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大鼠小脑颗粒细胞与浦肯野细胞在解离细胞培养中的突触传递:兴奋性氨基酸递质拮抗剂的作用

Synaptic transmission between rat cerebellar granule and Purkinje cells in dissociated cell culture: effects of excitatory-amino acid transmitter antagonists.

作者信息

Hirano T, Hagiwara S

机构信息

Department of Physiology, Jerry Lewis Neuromuscular Research Center, Los Angeles, CA.

出版信息

Proc Natl Acad Sci U S A. 1988 Feb;85(3):934-8. doi: 10.1073/pnas.85.3.934.

Abstract

Monosynaptic excitatory connections between cerebellar granule and Purkinje cells were studied in dissociated cell cultures, and identification of the transmitter and the postsynaptic receptor at this synapse was pharmacologically investigated. The presynaptic granule cell and the postsynaptic Purkinje cell were voltage- or current-clamped simultaneously, and the excitatory postsynaptic current induced by the granule cell was examined. The neurons and monosynaptic excitatory connections were identified as in our earlier study. Several pairs of granule and Purkinje cells were stained with Lucifer yellow and propidium iodide, respectively, and their morphology was examined after electrophysiological recording. The monosynaptic excitatory postsynaptic current was suppressed by 1 mM kynurenate, an antagonist for excitatory-amino acid receptors, but was little affected by 0.2 mM DL-2-amino-5-phosphonovalerate, a selective antagonist of N-methyl-D-aspartate receptors. Glutamate and aspartate induced inward current in the Purkinje cells. These currents were suppressed by kynurenate at 1 mM. DL-2-Amino-5-phosphonovalerate at 0.2 mM suppressed the inward current induced by 100 microM aspartate but did not affect the inward current induced by 10 microM glutamate. These results are consistent with the idea that glutamate, or a glutamate-like substance, but not aspartate is the transmitter released at the synapse between granule and Purkinje cells and that non-N-methyl-D-aspartate receptor channels are functioning in the postsynaptic membrane.

摘要

在解离细胞培养物中研究了小脑颗粒细胞与浦肯野细胞之间的单突触兴奋性连接,并通过药理学方法研究了该突触处的递质和突触后受体。同时对突触前颗粒细胞和突触后浦肯野细胞进行电压钳或电流钳制,并检测颗粒细胞诱导的兴奋性突触后电流。如我们早期研究那样鉴定神经元和单突触兴奋性连接。分别用荧光黄和碘化丙啶对几对颗粒细胞和浦肯野细胞进行染色,并在电生理记录后检查它们的形态。1 mM犬尿氨酸(一种兴奋性氨基酸受体拮抗剂)可抑制单突触兴奋性突触后电流,但0.2 mM DL-2-氨基-5-磷酸戊酸(一种N-甲基-D-天冬氨酸受体的选择性拮抗剂)对其影响很小。谷氨酸和天冬氨酸可在浦肯野细胞中诱导内向电流。这些电流可被1 mM犬尿氨酸抑制。0.2 mM DL-2-氨基-5-磷酸戊酸可抑制由100 μM天冬氨酸诱导的内向电流,但不影响由10 μM谷氨酸诱导的内向电流。这些结果与以下观点一致:谷氨酸或类似谷氨酸的物质而非天冬氨酸是颗粒细胞与浦肯野细胞之间突触处释放的递质,并且非N-甲基-D-天冬氨酸受体通道在突触后膜中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5169/279671/6c8b190190a7/pnas00255-0302-a.jpg

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