Mabe H, Nagai H, Suzuka T
Department of Neurosurgery, Nagoya City University Medical School, Japan.
Neurol Res. 1990 Sep;12(3):165-8. doi: 10.1080/01616412.1990.11739937.
It has been postulated that lipoxygenase metabolites of arachidonic acid play a role in the pathogenesis of cerebral ischaemia. Severe forebrain ischaemia in rats was induced by four-vessel occlusion with mild hypotension. After 30 min of ischaemia, circulation was restored by removing the arterial clamps and increasing blood pressure to preischaemic levels. During 30 min of cerebral ischaemia, free arachidonic acid increased by approximately 8.5 times compared with the preischaemic level. This accumulation was reversed within 60 min of reperfusion. The concentration of leukotriene C4 in brain tissue increased significantly during reperfusion: treatment with a 5-lipoxygenase inhibitor, AA-861, decreased the increase of brain water content associated with reperfusion. This study demonstrated that the increased arachidonic acid resulting from cerebral ischaemia in rats is metabolized to leukotrienes via the lipoxygenase pathway once circulation is restored, and these leukotrienes may play some role in the development of postischaemic cerebral oedema.
据推测,花生四烯酸的脂氧合酶代谢产物在脑缺血的发病机制中起作用。通过四血管闭塞并伴有轻度低血压诱导大鼠严重的前脑缺血。缺血30分钟后,通过移除动脉夹并将血压升高至缺血前水平来恢复循环。在脑缺血的30分钟内,游离花生四烯酸与缺血前水平相比增加了约8.5倍。这种积累在再灌注60分钟内逆转。脑组织中白三烯C4的浓度在再灌注期间显著增加:用5-脂氧合酶抑制剂AA-861治疗可减少与再灌注相关的脑含水量增加。本研究表明,大鼠脑缺血产生的花生四烯酸增加在循环恢复后通过脂氧合酶途径代谢为白三烯,并且这些白三烯可能在缺血后脑水肿的发展中起一定作用。