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Calcium channels: molecular pharmacology, structure and regulation.

作者信息

Hosey M M, Lazdunski M

机构信息

Department of Biological Chemistry and Structure, Chicago Medical School, Illinois 60064.

出版信息

J Membr Biol. 1988 Sep;104(2):81-105. doi: 10.1007/BF01870922.

DOI:10.1007/BF01870922
PMID:2903935
Abstract
摘要

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本文引用的文献

1
G proteins as regulators of ion channel function.作为离子通道功能调节因子的G蛋白。
Trends Neurosci. 1987 Jun 1;10(6):241-244. doi: 10.1016/0166-2236(87)90166-4.
2
Slow inward barium current and contraction on frog single muscle fibres.青蛙单根肌纤维上的缓慢内向钡电流和收缩
J Physiol. 1980 Jun;303:91-109. doi: 10.1113/jphysiol.1980.sp013273.
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Release of acetylcholine from rat brain synaptosomes stimulated with leptinotarsin, a new neurotoxin.
J Neurochem. 1980 Mar;34(3):635-42. doi: 10.1111/j.1471-4159.1980.tb11191.x.
调控植物钙离子信号的药理学策略。
Int J Mol Sci. 2018 May 18;19(5):1506. doi: 10.3390/ijms19051506.
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T-Type Calcium Channel: A Privileged Gate for Calcium Entry and Control of Adrenal Steroidogenesis.T型钙通道：钙内流及肾上腺类固醇生成调控的特殊通道
Front Endocrinol (Lausanne). 2016 May 20;7:43. doi: 10.3389/fendo.2016.00043. eCollection 2016.
5
Effects of L-type Calcium Channel Antagonists Verapamil and Diltiazem on fKv1.4ΔN Currents in Xenopus oocytes.L型钙通道拮抗剂维拉帕米和地尔硫䓬对非洲爪蟾卵母细胞中fKv1.4ΔN电流的影响。
Iran J Pharm Res. 2013 Fall;12(4):855-66.
6
Cytoplasmic calcium affects the gating of potassium channels in the plasma membrane ofChara corallina: a whole-cell study using calcium-channel effectors.细胞质钙影响 Chara corallina 质膜钾通道的门控：使用钙通道效应物的全细胞研究。
Planta. 1990 Mar;180(4):569-81. doi: 10.1007/BF02411456.
7
Tracheary-element differentiation in suspension-cultured cells ofZinnia requires uptake of extracellular Ca(2+) : Experiments with calcium-channel blockers and calmodulin inhibitors.悬浮培养的百日草细胞中的导管分子分化需要细胞外 Ca(2+) 的摄取：使用钙离子通道阻滞剂和钙调蛋白抑制剂的实验。
Planta. 1990 Mar;180(4):502-9. doi: 10.1007/BF02411447.
8
Comparative analysis of calcium spikes upon activation of serotonin(1A) and purinergic receptors.比较分析血清素（1A）和嘌呤能受体激活时钙峰的变化。
PLoS One. 2012;7(12):e51857. doi: 10.1371/journal.pone.0051857. Epub 2012 Dec 19.
9
Robust anti-arrhythmic efficacy of verapamil and flunarizine against dofetilide-induced TdP arrhythmias is based upon a shared and a different mode of action.维拉帕米和氟桂利嗪对多非利特诱导的 Tdp 心律失常具有强大的抗心律失常作用，其作用机制既有共同之处，也有不同之处。
Br J Pharmacol. 2010 Sep;161(1):162-75. doi: 10.1111/j.1476-5381.2010.00883.x.
10
Effects of flavoxate hydrochloride on voltage-dependent Ba2+ currents in human detrusor myocytes at different experimental temperatures.盐酸黄酮哌酯在不同实验温度下对人逼尿肌细胞电压依赖性Ba2+电流的影响。
Naunyn Schmiedebergs Arch Pharmacol. 2007 Nov;376(3):195-203. doi: 10.1007/s00210-007-0190-6. Epub 2007 Oct 2.
4
Overcoming of vincristine resistance in P388 leukemia in vivo and in vitro through enhanced cytotoxicity of vincristine and vinblastine by verapamil.通过维拉帕米增强长春新碱和长春碱的细胞毒性在体内和体外克服P388白血病对长春新碱的耐药性
Cancer Res. 1981 May;41(5):1967-72.
5
Effect of glycerol treatment on the calcium current of frog skeletal muscle.甘油处理对青蛙骨骼肌钙电流的影响。
J Physiol. 1980 Aug;305:87-96. doi: 10.1113/jphysiol.1980.sp013351.
6
Leptinotarsin: a presynaptic neurotoxin that stimulates release of acetylcholine.
Proc Natl Acad Sci U S A. 1980 Feb;77(2):1219-23. doi: 10.1073/pnas.77.2.1219.
7
Characterization of binding of the Ca++ channel antagonist, [3H]nitrendipine, to guinea-pig ileal smooth muscle.钙离子通道拮抗剂[3H]尼群地平与豚鼠回肠平滑肌结合的特性研究
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8
A venom peptide with a novel presynaptic blocking action.一种具有新型突触前阻断作用的毒液肽。
Nature. 1984;308(5956):282-4. doi: 10.1038/308282a0.
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Passive transfer of Lambert-Eaton myasthenic syndrome with IgG from man to mouse depletes the presynaptic membrane active zones.将患兰伯特－伊顿肌无力综合征患者的IgG被动转移至小鼠体内，会使突触前膜活性区减少。
Proc Natl Acad Sci U S A. 1983 Dec;80(24):7636-40. doi: 10.1073/pnas.80.24.7636.
10
A unitary mechanism of calcium antagonist drug action.钙拮抗剂药物作用的单一机制。
Proc Natl Acad Sci U S A. 1983 Feb;80(3):860-4. doi: 10.1073/pnas.80.3.860.