Iijima S, Hara K, Suga H, Nakamura S, Kameyama M
Stroke. 1986 May-Jun;17(3):529-33. doi: 10.1161/01.str.17.3.529.
Hydroxylase cofactor, monoamine neurotransmitters and their metabolites were measured in ischemic rat brain produced by four-vessel occlusion for 30 and 60 min periods. Slight reduction of hydroxylase cofactor activity was observed in the ischemic cortex after 60 min. Dopamine increased in the brainstem, and its metabolites, 3,4-dihydroxyphenylacetic acid and homovanillic acid, increased throughout the brain. Decrease in norepinephrine was observed in the whole brain. Decrease in serotonin and increase in 5-hydroxyindoleacetic acid, a metabolite of serotonin, was observed in the ischemic cerebral cortex. The present study has revealed that there appears to be no significant relationship between hydroxylase cofactor activity and monoamine levels in the ischemic brain. Thus, the hydroxylase cofactor does not play a main role in regulating monoamine synthesis in the acute phase of brain ischemia.
采用四动脉闭塞法分别造成大鼠脑缺血30分钟和60分钟,检测缺血大鼠脑内羟化酶辅因子、单胺类神经递质及其代谢产物。60分钟后,缺血皮层的羟化酶辅因子活性略有降低。脑干中的多巴胺增加,其代谢产物3,4 -二羟基苯乙酸和高香草酸在全脑均增加。全脑去甲肾上腺素减少。在缺血性大脑皮层中观察到血清素减少,血清素的代谢产物5 -羟吲哚乙酸增加。本研究表明,在缺血性脑内,羟化酶辅因子活性与单胺水平之间似乎没有显著关系。因此,在脑缺血急性期,羟化酶辅因子在调节单胺合成中不发挥主要作用。