Calcium-antagonist drugs. Receptor interactions that clarify therapeutic effects.

Suppr

超能文献

作者信息

Snyder S H, Reynolds I J

出版信息

N Engl J Med. 1985 Oct 17;313(16):995-1002. doi: 10.1056/NEJM198510173131606.

DOI:10.1056/NEJM198510173131606

PMID:2413355

Abstract

摘要

相似文献

Calcium-antagonist drugs. Receptor interactions that clarify therapeutic effects.

N Engl J Med. 1985 Oct 17;313(16):995-1002. doi: 10.1056/NEJM198510173131606.

Molecular properties of voltage-sensitive calcium channels.

Soc Gen Physiol Ser. 1987;41:201-13.

Phosphatidylinositol turnover as a functional probe for neuronal Ca2+ channels.

Prog Clin Biol Res. 1988;252:41-5.

Characterization of the calcium entry blocker receptor complex in cardiac sarcolemmal membrane vesicles.

Prog Clin Biol Res. 1988;252:29-34.

Conformational features of calcium channel agonist and antagonist analogs of nifedipine.

Mol Pharmacol. 1985 May;27(5):544-8.

Differential sensitivity of calcium channels to dihydropyridines. The modulated receptor hypothesis.钙通道对二氢吡啶的差异敏感性。调制受体假说。

Biochem Pharmacol. 1986 Dec 1;35(23):4115-20. doi: 10.1016/0006-2952(86)90684-2.

[3H]Phencyclidine interactions with the nicotinic acetylcholine receptor channel and its inhibition by psychotropic, antipsychotic, opiate, antidepressant, antibiotic, antiviral, and antiarrhythmic drugs.

Mol Pharmacol. 1982 Jul;22(1):72-81.

Molecular properties of structure and regulation of the calcium channel.钙通道的结构分子特性及调节

Ann N Y Acad Sci. 1988;522:134-49. doi: 10.1111/j.1749-6632.1988.tb33350.x.

L-type calcium channel blockade on haloperidol-induced c-Fos expression in the striatum.L型钙通道阻滞对氟哌啶醇诱导的纹状体c-Fos表达的影响

Neuroscience. 2007 Nov 9;149(3):602-16. doi: 10.1016/j.neuroscience.2007.08.013. Epub 2007 Aug 14.

[Research on receptors of calcium antagonists and the calcium channel].[钙拮抗剂的受体与钙通道研究]

Sheng Li Ke Xue Jin Zhan. 1988 Apr;19(2):155-60.

引用本文的文献

Calcium channel blockers for antipsychotic-induced tardive dyskinesia.用于抗精神病药物所致迟发性运动障碍的钙通道阻滞剂。

Cochrane Database Syst Rev. 2018 Mar 26;3(3):CD000206. doi: 10.1002/14651858.CD000206.pub4.

Differential inhibition of T-type calcium channels by neuroleptics.抗精神病药物对T型钙通道的差异性抑制作用

J Neurosci. 2002 Jan 15;22(2):396-403. doi: 10.1523/JNEUROSCI.22-02-00396.2002.

Current concepts of pharmacotherapy in hypertension: combination calcium channel blocker therapy in the treatment of hypertension.高血压药物治疗的当前概念：联合使用钙通道阻滞剂治疗高血压。

J Clin Hypertens (Greenwich). 2001 Sep-Oct;3(5):322-7. doi: 10.1111/j.1524-6175.2001.00484.x.

[Effect of changed extracellular K(+) and Mg(2+)-concentration on intracellular Ca(2+) homeostasis, contraction coupling and force-frequency relations in the human myocardium].

Herz. 1997 Jun;22 Suppl 1:18-27. doi: 10.1007/BF03042651.

Dopaminergic function in rat brain after oral administration of calcium-channel blockers or haloperidol. A microdialysis study.

J Neural Transm Gen Sect. 1994;95(3):195-207. doi: 10.1007/BF01271566.

In vitro effects of calcium entry blockers, chlorpromazine and fenoterol upon human pregnant myometrium contractility.钙通道阻滞剂、氯丙嗪和非诺特罗对人妊娠子宫肌层收缩力的体外作用。

Br J Pharmacol. 1986 Nov;89(3):515-23. doi: 10.1111/j.1476-5381.1986.tb11151.x.

A calcium blocking and anticholinergic agent (terodiline) in the treatment of detrusor hyperreflexia: a placebo-controlled, cross-over trial.一种钙阻滞剂和抗胆碱能药物（特罗地林）治疗逼尿肌反射亢进：一项安慰剂对照交叉试验

J Neurol Neurosurg Psychiatry. 1987 Oct;50(10):1331-6. doi: 10.1136/jnnp.50.10.1331.

Organic psychosis caused by diltiazem.地尔硫䓬引起的器质性精神病。

J R Soc Med. 1988 May;81(5):296-7. doi: 10.1177/014107688808100521.

Calcium and calmodulin antagonists inhibit human malaria parasites (Plasmodium falciparum): implications for drug design.钙和钙调蛋白拮抗剂抑制人类疟原虫（恶性疟原虫）：对药物设计的启示。

Proc Natl Acad Sci U S A. 1987 Oct;84(20):7310-4. doi: 10.1073/pnas.84.20.7310.

Thrombolytic treatment and new calcium antagonists.溶栓治疗与新型钙拮抗剂。

Br Med J (Clin Res Ed). 1988 Mar 5;296(6623):705-8. doi: 10.1136/bmj.296.6623.705.

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