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绿茶多酚 (-)-表没食子儿茶素没食子酸酯可减少短暂性局灶性脑缺血后基质金属蛋白酶-9 的活性。

Green tea polyphenol (-)-epigallocatechin gallate reduces matrix metalloproteinase-9 activity following transient focal cerebral ischemia.

机构信息

Chronic Disease Research Center and Institute for Medical Science, School of Medicine, Keimyung University, Taegu 700-712, South Korea.

出版信息

J Nutr Biochem. 2010 Nov;21(11):1038-44. doi: 10.1016/j.jnutbio.2009.08.009. Epub 2009 Dec 4.

Abstract

Green tea polyphenol (-)-epigallocatechin gallate (EGCG) has been reported to reduce neuronal damage after cerebral ischemic insult. EGCG is known to reduce matrix metalloproteinase (MMP) activity. MMP can play an important role in the pathophysiology of neurological disorders including cerebral ischemia. The purpose of the current study was to investigate whether EGCG shows an inhibitory effect on MMP activity and neural tissue damage following transient focal cerebral ischemia. In the present study, C57BL/6 mice were subjected to 80 min of focal ischemia induced by middle cerebral artery occlusion (MCAO). Animals were killed 24 h after ischemia. EGCG (50 mg/kg) was administered intraperitoneally immediately after ischemia. Gelatin gel zymography showed an increase in the active form of MMP-9 after ischemia. EGCG reduced ischemia-induced up-regulation of the active form of MMP-9. In in situ zymography, EGCG reduced up-regulation of gelatinase activity induced by cerebral ischemia. Co-incubation with EGCG reduced gelatinase activity directly in postischemic brain section. In 2,3,5-triphenyltetrazolium chloride (TTC) assay, brain infarction was remarkable in the middle cerebral artery territory after focal cerebral ischemia. In EGCG-treated mice, infarct volume was significantly reduced compared with vehicle-treated mice. These results demonstrate that EGCG, a green tea polyphenol, may reduce up-regulation of MMP-9 activity and neuronal damage following transient focal cerebral ischemia. In addition to its antioxidant effect, MMP-9 inhibition might be a possible mechanism potentially involved in the neuroprotective effect of a green tea polyphenol, EGCG.

摘要

绿茶多酚(-)-表没食子儿茶素没食子酸酯(EGCG)已被报道可减少脑缺血后神经元损伤。已知 EGCG 可降低基质金属蛋白酶(MMP)的活性。MMP 在包括脑缺血在内的神经疾病的病理生理学中可发挥重要作用。本研究旨在探讨 EGCG 是否对短暂性局灶性脑缺血后 MMP 活性和神经组织损伤具有抑制作用。在本研究中,C57BL/6 小鼠通过大脑中动脉闭塞(MCAO)接受 80 分钟的局灶性缺血。缺血后 24 小时处死动物。缺血后立即腹腔内给予 EGCG(50mg/kg)。明胶凝胶酶谱显示缺血后 MMP-9 的活性形式增加。EGCG 降低了缺血诱导的 MMP-9 活性形式的上调。原位酶谱显示 EGCG 降低了脑缺血诱导的明胶酶活性的上调。与 EGCG 共孵育可直接降低缺血后脑切片中的明胶酶活性。在 2,3,5-三苯基四氮唑氯化物(TTC)测定中,局灶性脑缺血后大脑中动脉区域的脑梗死明显。在 EGCG 治疗的小鼠中,与载体治疗的小鼠相比,梗死体积明显减小。这些结果表明,绿茶多酚 EGCG 可能减少短暂性局灶性脑缺血后 MMP-9 活性和神经元损伤的上调。除了其抗氧化作用外,MMP-9 抑制可能是 EGCG 这种绿茶多酚发挥神经保护作用的潜在机制之一。

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