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丹酚酸 A 通过抑制 MMP-9 和抗炎作用保护血脑屏障,减轻缺血再灌注诱导的大鼠脑损伤。

Salvianolic acid A attenuates ischemia reperfusion induced rat brain damage by protecting the blood brain barrier through MMP-9 inhibition and anti-inflammation.

机构信息

Beijing Key Laboratory of Drug Target Identification and Drug Screening, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China.

Department of Neuroimmunopharmacology, Beijing Institute of Pharmacology and Toxicology, State Key Laboratory of Toxicology and Medical Countermeasures, Beijing 100850, China.

出版信息

Chin J Nat Med. 2018 Mar;16(3):184-193. doi: 10.1016/S1875-5364(18)30046-3.

Abstract

Salvianolic acid A (SAA) is a water-soluble component from the root of Salvia Miltiorrhiza Bge, a traditional Chinese medicine, which has been used for the treatment of cerebrovascular diseases for centuries. The present study aimed to determine the brain protective effects of SAA against cerebral ischemia reperfusion injury in rats, and to figure out whether SAA could protect the blood brain barrier (BBB) through matrix metallopeptidase 9 (MMP-9) inhibition. A focal cerebral ischemia reperfusion model was induced by middle cerebral artery occlusion (MCAO) for 1.5-h followed by 24-h reperfusion. SAA was administered intravenously at doses of 5, 10, and 20 mg·kg. SAA significantly reduced the infarct volumes and neurological deficit scores. Immunohistochemical analyses showed that SAA treatments could also improve the morphology of neurons in hippocampus CA1 and CA3 regions and increase the number of neurons. Western blotting analyses showed that SAA downregulated the levels of MMP-9 and upregulated the levels of tissue inhibitor of metalloproteinase 1 (TIMP-1) to attenuate BBB injury. SAA treatment significantly prevented MMP-9-induced degradation of ZO-1, claudin-5 and occludin proteins. SAA also prevented cerebral NF-κB p65 activation and reduced inflammation response. Our results suggested that SAA could be a promising agent to attenuate cerebral ischemia reperfusion injury through MMP-9 inhibition and anti-inflammation activities.

摘要

丹酚酸 A(SAA)是丹参根部的一种水溶性成分,丹参是一种中药,几个世纪以来一直用于治疗脑血管疾病。本研究旨在确定 SAA 对大鼠脑缺血再灌注损伤的脑保护作用,并确定 SAA 是否可以通过基质金属蛋白酶 9(MMP-9)抑制来保护血脑屏障(BBB)。通过大脑中动脉闭塞(MCAO)诱导 1.5 小时的局灶性脑缺血再灌注模型,然后再灌注 24 小时。SAA 以 5、10 和 20mg·kg 的剂量静脉给药。SAA 显著减少梗死体积和神经功能缺损评分。免疫组织化学分析表明,SAA 治疗还可以改善海马 CA1 和 CA3 区神经元的形态,并增加神经元数量。Western blot 分析表明,SAA 下调 MMP-9 水平,上调组织金属蛋白酶抑制剂 1(TIMP-1)水平,从而减轻 BBB 损伤。SAA 处理还可以防止 MMP-9 诱导的 ZO-1、claudin-5 和 occludin 蛋白降解。SAA 还可以防止脑 NF-κB p65 激活并减轻炎症反应。我们的研究结果表明,SAA 通过 MMP-9 抑制和抗炎活性可能是一种有前途的减轻脑缺血再灌注损伤的药物。

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