Robichaud L J, Marcoux F W
Department of Pharmacology, Parke-Davis Pharmaceutical Research Division, Warner Lambert Company, Ann Arbor, Michigan.
J Neurotrauma. 1990 Winter;7(4):193-206. doi: 10.1089/neu.1990.7.193.
Transcranial cold injury in rats and guinea pigs induced cerebral extravasation of albumin labeled with Evans blue dye or 125I, respective indicators of the area and amount of blood-brain barrier (BBB) disruption. Radioimmunoassay of brain extracts showed that cold injury induced leukotriene (LT)C4 in rat and guinea pig brains 15 min after injury. In guinea pigs, the LT synthesis inhibitor phenidone (30 mg/kg, i.p.) completely blocked cold-induced LTC4 in brain. Phenidone (30 and 100 mg/kg) also inhibited cerebral tissue accumulation of 125I-albumin and dye in rats and guinea pigs. Phenidone is reported to show antioxidant properties and selective lipoxygenase inhibition of arachidonic acid metabolism compared to cyclooxygenase inhibitors, meclofenamate sodium, and other nonsteroidal anti-inflammatory agents. Since several oxygen and hydroxyl radical scavengers and the cyclooxygenase inhibitor, meclofenamate sodium, did not inhibit protein extravasation, the findings support a role for LT as a mediator of cold-induced changes in BBB permeability in rats and guinea pigs and suggest that the inhibitory effects of phenidone on BBB permeability may be due to inhibition of LT production.
大鼠和豚鼠的经颅冷损伤导致用伊文思蓝染料或125I标记的白蛋白脑外渗,分别是血脑屏障(BBB)破坏面积和量的指标。对脑提取物的放射免疫分析表明,冷损伤在损伤后15分钟诱导大鼠和豚鼠脑中白三烯(LT)C4的产生。在豚鼠中,LT合成抑制剂非那吡啶(30毫克/千克,腹腔注射)完全阻断了脑中冷诱导的LTC4。非那吡啶(30和100毫克/千克)也抑制了大鼠和豚鼠脑中125I-白蛋白和染料的脑组织蓄积。据报道,与环氧化酶抑制剂甲氯芬那酸钠和其他非甾体抗炎药相比,非那吡啶具有抗氧化特性并能选择性抑制花生四烯酸代谢中的脂氧合酶。由于几种氧和羟基自由基清除剂以及环氧化酶抑制剂甲氯芬那酸钠均未抑制蛋白质外渗,这些发现支持LT作为大鼠和豚鼠冷诱导的BBB通透性变化的介质的作用,并表明非那吡啶对BBB通透性的抑制作用可能是由于抑制LT的产生。