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Benzodiazepine receptor ligands with opposing pharmacologic actions.

作者信息

Petrack B, Czernik A J, Cassidy J P, Bernard P, Yokoyama N

出版信息

Adv Biochem Psychopharmacol. 1983;38:129-37.

PMID:6142600
Abstract
摘要

相似文献

1
Benzodiazepine receptor ligands with opposing pharmacologic actions.具有相反药理作用的苯二氮䓬受体配体。
Adv Biochem Psychopharmacol. 1983;38:129-37.
2
Interactions of different ligand classes with the benzodiazepine receptor.不同配体类别与苯二氮䓬受体的相互作用。
Adv Biochem Psychopharmacol. 1983;38:65-72.
3
[Benzodiazepines and benzodiazepine receptors].[苯二氮䓬类药物与苯二氮䓬受体]
Eksp Med Morfol. 1986;25(1):46-50.
4
Benzodiazepine receptor number after acute administration of alprazolam and diazepam.
Res Commun Chem Pathol Pharmacol. 1982 Feb;35(2):229-35.
5
Ro 16-6028: a novel anxiolytic acting as a partial agonist at the benzodiazepine receptor.
Pharmacopsychiatry. 1988 Nov;21(6):360-2. doi: 10.1055/s-2007-1021947.
6
Benzodiazepines receptor binding in vivo: pharmacokinetic and pharmacological significance.体内苯二氮䓬受体结合：药代动力学和药理学意义
Adv Biochem Psychopharmacol. 1983;38:189-99.
7
[11C-Ro15-1788 and 11C-flunitrazepam, two coordinates for the study by positron emission tomography of benzodiazepine binding sites].[11C-Ro15-1788和11C-氟硝西泮，用于通过正电子发射断层扫描研究苯二氮䓬结合位点的两个坐标]
C R Seances Acad Sci III. 1983;296(18):871-6.
8
The action of stress, beta-carbolines, diazepam, and Ro 15-1788 on GABA receptors in the rat brain.
Adv Biochem Psychopharmacol. 1983;38:105-19.
9
Chronic RO 15-1788 treatment increases the number of benzodiazepine receptors in rat cerebral cortex and hippocampus.长期使用RO 15-1788治疗可增加大鼠大脑皮层和海马体中苯二氮䓬受体的数量。
Eur J Pharmacol. 1983 May 20;90(1):125-8. doi: 10.1016/0014-2999(83)90223-6.
10
Differential modulation of etazolate or pentobarbital enhanced [3H] muscimol binding by benzodiazepine agonists and inverse agonists.依托唑啉或戊巴比妥增强的[³H]蝇蕈醇结合受苯二氮䓬激动剂和反向激动剂的差异调节。
Brain Res. 1983 Dec 5;280(2):383-6. doi: 10.1016/0006-8993(83)90072-0.

引用本文的文献

1
Pharmacokinetics and clinical use of flumazenil (Ro 15-1788).氟马西尼（Ro 15 - 1788）的药代动力学及临床应用
Clin Pharmacokinet. 1988 Jan;14(1):1-12. doi: 10.2165/00003088-198814010-00001.
2
The affinities, potencies and efficacies of some benzodiazepine-receptor agonists, antagonists and inverse-agonists at rat hippocampal GABAA-receptors.某些苯二氮䓬受体激动剂、拮抗剂及反向激动剂对大鼠海马γ-氨基丁酸A（GABAA）受体的亲和力、效能和效力
Br J Pharmacol. 1987 Jul;91(3):601-8. doi: 10.1111/j.1476-5381.1987.tb11253.x.
3
A 7-phenyl substituted triazolopyridazine has inverse agonist activity at the benzodiazepine receptor site.
一种7-苯基取代的三唑并哒嗪在苯二氮䓬受体位点具有反向激动剂活性。
Br J Pharmacol. 1987 Jan;90(1):183-90. doi: 10.1111/j.1476-5381.1987.tb16839.x.
4
A beta-carboline antagonizes benzodiazepine actions but does not precipitate the abstinence syndrome in cats.
Psychopharmacology (Berl). 1985;86(1-2):132-6. doi: 10.1007/BF00431697.
5
Effects of non-sedative anxiolytic drugs on responses to GABA and on diazepam-induced enhancement of these responses on mouse neurones in cell culture.非镇静性抗焦虑药物对细胞培养的小鼠神经元中γ-氨基丁酸（GABA）反应以及地西泮诱导的这些反应增强的影响。
Br J Pharmacol. 1988 Sep;95(1):109-20. doi: 10.1111/j.1476-5381.1988.tb16554.x.