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大鼠海马神经元中非选择性阳离子通道的聚阳离子钙敏感受体激动剂调节作用

Modulation by polycationic Ca(2+)-sensing receptor agonists of nonselective cation channels in rat hippocampal neurons.

作者信息

Ye C, Kanazirska M, Quinn S, Brown E M, Vassilev P M

机构信息

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.

出版信息

Biochem Biophys Res Commun. 1996 Jul 5;224(1):271-80. doi: 10.1006/bbrc.1996.1019.

Abstract

We recently cloned an extracellular calcium (Ca2+0)-sensing receptor (CaR) from bovine parathyroid. The CaR is also expressed in various regions of brain, suggesting that it could potentially mediate some of the well-known but poorly understood effects of Ca2+0 on neuronal function. We have now examined the effects of polycationic CaR agonists on the activity of nonselective cation channels (NCC) in cultured rat hippocampal neurons, using the cell-attached configuration of the patch clamp technique and applying CaR active agents to the external bath solution. The polycationic CaR agonist, neomycin (100 microM), as well as an elevated concentration of Ca2+0 (3 mM), which is known to activate the cloned CaR, significantly increased the probability of channel opening (Po). The polyamine, spermine (300 microM), which also mimics the actions of Ca2+0 on the cloned CaR, produced similar changes in Po in rat hippocampal neurons. Elevation of Ca2+0 also increased Po for a similar NCC in HEK293 cells transfected with the cloned human CaR but not in nontransfected HEK cells. Thus the CaR can regulate the activity of Ca(2+)-permeable NCC in hippocampal neurons and could potentially modulate key functions of these cells, including neurotransmission and neuronal excitability.

摘要

我们最近从牛甲状旁腺中克隆出一种细胞外钙(Ca2+0)传感受体(CaR)。CaR也在大脑的各个区域表达,这表明它可能介导了Ca2+0对神经元功能的一些众所周知但了解甚少的作用。我们现在使用膜片钳技术的细胞贴附式记录模式,并将CaR激动剂应用于细胞外浴液,研究了多阳离子CaR激动剂对培养的大鼠海马神经元中非选择性阳离子通道(NCC)活性的影响。多阳离子CaR激动剂新霉素(100微摩尔),以及已知能激活克隆的CaR的升高浓度的Ca2+0(3毫摩尔),显著增加了通道开放的概率(Po)。多胺精胺(300微摩尔),它也模拟Ca2+0对克隆的CaR的作用,在大鼠海马神经元中使Po产生了类似的变化。Ca2+0的升高也增加了转染了克隆的人CaR的HEK293细胞中类似NCC的Po,但在未转染的HEK细胞中没有增加。因此,CaR可以调节海马神经元中Ca(2+)通透性NCC的活性,并可能潜在地调节这些细胞的关键功能,包括神经传递和神经元兴奋性。

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