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电生理学鉴定大鼠视上核单个血管加压素神经元上的功能性突触前神经末梢。

Electrophysiological identification of the functional presynaptic nerve terminals on an isolated single vasopressin neurone of the rat supraoptic nucleus.

机构信息

Department of Physiology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan.

出版信息

J Neuroendocrinol. 2010 May;22(5):413-9. doi: 10.1111/j.1365-2826.2010.01979.x. Epub 2010 Feb 12.

DOI:10.1111/j.1365-2826.2010.01979.x
PMID:20163519
Abstract

Release of arginine vasopressin (AVP) and oxytocin from magnocellular neurosecretory cells (MNCs) of the supraoptic nucleus (SON) is under the control of glutamate-dependent excitation and GABA-dependent inhibition. The possible role of the synaptic terminals attached to SON neurones has been investigated using whole-cell patch-clamp recording in in vitro rat brain slice preparations. Recent evidence has provided new insights into the repercussions of glial environment modifications on the physiology of MNCs at the synaptic level in the SON. In the present study, excitatory glutamatergic and inhibitory GABAergic synaptic inputs were recorded from an isolated single SON neurone cultured for 12 h, using the whole-cell patch clamp technique. Neurones expressed an AVP-enhanced green fluorescent protein (eGFP) fusion gene in MNCs. In addition, native synaptic terminals attached to a dissociated AVP-eGFP neurone were visualised with synaptic vesicle markers. These results suggest that the function of presynaptic nerve terminals may be evaluated directly in a single AVP-eGFP neurone. These preparations would be helpful in future studies aiming to electrophysiologically distinguish between the functions of synaptic terminals and glial modifications in the SON neurones.

摘要

精氨酸加压素(AVP)和催产素从视上核(SON)的大细胞神经分泌细胞(MNC)释放受谷氨酸能兴奋和 GABA 能抑制的控制。使用体外大鼠脑片制备中的全细胞膜片钳记录研究了附着于 SON 神经元的突触末梢的可能作用。最近的证据提供了新的见解,即神经胶质环境改变对 SON 中突触水平上 MNC 生理学的影响。在本研究中,使用全细胞膜片钳技术从培养 12 小时的单个分离的 SON 神经元中记录了兴奋性谷氨酸能和抑制性 GABA 能突触输入。神经元在 MNC 中表达 AVP 增强型绿色荧光蛋白(eGFP)融合基因。此外,用突触小泡标记物可视化了附着在分离的 AVP-eGFP 神经元上的天然突触末梢。这些结果表明,可以直接在单个 AVP-eGFP 神经元中评估突触前神经末梢的功能。这些制剂将有助于未来的研究,旨在电生理上区分 SON 神经元中突触末梢和神经胶质改变的功能。

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