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二价阳离子对豚鼠小肠平滑肌毒蕈碱受体阳离子电流的影响。

Effects of divalent cations on muscarinic receptor cationic current in smooth muscle from guinea-pig small intestine.

作者信息

Zholos A V, Bolton T B

机构信息

Department of Pharmacology and Clinical Pharmacology, St George's Hospital Medical School, London, UK.

出版信息

J Physiol. 1995 Jul 1;486 ( Pt 1)(Pt 1):67-82. doi: 10.1113/jphysiol.1995.sp020791.

Abstract
  1. Effects of Mg2+ and Ca2+ on muscarinic receptor cationic current (Icat) in guinea-pig ileal smooth muscle cells have been studied using patch-clamp techniques (whole-cell recording). Icat was activated either by externally applied carbachol or, to bypass receptors, by intracellular GTP-gamma-S. 2. Independently of the main permeant cation the current-voltage (I-V) relation for Icat was U-shaped between the reversal potential (usually 0 mV) and very negative potentials such as -120 mV where current could be virtually lost. Adding Ca2+ to Ca(2+)- and Mg(2+)-free external solution reduced inward current and made it less U-shaped whereas adding Mg2+ reduced inward current and shifted more positively the potential at which maximum inward current occurred. 3. Activation of the conductance underlying Icat could be described by the Boltzmann relation which was shifted positively by adding Ca2+ or Mg2+. Extracellular Ca2+ also distorted the relation by increasing the slope factor; maximal conductance was reduced in all cases. Icat relaxation at negative potentials was accelerated by increasing Mg2+ and slowed down by Ca2+. 4. These data suggest the presence of fixed negative surface charges on or near the muscarinic receptor cationic channel, which allow its modulation through alteration of surface potential. Additional more direct ion binding to and blocking of the channel cannot be ruled out. Some additional effects of Ca2+ (if compared with Mg2+) could be explained on the assumption that the Ca(2+)-binding activation site known to be present on the internal side of the channel can be accessible to Ca2+ entering through the open channel during muscarinic receptor stimulation, as Ca2+ ions contribute to a limited extent to Icat. 5. We conclude that voltage-dependent gating of muscarinic receptor cationic channels is an intrinsic channel property and that Ca2+ and Mg2+ have strong modulatory effects.
摘要
  1. 运用膜片钳技术(全细胞记录)研究了Mg2+和Ca2+对豚鼠回肠平滑肌细胞毒蕈碱受体阳离子电流(Icat)的影响。Icat可通过细胞外施加卡巴胆碱激活,或者为绕过受体,通过细胞内GTP-γ-S激活。2. 与主要通透阳离子无关,Icat的电流-电压(I-V)关系在反转电位(通常为0 mV)和非常负的电位(如-120 mV,此时电流实际上可能消失)之间呈U形。向无Ca2+和Mg2+的细胞外溶液中添加Ca2+会降低内向电流并使其U形减弱,而添加Mg2+会降低内向电流并使最大内向电流出现时的电位更正向移动。3. Icat所依赖的电导激活可用玻尔兹曼关系描述,添加Ca2+或Mg2+会使其正向移动。细胞外Ca2+还会通过增加斜率因子使该关系变形;所有情况下最大电导均降低。负电位下Icat的松弛通过增加Mg2+而加速,通过Ca2+而减慢。4. 这些数据表明在毒蕈碱受体阳离子通道上或其附近存在固定的负表面电荷,这允许通过改变表面电位对其进行调节。不能排除离子与通道的额外更直接结合和阻断。Ca2+(与Mg2+相比)的一些额外作用可以基于这样的假设来解释,即已知存在于通道内侧的Ca2+结合激活位点在毒蕈碱受体刺激期间可被通过开放通道进入的Ca2+所接近,因为Ca2+离子对Icat的贡献有限。5. 我们得出结论,毒蕈碱受体阳离子通道的电压依赖性门控是一种内在的通道特性,并且Ca2+和Mg2+具有很强的调节作用。

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