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原儿茶醛通过血脑屏障保护作用对大鼠脑缺血再灌注损伤的保护作用。

Protective Effect of Protocatechuic Aldehyde on Cerebral Ischemia/Reperfusion Injury in Rats through Blood-Brain Barrier Protection.

机构信息

Department of Pharmacology, Faculty of Chinese Materia Medic, Yunnan University of Chinese Medicine, Kunming, China.

Department of Kunming Health Professional College, Kunming, China.

出版信息

Bull Exp Biol Med. 2024 Oct;177(6):763-769. doi: 10.1007/s10517-024-06264-z. Epub 2024 Oct 26.

Abstract

Cerebral ischemia can lead to destruction of the blood-brain barrier (BBB), the main cause of cerebral edema and cerebral infarction. BBB damage is also one of the key factors affecting the result of drug therapy. We studied the protective effect of 5-day pretreatment with protocatechuic aldehyde (PAL) at doses of 10 and 20 mg/kg on BBB function and structure after middle cerebral artery occlusion/reperfusion (MCAO/R) in rats. The infarct volume, behavioral neurological deficit score, and Evans blue content in the brain were estimated. We also evaluated the content of nitric oxide (NO) and activities of inducible and neuronal NO synthases. Expression of aquaporin-4 (AQP-4), occludin, claudin-5, and MMP-3 in the brain tissues was estimated by Western blotting. The BBB ultrastructure was analyzed under an electron microscope. We revealed that PAL at both used doses significantly reduced the neurological deficit score, brain infarct volume, and Evans blue extravasation. Electron microscopy showed that PAL significantly improved the ultrastructure of BBB and alleviated its injury. Pretreatment with PAL increased expression of occludin and claudin-5 and reduced expression of AQP-4 and MMP-3. At the same time, the release of NO and activities of NO synthases were notably inhibited. Our results suggest that PAL can be a promising compound to attenuate cerebral ischemia resulting from occlusion/reperfusion injury via BBB protection.

摘要

脑缺血可导致血脑屏障(BBB)破坏,是脑水肿和脑梗死的主要原因。BBB 损伤也是影响药物治疗效果的关键因素之一。我们研究了原儿茶醛(PAL)在 10 和 20mg/kg 剂量下预处理 5 天对大鼠大脑中动脉闭塞/再灌注(MCAO/R)后 BBB 功能和结构的保护作用。评估了脑梗死体积、行为神经缺陷评分和脑内伊文思蓝含量。还评估了一氧化氮(NO)含量和诱导型和神经元型 NO 合酶的活性。通过 Western blot 评估脑组织中水通道蛋白-4(AQP-4)、闭合蛋白、闭合蛋白-5 和基质金属蛋白酶-3 的表达。在电子显微镜下分析 BBB 的超微结构。结果表明,两种剂量的 PAL 均显著降低了神经缺陷评分、脑梗死体积和伊文思蓝渗出量。电镜显示 PAL 显著改善了 BBB 的超微结构并减轻了其损伤。PAL 预处理增加了闭合蛋白和闭合蛋白-5 的表达,减少了 AQP-4 和 MMP-3 的表达。同时,显著抑制了 NO 的释放和 NO 合酶的活性。我们的结果表明,PAL 可能是一种有前途的化合物,可通过 BBB 保护来减轻闭塞/再灌注损伤引起的脑缺血。

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