Lin T A, Lin T N, He Y Y, Hsu C Y, Sun G Y
Biochemistry Department, University of Missouri-School of Medicine, Columbia 65212.
Biochem Biophys Res Commun. 1992 Apr 30;184(2):871-7. doi: 10.1016/0006-291x(92)90671-7.
Ins(1,4,5)P3 3-kinase and 5-phosphatase are important enzymes responsible for the metabolism of Ins(1,4,5)P3, a second messenger for mobilization of intracellular Ca2+ stores. Focal cerebral ischemia induced in Long Evans rats through occlusion of the right middle cerebral artery (MCA) and both common carotid arteries resulted in a time-dependent decrease in the 3-kinase activity but not the 5-phosphatase activity. Approximately 50% of the 3-kinase activity in the cerebral cortex of the right MCA territory disappeared after 60 min of ischemia, and the enzyme activity was not restored during reperfusion. Reperfusion for 24 hr after a 60 min ischemic insult almost abolished the 3-kinase activity but the 5-phosphatase activity remained unaltered. These results suggest that the Ins(1,4,5)P3 3-kinase is one of the target enzymes of cerebral ischemia. The changes in Ins(1,4,5)P3 metabolism may be associated with the changes in intracellular Ca2+ homeostasis that underlies the pathophysiology of neuronal cell death.
肌醇-1,4,5-三磷酸(Ins(1,4,5)P3)3-激酶和5-磷酸酶是负责Ins(1,4,5)P3代谢的重要酶,Ins(1,4,5)P3是动员细胞内钙库的第二信使。通过闭塞右大脑中动脉(MCA)和双侧颈总动脉在Long Evans大鼠中诱导局灶性脑缺血,导致3-激酶活性呈时间依赖性下降,但5-磷酸酶活性未下降。缺血60分钟后,右侧MCA区域大脑皮质中约50%的3-激酶活性消失,且在再灌注期间酶活性未恢复。60分钟缺血性损伤后再灌注24小时几乎消除了3-激酶活性,但5-磷酸酶活性保持不变。这些结果表明,Ins(1,4,5)P3 3-激酶是脑缺血的靶酶之一。Ins(1,4,5)P3代谢的变化可能与细胞内钙稳态的变化有关,而细胞内钙稳态是神经元细胞死亡病理生理学的基础。