼠脑缺血再灌注后产生神经保护作用。脑缺血再灌注损伤是通过使用腔内灯丝2小时左大脑中动脉闭塞(MCAO)引起的,然后再进行46小时再灌注。在再灌注开始时以3微克/千克的剂量腹膜内注射CGRP(1微克/毫升)。盐水(3ml / kg体重)处理的动物用作对照。还使用了假手术的动物。随后,在MCAO后48小时,检查梗塞体积,组织学改变,基础成纤维细胞生长因子(bFGF)和水通道蛋白4(AQP4)的表达。结果表明,CGRP可以显着减少脑缺血再灌注损伤后的梗塞体积,改善脑组织的组织学损伤,促进bFGF表达并抑制AQP4表达。结果表明,CGRP的神经保护作用可能通过促进bFGF表达和抑制AQP4表达来介导。应进一步研究通过CGRP给药参与缺血级联反应的分子的时空分布。

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