Literature DB >> 40260

A synthetic non-benzodiazepine ligand for benzodiazepine receptors: a probe for investigating neuronal substrates of anxiety.

A S Lippa, J Coupet, E N Greenblatt, C A Klepner, B Beer.   

Abstract

CL 218,872 is the first non-benzodiazepine to selectively displace brain specific 3H-diazepam binding with a potency comparable to that of the benzodiazepines. Like the benzodiazepines, CL 218,872 increased punished responding in a conflict situation and protected against the convulsions induced by pentylenetetrazole. These three pharmacological properties are highly predictive of anxiolytic activity. Unlike the benzodiazepines, however, CL 218,872 was relatively inactive in tests designed to measure effects on neuronal systems which utilize GABA, glycine and serotonin as transmitters. Furthmore, CL 218,872 was relatively free of the ataxic and depressant side effects commonly associated with the benzodiazepines. Because of this high degree of selectivity, CL 218,872 may represent a new probe for investigating neuronal substrates of anxiety.

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Year:  1979        PMID: 40260     DOI: 10.1016/0091-3057(79)90304-6

Source DB:  PubMed          Journal:  Pharmacol Biochem Behav        ISSN: 0091-3057            Impact factor:   3.533


  34 in total

1.  Mechanism of action of the hypnotic zolpidem in vivo.

Authors:  F Crestani; J R Martin; H Möhler; U Rudolph
Journal:  Br J Pharmacol       Date:  2000-12       Impact factor: 8.739

2.  Involvement of GABAergic systems in benzodiazepine-induced impairment of passive avoidance learning in mice.

Authors:  K Tohyama; T Nabeshima; K Ichihara; T Kameyama
Journal:  Psychopharmacology (Berl)       Date:  1991       Impact factor: 4.530

3.  Effect of psychotomimetics and some putative anxiolytics on stress-induced hyperthermia.

Authors:  A Lecci; F Borsini; L Gragnani; G Volterra; A Meli
Journal:  J Neural Transm Gen Sect       Date:  1991

4.  Effects of non-sedative anxiolytic drugs on responses to GABA and on diazepam-induced enhancement of these responses on mouse neurones in cell culture.

Authors:  P P De Deyn; R L Macdonald
Journal:  Br J Pharmacol       Date:  1988-09       Impact factor: 8.739

5.  Discriminative stimulus effects of omega (BZ) receptor ligands: correlation with in vivo inhibition of [3H]-flumazenil binding in different regions of the rat central nervous system.

Authors:  D J Sanger; J Benavides
Journal:  Psychopharmacology (Berl)       Date:  1993       Impact factor: 4.530

6.  The sedative effects of CL 218,872, like those of chlordiazepoxide, are reversed by benzodiazepine antagonists.

Authors:  S E File; S Pellow; L Wilks
Journal:  Psychopharmacology (Berl)       Date:  1985       Impact factor: 4.530

7.  A comparison between chlordiazepoxide and CL 218,872--a synthetic nonbenzodiazepine ligand for benzodiazepine receptors on spontaneous locomotor activity in rats.

Authors:  J F McElroy; R L Fleming; R S Feldman
Journal:  Psychopharmacology (Berl)       Date:  1985       Impact factor: 4.530

8.  A comparison between chlordiazepoxide and CL 218,872, a synthetic non-benzodiazepine ligand for benzodiazepine receptors, on serotonin and catecholamine turnover in brain.

Authors:  J F McElroy; R S Feldman; J S Meyer
Journal:  Psychopharmacology (Berl)       Date:  1986       Impact factor: 4.530

9.  gamma-Aminobutyric acid type A receptor point mutation increases the affinity of compounds for the benzodiazepine site.

Authors:  D B Pritchett; P H Seeburg
Journal:  Proc Natl Acad Sci U S A       Date:  1991-02-15       Impact factor: 11.205

10.  Like diazepam, CL 218,872, a selective ligand for the benzodiazepine omega 1 receptor subtype, impairs place learning in the Morris water maze.

Authors:  R K McNamara; R W Skelton
Journal:  Psychopharmacology (Berl)       Date:  1992       Impact factor: 4.530

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