Retz K C, Coyle J T
Neuropharmacology. 1984 Jan;23(1):89-94. doi: 10.1016/0028-3908(84)90222-3.
Exposure to L-glutamate (10 mM) or 60 mM K+ for 1 min significantly stimulated the uptake of 45Ca2+ in slices from mouse striatum. Glutamate-induced stimulation was antagonized by 30 mM Mg2+ and by 5 or 10 mM L-glutamic acid diethyl ester, but not by 5 microM tetrodotoxin. Under these 1-min incubation conditions, neither kainate nor N-methyl-D,L-aspartate significantly affected the uptake of 45Ca2+ ion. By contrast, following preincubation for 10 min, glutamate and the conformationally restricted analogues, ibotenate, quisqualate, and kainate significantly inhibited the 60 mM K+-induced stimulation of the uptake of 45Ca2+. These effects of glutamate and kainate were not significantly affected by the presence of 1 mM Ca2+ in the preincubation medium. These results suggest that glutamate may activate a receptor directly linked to Ca2+ channels, whereas kainate may indirectly modulate the intracellular disposition of Ca2+.
将小鼠纹状体切片暴露于10 mM的L-谷氨酸或60 mM的K⁺中1分钟,可显著刺激⁴⁵Ca²⁺的摄取。谷氨酸诱导的刺激作用被30 mM的Mg²⁺以及5或10 mM的L-谷氨酸二乙酯拮抗,但不被5 μM的河豚毒素拮抗。在这些1分钟的孵育条件下,海人酸和N-甲基-D,L-天冬氨酸均未显著影响⁴⁵Ca²⁺离子的摄取。相比之下,在预孵育10分钟后,谷氨酸及其构象受限类似物鹅膏蕈氨酸、quisqualate和海人酸显著抑制了60 mM K⁺诱导的⁴⁵Ca²⁺摄取刺激。预孵育培养基中存在1 mM Ca²⁺对谷氨酸和海人酸的这些作用没有显著影响。这些结果表明,谷氨酸可能激活直接与Ca²⁺通道相连的受体,而海人酸可能间接调节细胞内Ca²⁺的分布。