Hu Bo, Sun Sheng-Gang, Tong E-Tang
Neurology Department, Union Hospital, Tongji College, Huazhong University of Science and Technology, Wuhan 430022, China.
Acta Pharmacol Sin. 2004 Jun;25(6):714-20.
To study the effect of glutamate on the intracellular calcium signal of pure cultured rat astrocytes and the role of N-methyl-D-aspartate (NMDA) and alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA) receptors in the procedure.
The fluorescence of calcium was measured by Fura-2/AM (F(345)/F(380)).
L-Glutamate induced Ca(2+) increase in most of the cells in concentration- and time-dependent manner. NMDA 50 mmol/L induced the fluorescence increase by almost three to four times, while the effect of AMPA 50 mmol/L was just half of that of D-(-)-2-amino-5-phosphonopentanoic acid (D-AP-5; a selective antagonist of the NMDA receptor). 6-Cyano-7-nitroquinoxaline-2,3-dione (CNQX, a selective antagonist of the AMPA receptor) abolished the effects of NMDA and AMPA, respectively. D-AP-5 and CNQX simultaneously or respectively attenuated the effect of L-glutamate at different degrees, but could not abolish it entirely.
Glutamate modulated intracellular Ca(2+) of pure cultured rat astrocytes through different pathways. The activation of NMDA and AMPA receptors took part in the complex mechanisms.
研究谷氨酸对原代培养大鼠星形胶质细胞内钙信号的影响以及N-甲基-D-天冬氨酸(NMDA)和α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体在此过程中的作用。
采用Fura-2/AM(F(345)/F(380))检测钙荧光。
L-谷氨酸以浓度和时间依赖的方式诱导大多数细胞内[Ca(2+)]升高。50 mmol/L的NMDA诱导荧光增加近三到四倍,而50 mmol/L的AMPA的作用仅为D-(-)-2-氨基-5-膦酰基戊酸(D-AP-5;NMDA受体的选择性拮抗剂)的一半。6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX,AMPA受体的选择性拮抗剂)分别消除了NMDA和AMPA的作用。D-AP-5和CNQX同时或分别不同程度地减弱了L-谷氨酸的作用,但不能完全消除。
谷氨酸通过不同途径调节原代培养大鼠星形胶质细胞内的Ca(2+)。NMDA和AMPA受体的激活参与了这一复杂机制。