Hattori T, Sakai N, Yamada H, Kameyama Y, Nozawa Y
No To Shinkei. 1985 Apr;37(4):377-83.
It is generally known that free fatty acids (FFA) are liberated from membrane phospholipids in the brain tissue during the early period of ischemia. However, the precise mechanism of FFA liberation from phospholipids is still unclear, even though it is a central topic of neurosurgery. As an initial step toward a better understanding of the molecular mechanism, we have investigated the effects of global ischemia upon brain lipid metabolism. Brain ischemia was evoked by rat decapitation without anesthesia. Removed brains were incubated for 1, 5, 15 or 30 min at 37 degrees C and then quickly frozen in liquid nitrogen. After extraction of total lipids from the brains by Bligh & Dyer's method, the compositions of neutral lipids and phospholipids were analyzed by thin-layer and gas-liquid chromatography. For assaying deacylating enzyme (phospholipase A) activity, the brain homogenate was used as a crude enzyme. The reaction mixture including radioactive substrate, buffer (pH 7.3 & 4.0) and enzyme was incubated for 1 hour at 37 degrees C. Lipids were extracted from reaction mixture and separated by TLC. The enzyme activity was estimated by measuring the radioactivity in FFA or lysophosphatidylcholine liberated from L-alpha-di [1-14C] palmitoyl phosphatidylcholine. The reaction mixture for the assay of reacylating enzyme (acyl CoA: lysophospholipid acyltransferase) activity, contained acyl CoA, lysophosphatidylcholine, DTNB and microsomes, and the enzyme activity was determined by the amount of released CoA-SH detected spectrophotometrically. The results demonstrated that FFA, either unsaturated or saturated, rapidly accumulated in the brain during the early period of ischemia. Di-acylglycerols were also produced in the ischemic brain.(ABSTRACT TRUNCATED AT 250 WORDS)
众所周知,在缺血早期,脑组织中的膜磷脂会释放出游离脂肪酸(FFA)。然而,尽管FFA从磷脂中释放的确切机制是神经外科的核心课题,但仍不清楚。作为更好地理解分子机制的第一步,我们研究了全脑缺血对脑脂质代谢的影响。通过在无麻醉的情况下断头诱发大鼠脑缺血。取出的大脑在37℃下孵育1、5、15或30分钟,然后迅速在液氮中冷冻。通过布莱-戴尔法从大脑中提取总脂质后,用薄层色谱法和气液色谱法分析中性脂质和磷脂的组成。为了测定脱酰酶(磷脂酶A)的活性,将脑匀浆用作粗酶。将包含放射性底物、缓冲液(pH 7.3和4.0)和酶的反应混合物在37℃下孵育1小时。从反应混合物中提取脂质并通过薄层色谱法分离。通过测量从L-α-二[1-14C]棕榈酰磷脂酰胆碱释放的FFA或溶血磷脂酰胆碱中的放射性来估计酶活性。用于测定再酰化酶(酰基辅酶A:溶血磷脂酰基转移酶)活性的反应混合物包含酰基辅酶A、溶血磷脂酰胆碱、二硫代硝基苯甲酸和微粒体,酶活性通过分光光度法检测释放的辅酶A-SH的量来确定。结果表明,在缺血早期,不饱和或饱和的FFA在脑中迅速积累。缺血脑中也产生了二酰甘油。(摘要截短于250字)