Lindström P, Ohlsson L
Department of Histology and Cell Biology, University of Umeå, Sweden.
Endocrinology. 1992 Oct;131(4):1903-7. doi: 10.1210/endo.131.4.1396334.
The effect of excitatory amino acid receptor agonists on GH secretion was tested in isolated male rat somatotrophs. N-Methyl-D,L-Aspartate (NMDA) had a dose-dependent stimulatory effect on GH secretion in perifused somatotrophs. The effect was observed already during the first minute after exposure to NMDA and was reversible after its omission. The effect of 1 microM NMDA was inhibited by the NMDA receptor antagonists 10 microM AP7 and 5 microM MK801, and by 5 microM dextromethorphan. L-Glutamate, 100 microM, and 100 microM kainic acid also stimulated GH secretion. The stimulatory effect of NMDA on GH release was paralleled by an increase in 45Ca efflux and an increase in somatotroph intracellular calcium concentration. Efflux of 86Rb (tracer for potassium) was not affected by NMDA. It is concluded that excitatory amino acids can stimulate GH secretion in rats through a direct effect on the somatotrophs.
在分离的雄性大鼠生长激素细胞中测试了兴奋性氨基酸受体激动剂对生长激素分泌的影响。N-甲基-D,L-天冬氨酸(NMDA)对灌流的生长激素细胞的生长激素分泌具有剂量依赖性刺激作用。在暴露于NMDA后的第一分钟内就观察到了这种作用,在去除NMDA后该作用是可逆的。1 microM NMDA的作用被NMDA受体拮抗剂10 microM AP7、5 microM MK801和5 microM右美沙芬抑制。100 microM的L-谷氨酸和100 microM的 kainic 酸也刺激生长激素分泌。NMDA对生长激素释放的刺激作用与45Ca外流增加和生长激素细胞内钙浓度增加平行。86Rb(钾的示踪剂)的外流不受NMDA影响。得出的结论是,兴奋性氨基酸可通过对生长激素细胞的直接作用来刺激大鼠的生长激素分泌。