Ghersi-Egea J F, Leninger-Muller B, Suleman G, Siest G, Minn A
Centre du medicament, URACNRS 597, Universite de Nancy I, France.
J Neurochem. 1994 Mar;62(3):1089-96. doi: 10.1046/j.1471-4159.1994.62031089.x.
The brain, with the exception of the choroid plexuses and circumventricular organs, is partially protected from the invasion of blood-borne chemicals by the specific morphological properties of the cerebral micro-vessels, namely, the tight junctions of the blood-brain barrier. Recently, several enzymes that are primarily involved in hepatic drug metabolism have been shown to exist in the brain, albeit at relatively low specific activities. In the present study, the hypothesis that these enzymes are located primarily at blood-brain interfaces, where they form an "enzymatic barrier," is tested. By using microdissection techniques or a gradient-centrifugation isolation procedure, the activities of seven drug-metabolizing enzymes in isolated microvessels, choroid plexuses, meningeal membranes, and tissue from three circumventricular organs (the neural lobe of the hypophysis, pineal gland, and median eminence) were assayed. With two exceptions, the activities of these enzymes were higher in the three circumventricular organs and cerebral microvessel than in the cortex. Very high membrane-bound epoxide hydrolase and UDP-glucuronosyltransferase activities (approaching those in liver) and somewhat high 7-benzoxyresorufin-O-dealkylase and NADPH-cytochrome P-450 reductase activities were determined in the choroid plexuses. The pia-arachnoid membranes, but not the dura matter, displayed drug-metabolizing enzyme activities, notably that of epoxide hydrolase. The drug-metabolizing enzymes located at these nonparenchymal sites may function to protect brain tissue from harmful compounds.
除脉络丛和室周器官外,大脑通过脑微血管的特定形态学特性(即血脑屏障的紧密连接)部分地免受血源性化学物质的侵入。最近,已证明几种主要参与肝脏药物代谢的酶存在于大脑中,尽管其比活性相对较低。在本研究中,对这些酶主要位于血脑界面并在那里形成“酶屏障”这一假说进行了验证。通过使用显微切割技术或梯度离心分离程序,测定了分离的微血管、脉络丛、脑膜以及三个室周器官(垂体神经叶、松果体和正中隆起)组织中七种药物代谢酶的活性。除两个例外情况外,这些酶在三个室周器官和脑微血管中的活性高于皮质中的活性。在脉络丛中测定到非常高的膜结合环氧化物水解酶和UDP-葡萄糖醛酸基转移酶活性(接近肝脏中的活性)以及较高的7-苯氧基试卤灵-O-脱烷基酶和NADPH-细胞色素P-450还原酶活性。软脑膜-蛛网膜而非硬脑膜显示出药物代谢酶活性,尤其是环氧化物水解酶的活性。位于这些非实质部位的药物代谢酶可能起到保护脑组织免受有害化合物侵害的作用。