Yasuda H, Kishiro K, Izumi N, Nakanishi M
J Neurochem. 1985 Jul;45(1):168-72. doi: 10.1111/j.1471-4159.1985.tb05489.x.
The mode of free fatty acid (FFA) liberation from the mouse brain during ischemia was investigated at various times after decapitation and under nizofenone treatment. Normal nonischemic brain FFAs consist mainly of palmitic acid (16:0), stearic acid (18:0), and oleic acid (18:1) with smaller amounts of arachidonic acid (20:4), docosahexaenoic acid (22:6), and others. Postdecapitative ischemia induced a rapid, biphasic release of 20:4 after a short lag of less than 30 s. The first phase showed a rapid 6.4-fold increase within 1 min of decapitation, followed by the second phase involving a slow release at less than one-fifth the rate of the first phase and lasting for at least 10 min. A similar, but not so marked, biphasic liberation was observed with 18:0. However, all of the other fatty acids (16:0, 18:1, 22:6, and others) were released only in a single phase at a slow rate. The time course for the rapid and specific liberation of 20:4 coincided with the time course for the decrease in brain ATP concentration during ischemia. Pretreatment of the animals with nizofenone resulted in a marked suppression of both FFA liberation and ATP depletion during ischemia. This suppression was particularly noteworthy with 20:4 and 18:0. The present study indicates that there is a specific and rapid liberation of 20:4 and 18:0 in a very early stage of ischemia and that this liberation seems to depend on availability of ATP in the brain. The physiological role of this transient 20:4 liberation during ischemia is discussed.
在断头后的不同时间以及尼唑苯酮治疗下,研究了缺血期间小鼠脑内游离脂肪酸(FFA)的释放模式。正常非缺血脑FFA主要由棕榈酸(16:0)、硬脂酸(18:0)和油酸(18:1)组成,含有少量花生四烯酸(20:4)、二十二碳六烯酸(22:6)等。断头后缺血在不到30秒的短暂延迟后诱导了20:4的快速双相释放。第一阶段在断头后1分钟内迅速增加6.4倍,随后第二阶段以低于第一阶段五分之一的速率缓慢释放,持续至少10分钟。18:0也观察到类似但不太明显的双相释放。然而,所有其他脂肪酸(16:0、18:1、22:6等)仅以缓慢的单阶段释放。缺血期间20:4快速特异性释放的时间进程与脑ATP浓度降低的时间进程一致。用尼唑苯酮预处理动物可显著抑制缺血期间的FFA释放和ATP消耗。这种抑制在20:4和18:0时尤为明显。本研究表明,在缺血的非常早期阶段,20:4和18:0存在特异性快速释放,并且这种释放似乎取决于脑内ATP的可用性。讨论了缺血期间这种短暂的20:4释放的生理作用。