Effect of YM737, a new glutathione analogue, on ischemic brain edema.

O Gotoh, M Yamamoto, A Tamura, K Sano
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引用次数: 21

Abstract

We investigated the effect of YM737, a monoester of glutathione (GSH), on brain edema and GSH content after occlusion of a middle cerebral artery (MCA) in the rat. The drug possesses stronger radical scavenging activity than GSH itself, and is more effectively transported into cells. Hemispheric water, sodium, and potassium contents were determined at 2.5 and 24 hours after MCA occlusion. The animals received either YM737 or GSH immediately after occlusion. Cerebral GSH content was measured by HPLC after 2.5 hours of ischemia. The increases in water and sodium contents at 2.5 and 24 hours after MCA occlusion were significantly suppressed by YM737. GSH content decreased by 53% in the caudate, and by 22% in the cortex after ischemia. YM737 significantly ameliorated the GSH decrease in the caudate, while administration of GSH showed little effects on the ischemia-induced changes in water, sodium, and GSH contents. The result suggests the role of free radicals in the pathogenesis of ischemic brain edema.

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新型谷胱甘肽类似物YM737对缺血性脑水肿的影响。
我们研究了谷胱甘肽(GSH)单酯YM737对大脑中动脉(MCA)闭塞后大鼠脑水肿和GSH含量的影响。该药物比谷胱甘肽本身具有更强的自由基清除活性,并且更有效地转运到细胞中。在MCA闭塞后2.5和24小时测定半球水、钠和钾含量。动物在闭塞后立即接受YM737或GSH。缺血2.5 h后用高效液相色谱法测定脑GSH含量。在MCA闭塞后2.5和24小时,YM737显著抑制了水和钠含量的增加。脑缺血后尾状核GSH含量下降53%,皮层GSH含量下降22%。YM737显著改善尾状核中GSH的减少,而GSH对缺血引起的水、钠和GSH含量的变化影响不大。提示自由基在缺血性脑水肿发病机制中的作用。
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