Kinuta Y, Kimura M, Itokawa Y, Ishikawa M, Kikuchi H
Department of Neurosurgery, Faculty of Medicine, Kyoto University, Japan.
J Neurosurg. 1989 Sep;71(3):417-20. doi: 10.3171/jns.1989.71.3.0417.
Xanthine oxidase activity in the rat brain was measured by means of high-performance liquid chromatography with electrochemical detection of uric acid. Cerebral ischemia was produced by a four-vessel occlusion method. In the control rat, the enzyme activity was 0.87 +/- 0.13 nmol/gm wet weight/min at 25 degrees C (mean +/- standard deviation), of which 92.4% was associated with the nicotinamide adenine dinucleotide (NAD)-dependent dehydrogenase form and only 7.6% with the oxygen-dependent superoxide-producing oxidase form. However, the ratio of the latter form increased to 43.7% after 30 minutes of global ischemia, despite the total xanthine oxidase activity remaining the same. Thus, it was revealed that uric acid can be synthesized in the rat brain and that cerebral ischemia induced the conversion of xanthine oxidase from an NAD-dependent dehydrogenase to an oxygen-dependent superoxide-producing oxidase. Although the xanthine oxidase pathway has been proposed as a source of oxygen-derived free radicals in various ischemic organs other than brain, the results of the present study suggest the involvement of the oxygen free radicals generated from this pathway in the pathogenesis of the ischemic injury of the rat brain.
采用高效液相色谱法并通过对尿酸进行电化学检测来测定大鼠脑内的黄嘌呤氧化酶活性。通过四血管闭塞法制造脑缺血模型。在对照大鼠中,25℃时该酶活性为0.87±0.13 nmol/g湿重/分钟(平均值±标准差),其中92.4%与烟酰胺腺嘌呤二核苷酸(NAD)依赖性脱氢酶形式相关,仅有7.6%与氧依赖性超氧化物生成氧化酶形式相关。然而,尽管总黄嘌呤氧化酶活性保持不变,但全脑缺血30分钟后,后一种形式的比例增加到了43.7%。由此可见,尿酸可在大鼠脑内合成,且脑缺血促使黄嘌呤氧化酶从NAD依赖性脱氢酶转变为氧依赖性超氧化物生成氧化酶。尽管黄嘌呤氧化酶途径已被认为是除脑之外的各种缺血器官中氧衍生自由基的一个来源,但本研究结果提示该途径产生的氧自由基参与了大鼠脑缺血损伤的发病机制。