LTC4/LTB4 alterations in rat forebrain ischemia and reperfusion and effects of AA-861, CV-3988.

Y Namura, H Shio, J Kimura
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引用次数: 18

Abstract

LTC4, which enhances vascular permeability and promotes tissue edema, and LTB4, which is a potent chemotactic and activating factor for leukocytes, were measured in rat brain after ischemia and several time periods of reperfusion. Forebrain ischemia was induced by 4-vessel occlusion. LTC4/LTB4 in the brain were measured by RIA. We also studied the effects of a 5-lipoxygenase inhibitor, AA-861 and a PAF antagonist, CV-3988 on LTC4/LTB4 concentrations. LTC4 in brain tissue increased during 30 min forebrain ischemia (p < 0.001). After reperfusion, LTC4 increased further, but at 15 min reperfusion LTC4 returned to the control level. Tissue levels of LTB4 in the brain increased during 30 min ischemia and remained high until 5 min after reperfusion (p < 0.01) returning at 15 min reperfusion to the control level. AA-861 inhibited elevation of LTC4/LTB4 in the reperfusion phase, but was not effective during ischemia. CV-3988 had a similar effect. LTC4 and LTB4 may be involved in the pathogenesis of ischemia brain edema and leukocyte infiltration. Further, PAF and LTs have many similarities of their pathophysiological properties, and may interact therefore in pathologic process.

LTC4/LTB4在大鼠前脑缺血再灌注中的改变及AA-861、CV-3988的影响。
在大鼠脑缺血和几段再灌注后,我们测量了增强血管通透性和促进组织水肿的LTC4和白细胞的有效趋化和激活因子LTB4。四支血管闭塞致前脑缺血。采用RIA法测定脑LTC4/LTB4。我们还研究了5-脂氧合酶抑制剂AA-861和PAF拮抗剂CV-3988对LTC4/LTB4浓度的影响。前脑缺血30min脑组织LTC4升高(p < 0.001)。再灌注后,LTC4进一步升高,但在再灌注15 min时,LTC4恢复到对照水平。脑组织LTB4水平在缺血30 min时升高,并维持在高水平直至再灌注后5 min (p < 0.01),再灌注15 min时恢复到对照水平。AA-861在再灌注期抑制LTC4/LTB4的升高,但在缺血期无效。CV-3988也有类似的效果。LTC4和LTB4可能参与脑缺血水肿和白细胞浸润的发病机制。此外,PAF和lt在病理生理特性上有许多相似之处,因此在病理过程中可能相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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