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海马内注射秋水仙碱后谷氨酸受体结合位点变化与其与磷脂酰肌醇代谢偶联之间的解离。

Dissociation between changes in glutamate receptor binding sites and their coupling to phosphatidylinositol metabolism following intrahippocampal colchicine injection.

作者信息

Nakagawa Y, Baudry M

机构信息

Center for the Neurobiology of Learning and Memory, University of California, Irvine 92717.

出版信息

Neuroscience. 1989;32(2):363-9. doi: 10.1016/0306-4522(89)90084-5.

Abstract

Intrahippocampal colchicine injection produces a rapid death of granule cells and pyramidal neurons in the hippocampus in the rat. Under the appropriate assay conditions, [3H]glutamate labels the N-methyl-D-aspartate type of glutamate receptors while [3H]alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate labels the quisqualate type. Unilateral injection of colchicine (15 micrograms) in the dorsal hippocampus did not produce any change in [3H]glutamate and [3H]alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate binding in membrane fractions from the dentate gyrus or CA1 field contralateral to the injection side, at least up to 12 days after the injection. However, it produced a progressive decrease in the binding of both ligands in dentate gyrus and CA1 of the injected hippocampus. In the dentate gyrus the changes in binding as a function of time after the injection were biphasic with a rapid exponential decrease (t1/2 about 8 days for both [3H]glutamate and [3H]alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate) until 12 days after the injection followed by a much slower decrease afterwards. A similar pattern was observed in CA1 although the changes in binding were smaller and delayed by about three days as compared to the dentate gyrus. Kinetic analyses of the binding at equilibrium were performed seven days after the injection and indicated that the changes in [3H]glutamate binding were due to a change in the maximum number of sites but not in affinity for the ligand.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

海马体内注射秋水仙碱会导致大鼠海马中的颗粒细胞和锥体神经元迅速死亡。在适当的检测条件下,[3H]谷氨酸标记N-甲基-D-天冬氨酸型谷氨酸受体,而[3H]α-氨基-3-羟基-5-甲基异恶唑-4-丙酸标记quisqualate型受体。在背侧海马单侧注射秋水仙碱(15微克),在注射侧对侧的齿状回或CA1区的膜组分中,[3H]谷氨酸和[3H]α-氨基-3-羟基-5-甲基异恶唑-4-丙酸结合至少在注射后12天内未发生任何变化。然而,它使注射侧海马的齿状回和CA1区中两种配体的结合逐渐减少。在齿状回中,注射后结合随时间的变化呈双相性,快速指数下降([3H]谷氨酸和[3H]α-氨基-3-羟基-5-甲基异恶唑-4-丙酸的t1/2约为8天),直至注射后12天,随后下降速度慢得多。在CA1区观察到类似模式,尽管与齿状回相比,结合变化较小且延迟约三天。注射后七天进行平衡结合的动力学分析,结果表明[3H]谷氨酸结合的变化是由于位点最大数量的改变,而不是对配体亲和力的改变。(摘要截断于250字)

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