某些钙拮抗剂是大鼠脑中[3H]苯环己哌啶（PCP）结合的强效置换剂。 - Suppr | 超能文献

Certain calcium antagonists are potent displacers of [3H]phencyclidine (PCP) binding in rat brain.

作者信息

Quirion R, Pert C B

出版信息

Eur J Pharmacol. 1982 Sep 10;83(1-2):155-6. doi: 10.1016/0014-2999(82)90305-3.

DOI:10.1016/0014-2999(82)90305-3

Abstract

摘要

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Certain calcium antagonists are potent displacers of [3H]phencyclidine (PCP) binding in rat brain.某些钙拮抗剂是大鼠脑中[3H]苯环己哌啶（PCP）结合的强效置换剂。

Eur J Pharmacol. 1982 Sep 10;83(1-2):155-6. doi: 10.1016/0014-2999(82)90305-3.

2

Tissue response selectivity of calcium antagonists is not due to heterogeneity of [3H]-nitrendipine binding sites.钙拮抗剂的组织反应选择性并非源于[3H]-尼群地平结合位点的异质性。

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Phencyclidine increases the affinity of dihydropyridine calcium channel antagonist binding in rat brain.苯环利定可增加大鼠脑中二氢吡啶钙通道拮抗剂结合的亲和力。

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Autoradiographic localization of a calcium channel antagonist, [3H]nitrendipine, binding site in rat brain.大鼠脑中钙通道拮抗剂[3H]尼群地平结合位点的放射自显影定位

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Enhancement of brain calcium antagonist binding by phencyclidine and related compounds.苯环利定及相关化合物对脑钙拮抗剂结合的增强作用。

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Mechanism of calcium channel blockade by verapamil, D600, diltiazem and nitrendipine in single dialysed heart cells.维拉帕米、D600、地尔硫䓬和尼群地平在单个透析心脏细胞中对钙通道的阻滞机制

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Effects of dihydropyridine calcium channel blocking drugs on rat brain muscarinic and alpha-adrenergic receptors.二氢吡啶类钙通道阻滞药对大鼠脑毒蕈碱受体和α-肾上腺素能受体的影响。

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Interaction of calcium channel blockers with non-neuronal benzodiazepine binding sites.钙通道阻滞剂与非神经元苯二氮䓬结合位点的相互作用。

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引用本文的文献

1

Phencyclidine in nanomolar concentrations binds to synaptosomes and blocks certain potassium channels.纳摩尔浓度的苯环利定与突触体结合并阻断某些钾通道。

Proc Natl Acad Sci U S A. 1983 Jun;80(12):3855-9. doi: 10.1073/pnas.80.12.3855.

2

Phencyclidine increases the affinity of dihydropyridine calcium channel antagonist binding in rat brain.苯环利定可增加大鼠脑中二氢吡啶钙通道拮抗剂结合的亲和力。

Naunyn Schmiedebergs Arch Pharmacol. 1985 Sep;330(3):227-34. doi: 10.1007/BF00572438.

3

Phencyclidine. Physiological actions, interactions with excitatory amino acids and endogenous ligands.苯环利定。生理作用、与兴奋性氨基酸及内源性配体的相互作用。

Mol Neurobiol. 1987 Fall;1(3):191-211. doi: 10.1007/BF02936608.