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Dual effects of intracellular magnesium on muscarinic potassium channel current in single guinea-pig atrial cells.细胞内镁对豚鼠单个心房肌细胞毒蕈碱钾通道电流的双重作用。
J Physiol. 1989 Jan;408:313-32. doi: 10.1113/jphysiol.1989.sp017461.
2
Rectification of muscarinic K+ current by magnesium ion in guinea pig atrial cells.镁离子对豚鼠心房肌细胞毒蕈碱型钾电流的整流作用
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3
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Effects of external and internal K+ ions on magnesium block of inwardly rectifying K+ channels in guinea-pig heart cells.细胞外和细胞内钾离子对豚鼠心脏细胞内向整流钾通道镁离子阻滞的影响。
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Open-state substructure of inwardly rectifying potassium channels revealed by magnesium block in guinea-pig heart cells.豚鼠心脏细胞中镁离子阻滞揭示内向整流钾通道的开放态亚结构
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Phosphatase is responsible for run down, and probably G protein-mediated inhibition of inwardly rectifying K+ currents in guinea pig chromaffin cells.磷酸酶负责衰减,并且可能在豚鼠嗜铬细胞中通过G蛋白介导抑制内向整流钾电流。
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Role of intracellular Mg2+ in the activation of muscarinic K+ channel in cardiac atrial cell membrane.细胞内镁离子在心房肌细胞膜毒蕈碱钾通道激活中的作用
Pflugers Arch. 1986 Nov;407(5):572-4. doi: 10.1007/BF00657521.

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Acetylcholine-mediated K+ channel activity in guinea-pig atrial cells is supported by nucleoside diphosphate kinase.豚鼠心房细胞中乙酰胆碱介导的钾离子通道活性由核苷二磷酸激酶支持。
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10
Voltage-dependent block by internal Ca2+ ions of inwardly rectifying K+ channels in guinea-pig ventricular cells.豚鼠心室肌细胞内向整流钾通道的内向钙离子电压依赖性阻滞作用
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本文引用的文献

1
Vagal and sympathetic effects on the pacemaker fibers in the sinus venosus of the heart.迷走神经和交感神经对心脏静脉窦起搏纤维的影响。
J Gen Physiol. 1956 May 20;39(5):715-33. doi: 10.1085/jgp.39.5.715.
2
Neutral carrier ion-selective microelectrodes for measurement of intracellular free calcium.用于测量细胞内游离钙的中性载体离子选择性微电极。
Biochim Biophys Acta. 1980 Jul;599(2):623-38. doi: 10.1016/0005-2736(80)90205-9.
3
Calcium tolerant ventricular myocytes prepared by preincubation in a "KB medium".通过在“KB培养基”中预孵育制备的耐钙心室肌细胞。
Pflugers Arch. 1982 Oct;395(1):6-18. doi: 10.1007/BF00584963.
4
Phosphorus nuclear magnetic resonance spectroscopy of cardiac and skeletal muscles.心脏和骨骼肌的磷核磁共振波谱分析
Am J Physiol. 1982 May;242(5):H729-44. doi: 10.1152/ajpheart.1982.242.5.H729.
5
Free magnesium in sheep, ferret and frog striated muscle at rest measured with ion-selective micro-electrodes.用离子选择性微电极测量绵羊、雪貂和青蛙横纹肌静息时的游离镁。
J Physiol. 1982 Dec;333:173-88. doi: 10.1113/jphysiol.1982.sp014447.
6
The A protomer of islet-activating protein, pertussis toxin, as an active peptide catalyzing ADP-ribosylation of a membrane protein.胰岛激活蛋白百日咳毒素的A亚基,作为一种催化膜蛋白ADP核糖基化的活性肽。
Arch Biochem Biophys. 1983 Jul 1;224(1):290-8. doi: 10.1016/0003-9861(83)90212-6.
7
Effects of acetylcholine on electrophysiological properties of rabbit cardiac Purkinje fibers.乙酰胆碱对兔心脏浦肯野纤维电生理特性的影响。
Circ Res. 1983 Dec;53(6):740-51. doi: 10.1161/01.res.53.6.740.
8
NMR studies of intracellular metal ions in intact cells and tissues.完整细胞和组织中细胞内金属离子的核磁共振研究。
Annu Rev Biophys Bioeng. 1984;13:221-46. doi: 10.1146/annurev.bb.13.060184.001253.
9
Single channel analysis of the inward rectifier K current in the rabbit ventricular cells.兔心室肌细胞内向整流钾电流的单通道分析
Jpn J Physiol. 1983;33(6):1039-56. doi: 10.2170/jjphysiol.33.1039.
10
Conductance properties of single inwardly rectifying potassium channels in ventricular cells from guinea-pig heart.豚鼠心室肌细胞中单个内向整流钾通道的电导特性
J Physiol. 1984 Feb;347:641-57. doi: 10.1113/jphysiol.1984.sp015088.

细胞内镁对豚鼠单个心房肌细胞毒蕈碱钾通道电流的双重作用。

Dual effects of intracellular magnesium on muscarinic potassium channel current in single guinea-pig atrial cells.

作者信息

Horie M, Irisawa H

机构信息

National Institute for Physiological Sciences, Okazaki, Japan.

出版信息

J Physiol. 1989 Jan;408:313-32. doi: 10.1113/jphysiol.1989.sp017461.

DOI:10.1113/jphysiol.1989.sp017461
PMID:2778732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1190405/
Abstract
  1. The effects of internal Mg2+ ions on the muscarinic acetylcholine (ACh) receptor-mediated K+ currents were investigated in single atrial cells of guinea-pigs, using the whole-cell and inside-out modes of the patch-clamp technique. 2. During cell dialysis in the whole-cell-clamp condition, the depletion of internal Mg2+ increased outward muscarinic K+ currents but decreased inward currents, thereby reducing the inwardly rectifying property of the channels. 3. When inside-out patches were prepared, channel availability was abolished and was reactivated by internal application of guanosine 5'-triphosphate (GTP) or its non-hydrolysable analogue, 5'-guanylyl imidodiphosphate (GppNHp), in the presence of Mg2+. GppNHp led to a recovery of the channels also in the nominal absence of Mg2+ (0[Mg2+]i). 4. The activation of single-channel currents by intracellular GTP and Mg2+ was dose-dependent. Both concentration-response curves were fitted by saturation kinetics with Hill coefficients of 1, and the half-maximum doses were 24 +/- 8 microM for GTP and 67 +/- 14 microM for Mg2+. The effects of Mg2+ on activation of K+ currents were additive with those of GTP, suggesting the presence of two independent binding sites for GTP and Mg2+. 5. The single-channel conductance became virtually ohmic when measured at nominally zero [Mg2+]i while GppNHp was used to recover the channel activity. Micromolar [Mg2+]i reduced the unitary amplitude of single open-channel currents in a dose- and voltage-dependent manner, showing half-blocking doses of 293 microM at +40 mV and 115 microM at +60 mV. 6. Voltage-dependent kinetics of Mg2+ block were described using equations based on Eyring rate theory (Woodbury, 1971; Hille, 1984), where the coefficient for voltage dependence (delta) was 0.63. 7. Intracellular Mg2+, at a physiological concentration, has a dual action on the muscarinic K+ channel: first Mg2+ activates the channel in the presence of GTP through GTP-binding proteins (G proteins), and secondly it blocks outward currents through the channel, thereby causing the inwardly rectifying property.
摘要
  1. 采用膜片钳技术的全细胞和内面向外模式,研究了细胞内镁离子(Mg2+)对豚鼠单个心房细胞中毒蕈碱型乙酰胆碱(ACh)受体介导的钾电流的影响。2. 在全细胞钳制条件下进行细胞透析时,细胞内Mg2+的耗竭增加了外向毒蕈碱型钾电流,但降低了内向电流,从而降低了通道的内向整流特性。3. 制备内面向外膜片时,通道可用性被消除,在Mg2+存在的情况下,通过向胞内施加鸟苷5'-三磷酸(GTP)或其不可水解类似物5'-鸟苷酰亚胺二磷酸(GppNHp)可使其重新激活。在名义上不存在Mg2+(0[Mg2+]i)的情况下,GppNHp也能使通道恢复。4. 细胞内GTP和Mg2+对单通道电流的激活呈剂量依赖性。两条浓度-反应曲线均符合饱和动力学,希尔系数为1,GTP的半最大剂量为24±8μM,Mg2+的半最大剂量为67±14μM。Mg2+对钾电流激活的作用与GTP的作用具有加和性,表明存在两个独立的GTP和Mg2+结合位点。5. 当在名义上为零的[Mg2+]i下测量且使用GppNHp恢复通道活性时,单通道电导实际上变为线性。微摩尔浓度的[Mg2+]i以剂量和电压依赖性方式降低单通道开放电流的单位幅度,在+40 mV时半阻断剂量为293μM,在+60 mV时为115μM。6. 使用基于艾林速率理论的方程(Woodbury,1971;Hille,1984)描述了Mg2+阻断的电压依赖性动力学,其中电压依赖性系数(δ)为0.63。7. 生理浓度的细胞内Mg2+对毒蕈碱型钾通道具有双重作用:首先,Mg2+在GTP存在的情况下通过GTP结合蛋白(G蛋白)激活通道;其次,它阻断通过通道向外的电流,从而导致内向整流特性。