Department of Nutritional Sciences, Faculty of Medicine, University of Toronto, Toronto, Canada.
J Lipid Res. 2010 Mar;51(3):535-43. doi: 10.1194/jlr.M000786. Epub 2009 Aug 6.
Previous studies have infused radiolabeled arachidonic acid (AA) into rat brains and followed AA esterification into phospholipids for up to 24 h; however, the half-life of AA in rat brain phospholipids is unknown. Eighteen day old rats were fed either an n-3 PUFA adequate or deprived diet for 15 weeks. Following the 15 weeks, 40 microCi of [(3)H] AA was injected intracerebroventricularly into the right lateral ventricle using stereotaxic surgery and returned to their dietary treatment. From 4-120 days after [(3)H] AA administration, brains were collected for chemical analyses. The half-life of AA in rat brain phospholipids was 44 +/- 4 days for the n-3 PUFA adequate group and 46 +/- 4 days for the n-3 PUFA deprived group, which closely approximates the predicted half-life previously reported, based on the rate of entry from the plasma unesterified pool, suggesting the plasma unesterified pool is a major contributor to brain uptake of AA. Furthermore, unlike a previous report in which the half-life of brain phospholipid docosahexaenoic acid (DHA) was increased in n-3 PUFA deprived rats, n-3 PUFA deprivation did not significantly alter the AA half-life, suggesting different mechanisms exist to maintain brain concentrations of AA and DHA.
先前的研究已经将放射性标记的花生四烯酸(AA)注入大鼠大脑,并在长达 24 小时内追踪 AA 酯化到磷脂中;然而,AA 在大鼠脑磷脂中的半衰期尚不清楚。18 天龄的大鼠接受 n-3PUFA 充足或缺乏饮食 15 周。在 15 周后,使用立体定向手术将 40 微 Ci 的 [(3)H]AA 注入右侧侧脑室。从 [(3)H]AA 给药后 4-120 天,收集大脑进行化学分析。n-3PUFA 充足组和 n-3PUFA 缺乏组大鼠脑磷脂中 AA 的半衰期分别为 44 +/- 4 天和 46 +/- 4 天,与先前基于从血浆未酯化池中进入的速度预测的半衰期非常接近,表明血浆未酯化池是 AA 进入大脑的主要贡献者。此外,与先前报道的 n-3PUFA 缺乏大鼠脑磷脂二十二碳六烯酸(DHA)半衰期延长的情况不同,n-3PUFA 缺乏并没有显著改变 AA 的半衰期,这表明存在不同的机制来维持大脑中 AA 和 DHA 的浓度。