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Ligustrazine reduces blood-brain barrier permeability in a rat model of focal cerebral ischemia and reperfusion

机译:川gust嗪降低大鼠局灶性脑缺血再灌注模型的血脑屏障通透性

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摘要

Ligustrazine, also known as 2,3,5,6-tetramethylpyrazine (TMP), one of the major active compounds of Ligusticum wallichii Franchat., has been shown to reduce neuroinflammation and protect neurons during cerebral ischemia/reperfusion injury. However, whether it reduces blood-brain barrier (BBB) permeability during ischemic stroke is unclear. The aim of the present study was to investigate the role that TMP plays in protecting the BBB integrity in ischemia/reperfusion injury and to investigate the relevant mechanisms involved. Rats received an intraperitoneal injection of 20 mg/kg TMP 15 min before the onset of ischemia, which was induced by middle cerebral artery occlusion. Infarct volume, neurological score, brain edema, BBB permeability and tight junction protein impairment were observed. The results showed that TMP reduced the neurological score and levels of brain infarction and edema. In addition, TMP significantly decreased BBB permeability and prevented the impairment of occludin and claudin-5, two tight junction protein components of the BBB, in rat brains with ischemia/reperfusion injury. In addition, the expression and activity of matrix metalloproteinases, enzymes responsible for the degradation of the extracellular matrix and tight junctions, were reduced in the rat brains by TMP treatment. These results combined suggest that TMP reduces BBB permeability as well as neuronal damage in focal cerebral ischemia/reperfusion injury in rats.
机译:川gust嗪,也被称为2,3,5,6-四甲基吡嗪(TMP),山茱Franc的主要活性化合物之一,已被证明可以减轻脑缺血/再灌注损伤中的神经炎症并保护神经元。然而,尚不清楚它是否降低缺血性中风期间的血脑屏障(BBB)通透性。本研究的目的是研究TMP在缺血/再灌注损伤中保护BBB完整性的作用,并研究所涉及的相关机制。大鼠在缺血发作前15分钟接受腹膜内注射20 mg / kg TMP,这是由于大脑中动脉闭塞引起的。观察梗死体积,神经学评分,脑水肿,血脑屏障通透性和紧密连接蛋白损伤。结果表明,TMP可降低神经系统评分以及脑梗死和水肿的水平。此外,TMP显着降低了缺血/再灌注损伤大鼠脑中BBB的通透性,并阻止了BBB的两个紧密连接蛋白成分occludin和claudin-5的损伤。此外,通过TMP处理可降低大鼠脑中基质金属蛋白酶(负责细胞外基质降解和紧密连接的酶)的表达和活性。这些结果综合表明,TMP降低了大鼠局灶性脑缺血/再灌注损伤中的BBB通透性以及神经元损害。

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