• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

大鼠小脑神经元中L型钙通道的功能多样性

Functional diversity of L-type calcium channels in rat cerebellar neurons.

作者信息

Forti L, Pietrobon D

机构信息

Department of Biomedical Sciences, C.N.R. Center of Physiology and Mitochondria, University of Padova, Italy.

出版信息

Neuron. 1993 Mar;10(3):437-50. doi: 10.1016/0896-6273(93)90332-l.

DOI:10.1016/0896-6273(93)90332-l
PMID:8384858
Abstract

Single-channel recordings show that functionally different L-type Ca2+ channels coexist in rat cerebellar granules. Besides two different dihydropyridine (DHP)-sensitive gating patterns with properties similar to those of cardiac L-type channels, cerebellar granules contain a third DHP-sensitive gating pattern with unusual voltage-dependent properties and slightly different conductance. This "anomalous gating" is characterized, on one hand, by rare, short openings with very low open probability even at high positive voltages and, on the other hand, by long openings with high open probability at negative voltages after a predepolarization. L-type channels with anomalous gating appear suited to generate a surge of Ca2+ influx following strong neuronal activity. The anomalous gating can be explained by a model in which voltage controls the equilibrium between two gating modes.

摘要

单通道记录表明,功能不同的L型Ca2+通道共存于大鼠小脑颗粒细胞中。除了两种不同的对二氢吡啶(DHP)敏感的门控模式,其特性与心脏L型通道相似外,小脑颗粒细胞还包含第三种对DHP敏感的门控模式,具有不寻常的电压依赖性特性和略有不同的电导。这种“异常门控”一方面表现为即使在高正电压下也很少有短暂开放且开放概率极低,另一方面表现为在预去极化后负电压下有高开放概率的长时开放。具有异常门控的L型通道似乎适合在强烈神经元活动后产生Ca2+内流激增。异常门控可以用一个电压控制两种门控模式之间平衡的模型来解释。

相似文献

1
Functional diversity of L-type calcium channels in rat cerebellar neurons.大鼠小脑神经元中L型钙通道的功能多样性
Neuron. 1993 Mar;10(3):437-50. doi: 10.1016/0896-6273(93)90332-l.
2
Ethanol directly modulates gating of a dihydropyridine-sensitive Ca2+ channel in neurohypophysial terminals.乙醇直接调节神经垂体终末中对二氢吡啶敏感的Ca2+通道的门控。
J Neurosci. 1994 Sep;14(9):5453-60. doi: 10.1523/JNEUROSCI.14-09-05453.1994.
3
Selective potentiation of a novel calcium channel in rat hippocampal neurones.大鼠海马神经元中一种新型钙通道的选择性增强作用。
J Physiol. 1994 Nov 1;480 ( Pt 3)(Pt 3):475-84. doi: 10.1113/jphysiol.1994.sp020376.
4
Fast activation of dihydropyridine-sensitive calcium channels of skeletal muscle. Multiple pathways of channel gating.骨骼肌中二氢吡啶敏感钙通道的快速激活。通道门控的多种途径。
J Gen Physiol. 1996 Sep;108(3):221-32. doi: 10.1085/jgp.108.3.221.
5
Three novel types of voltage-dependent calcium channels in rat cerebellar neurons.大鼠小脑神经元中三种新型电压依赖性钙通道。
J Neurosci. 1994 Sep;14(9):5243-56. doi: 10.1523/JNEUROSCI.14-09-05243.1994.
6
Nonmodal gating of cardiac calcium channels as revealed by dihydropyridines.二氢吡啶揭示的心脏钙通道非模式门控
J Gen Physiol. 1989 Jun;93(6):1243-73. doi: 10.1085/jgp.93.6.1243.
7
Novel mechanism of voltage-dependent gating in L-type calcium channels.L型钙通道中电压依赖性门控的新机制。
Nature. 1990 Aug 16;346(6285):651-5. doi: 10.1038/346651a0.
8
Anomalous L-type calcium channels of rat spinal motoneurons.大鼠脊髓运动神经元的异常L型钙通道。
J Gen Physiol. 1999 May;113(5):679-94. doi: 10.1085/jgp.113.5.679.
9
Inactivating and non-inactivating dihydropyridine-sensitive Ca2+ channels in mouse cerebellar granule cells.小鼠小脑颗粒细胞中失活和非失活的二氢吡啶敏感性Ca2+通道
J Physiol. 1991 Aug;439:301-23. doi: 10.1113/jphysiol.1991.sp018668.
10
Characteristics of calcium channels responsible for voltage-activated calcium entry in rat cerebellar granule cells.负责大鼠小脑颗粒细胞中电压激活钙内流的钙通道特性。
Eur J Neurosci. 1994 Mar 1;6(3):335-44. doi: 10.1111/j.1460-9568.1994.tb00276.x.

引用本文的文献

1
The Molecular Basis for the Calcium-Dependent Slow Afterhyperpolarization in CA1 Hippocampal Pyramidal Neurons.CA1海马锥体神经元中钙依赖性慢后超极化的分子基础。
Front Physiol. 2021 Dec 22;12:759707. doi: 10.3389/fphys.2021.759707. eCollection 2021.
2
Voltage-Gated Ca-Channel α1-Subunit Missense Mutations: Gain or Loss of Function - Implications for Potential Therapies.电压门控钙通道α1亚基错义突变:功能获得或丧失——对潜在治疗的影响
Front Synaptic Neurosci. 2021 Mar 3;13:634760. doi: 10.3389/fnsyn.2021.634760. eCollection 2021.
3
Neuritin promotes neurite and spine growth in rat cerebellar granule cells via L-type calcium channel-mediated calcium influx.
神经黏附素通过 L 型钙通道介导的钙内流促进大鼠小脑颗粒细胞的突起和棘突生长。
J Neurochem. 2018 Oct;147(1):40-57. doi: 10.1111/jnc.14535. Epub 2018 Aug 16.
4
GDF-15 enhances intracellular Ca2+ by increasing Cav1.3 expression in rat cerebellar granule neurons.生长分化因子15(GDF-15)通过增加大鼠小脑颗粒神经元中Cav1.3的表达来增强细胞内钙离子浓度。
Biochem J. 2016 Jul 1;473(13):1895-904. doi: 10.1042/BCJ20160362. Epub 2016 Apr 25.
5
Small-conductance Ca2+-activated K+ channels modulate action potential-induced Ca2+ transients in hippocampal neurons.小电导钙激活钾通道调节海马神经元动作电位诱导的钙瞬变。
J Neurophysiol. 2013 Mar;109(6):1514-24. doi: 10.1152/jn.00346.2012. Epub 2012 Dec 19.
6
Interleukin-6 inhibits L-type calcium channel activity of cultured cerebellar granule neurons.白细胞介素-6 抑制培养的小脑颗粒神经元 L 型钙通道活性。
J Physiol Sci. 2012 Sep;62(5):385-92. doi: 10.1007/s12576-012-0215-x. Epub 2012 Jun 14.
7
Domain III regulates N-type (CaV2.2) calcium channel closing kinetics.结构域 III 调节 N 型(钙通道 2.2)钙通道关闭动力学。
J Neurophysiol. 2012 Apr;107(7):1942-51. doi: 10.1152/jn.00993.2011. Epub 2011 Dec 28.
8
Molecular nature of anomalous L-type calcium channels in mouse cerebellar granule cells.小鼠小脑颗粒细胞中异常L型钙通道的分子特性
J Neurosci. 2007 Apr 4;27(14):3855-63. doi: 10.1523/JNEUROSCI.4028-06.2007.
9
Gating of the HypoPP-1 mutations: I. Mutant-specific effects and cooperativity.低钾型周期性麻痹-1突变的门控:I. 突变特异性效应与协同性
Pflugers Arch. 2007 Jun;454(3):495-505. doi: 10.1007/s00424-007-0225-3. Epub 2007 Feb 27.
10
Erbin enhances voltage-dependent facilitation of Ca(v)1.3 Ca2+ channels through relief of an autoinhibitory domain in the Ca(v)1.3 alpha1 subunit.Erbin通过解除Ca(v)1.3 α1亚基中的自身抑制结构域来增强Ca(v)1.3钙通道的电压依赖性易化作用。
J Neurosci. 2007 Feb 7;27(6):1374-85. doi: 10.1523/JNEUROSCI.5191-06.2007.