Halpain S, McEwen B S
Laboratory of Neuroendocrinology, Rockefeller University, New York, N.Y.
Neuroendocrinology. 1988 Sep;48(3):235-41. doi: 10.1159/000125017.
The effect of in vivo corticosterone manipulation on binding sites for the excitatory neurotransmitter glutamate was determined using radioligand binding to rat brain cryostat sections and crude synaptic membranes. 3H-glutamate binding to regions of the dorsal hippocampal formation was significantly decreased in adrenalectomized animals following 5-10 days of corticosterone treatment. Corticosterone did not alter 3H-glutamate binding in several other brain regions. The loss in 3H-glutamate binding appeared to be due to a decrease in the maximal number of binding sites, with little change in binding affinity. Both chloride-dependent and chloride-independent 3H-glutamate binding sites were decreased by corticosterone treatment. results indicate that corticosterone can selectively alter binding sites for excitatory amino acids in hippocampal tissue.
利用放射性配体与大鼠脑低温切片和粗制突触膜的结合,确定了体内皮质酮操纵对兴奋性神经递质谷氨酸结合位点的影响。在肾上腺切除的动物中,给予皮质酮处理5 - 10天后,3H - 谷氨酸与背侧海马结构区域的结合显著减少。皮质酮对其他几个脑区的3H - 谷氨酸结合没有影响。3H - 谷氨酸结合的减少似乎是由于结合位点的最大数量减少,而结合亲和力变化不大。皮质酮处理使依赖氯化物和不依赖氯化物的3H - 谷氨酸结合位点均减少。结果表明,皮质酮可选择性地改变海马组织中兴奋性氨基酸的结合位点。