Cho Jae-Yong, Kim In-Soo, Jang Young-Ho, Kim Ae-Ra, Lee Seong-Ryong
Department of Anesthesiology, School of Medicine, Keimyung University, Taegu, South Korea.
Neurosci Lett. 2006 Sep 1;404(3):330-5. doi: 10.1016/j.neulet.2006.06.010. Epub 2006 Jun 27.
Previous studies have demonstrated that quercetin, a bioflavonoid shows the inhibitory effect against ischemia and reperfusion-induced injury in various tissues including neural tissue. Quercetin is also reported to have an inhibitory effect against matrix metalloproteinases (MMPs). Because MMPs are known to play a main role in the pathophysiology of brain ischemic insult, their mechanisms of possible protective effect of quercetin against brain ischemia remain to be clarified. In the present study, C57BL/6 mice were subjected to 20 min transient global brain ischemia. Cerebral blood flow was monitored by laser doppler flowmeter. Animals were sacrificed 72 h after ischemia. Quercetin (50 mg/kg, dissolved in saline) was intraperitoneally administered to mice at 30 min before and immediately after ischemia and from the second day, quercetin was then administered once daily until sacrifice. The present study was undertaken to test the effect of quercetin on neuronal damage after transient cerebral ischemia. Neuronal damages were remarkable in the medial portion of CA1 and CA2 areas after ischemic insult. In quercetin-treated mice, delayed neuronal damage was significantly decreased compared with vehicle-treated mice. Mice treated with quercetin showed attenuated brain MMP-9 activity. Gelatin gel zymography showed an induction of MMP-9 protein after ischemia. Quercetin significantly inhibited ischemia-induced elevation of MMP-9. In situ zymography showed elevations in gelatinase activities after brain ischemia. Quercetin also inhibited TdT-mediated dUTP nick end labeling (TUNEL) staining in CA1 and CA2 areas. These results demonstrate that quercetin, a natural flavonoid reduces global ischemia-induced neuronal damage through inhibition of MMP-9 activity.
先前的研究表明,生物类黄酮槲皮素对包括神经组织在内的各种组织的缺血再灌注损伤具有抑制作用。据报道,槲皮素对基质金属蛋白酶(MMPs)也有抑制作用。由于已知MMPs在脑缺血损伤的病理生理学中起主要作用,槲皮素对脑缺血可能的保护作用机制仍有待阐明。在本研究中,C57BL/6小鼠经历了20分钟的短暂全脑缺血。用激光多普勒血流仪监测脑血流量。缺血72小时后处死动物。在缺血前30分钟和缺血后立即给小鼠腹腔注射槲皮素(50mg/kg,溶于生理盐水),从第二天起,每天注射一次槲皮素直至处死。本研究旨在测试槲皮素对短暂性脑缺血后神经元损伤的影响。缺血损伤后,CA1和CA2区域的内侧部分神经元损伤明显。与载体处理的小鼠相比,槲皮素处理的小鼠延迟性神经元损伤明显减少。用槲皮素处理的小鼠脑MMP-9活性减弱。明胶酶谱显示缺血后MMP-9蛋白的诱导。槲皮素显著抑制缺血诱导MMP-9的升高。原位酶谱显示脑缺血后明胶酶活性升高。槲皮素还抑制CA1和CA2区域的TdT介导的dUTP缺口末端标记(TUNEL)染色。这些结果表明,天然黄酮类化合物槲皮素通过抑制MMP-9活性减少全脑缺血诱导的神经元损伤。