论文部分内容阅读
为探讨胆囊收缩素八肽(cholecystokinin octapeptide, CCK-8)及中毒剂量谷氨酸(glutamate, Glu)对大鼠大脑皮质细胞内Ca2+浓度([Ca2+]i)的影响及相互关系,以10-10、 10-8、 10-6mol/L等浓度CCK-8和1mmol/L Glu分别或共同作用于大鼠大脑皮质驯胞,以流式细胞仪( Flow cytometer, FCM)检测[Ca2+]i,并探讨其变化机制。① 10-10 mol/LCCK-8可增加[Ca2+]i(P<0.05), 10-8、10-6mol/LCCK-8无此作用;②10-10mol/LCCK-8与1mmol/L Glu共同作用可增加[Ca2+]i(P<0.05),而10-6mo1/LCCK-8不引起[Ca2+]i增加;③当抑制细胞内钙库释放时,10-10mol/LCCK-8加1mmolL Glu不能增加[Ca2+]i。结果提示CCK-8生理浓度时可增加[Ca2+]i,而高浓度时无此作用;CCK-8在增加[Ca2+]i的同时有拮抗 Glu引起的细胞外钙内流作用。
To investigate the effect of cholecystokinin octapeptide (CCK-8) and glutamate (Glu) on the intracellular Ca2 + concentration ([Ca2 +] i) in rat cerebral cortex, The concentrations of CCK-8, 10 mmol / L, 10-6 mol·L-1 and 1 mmol / L Glu, respectively, were applied to rat cerebral cortex and detected by flow cytometer (FCM) And explore its mechanism of change. ①10-10mol / L CCK-8 could increase [Ca2 +] i (P <0.05), while10-8mol / L CCK-810-8mol / L (P <0.05), while 10-6mo1 / LCCK-8 did not cause [Ca2 +] i increase; ③ When inhibiting intracellular calcium release, 10-10mol / L CCK-8 plus 1 mmol L Glu does not increase [Ca 2+] i. The results suggested that [Ca2 +] i increased at the concentration of CCK-8, but no effect at high concentration. CCK-8 could antagonize Glu-induced extracellular calcium influx while increasing [Ca2 +] i.