Department of Physiology and Graduate School (Neuroscience Program), Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand ; Integrative Complementary Alternative Medicine Research and Development Center, Khon Kaen University, Khon Kaen 40002, Thailand.
Integrative Complementary Alternative Medicine Research and Development Center, Khon Kaen University, Khon Kaen 40002, Thailand ; Department of Physiology, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand.
Oxid Med Cell Longev. 2013;2013:951415. doi: 10.1155/2013/951415. Epub 2013 Dec 3.
The protection against ischemic stroke is still required due to the limitation of therapeutic efficacy. Based on the role of oxidative stress in stroke pathophysiology, we determined whether Moringa oleifera, a plant possessing potent antioxidant activity, protected against brain damage and oxidative stress in animal model of focal stroke. M. oleifera leaves extract at doses of 100, 200 and 400 mg·kg(-1) was orally given to male Wistar rats (300-350 g) once daily at a period of 2 weeks before the occlusion of right middle cerebral artery (Rt.MCAO) and 3 weeks after Rt.MCAO. The determinations of neurological score and temperature sensation were performed every 7 days throughout the study period, while the determinations of brain infarction volume, MDA level, and the activities of SOD, CAT, and GSH-Px were performed 24 hr after Rt.MCAO. The results showed that all doses of extract decreased infarction volume in both cortex and subcortex. The protective effect of medium and low doses of extract in all areas occurred mainly via the decreased oxidative stress. The protective effect of the high dose extract in striatum and hippocampus occurred via the same mechanism, whereas other mechanisms might play a crucial role in cortex. The detailed mechanism required further exploration.
由于治疗效果的限制,仍然需要预防缺血性中风。基于氧化应激在中风病理生理学中的作用,我们确定了具有强大抗氧化活性的辣木是否可以预防局灶性中风动物模型中的脑损伤和氧化应激。辣木叶提取物以 100、200 和 400mg·kg(-1) 的剂量每天口服给予雄性 Wistar 大鼠(300-350g),在右侧大脑中动脉闭塞(Rt.MCAO)前 2 周和 Rt.MCAO 后 3 周进行一次。在整个研究期间,每 7 天进行一次神经评分和温度感觉测定,而在 Rt.MCAO 后 24 小时进行脑梗死体积、MDA 水平以及 SOD、CAT 和 GSH-Px 活性的测定。结果表明,提取物的所有剂量均减少了皮质和皮质下的梗死体积。中低剂量提取物在所有区域的保护作用主要通过降低氧化应激来实现。高剂量提取物在纹状体和海马中的保护作用通过相同的机制发生,而其他机制可能在皮质中发挥关键作用。详细的机制需要进一步探索。