Literature DB >> 3933600

The effects of methyl beta-carboline-3-carboxylate on social interaction and locomotor activity when microinjected into the nucleus raphé dorsalis of the rat.

S W Hindley, A Hobbs, I A Paterson, M H Roberts.   

Abstract

Intraperitoneal and intracerebral injections of methyl beta-carboline-3-carboxylate (beta CCM) and intracerebral injections of RO 15-1788 were given to rats. The performance of the rats in the social interaction test was measured to determine if changes in social interaction induced by beta CCM were mediated in part by the nucleus raphé dorsalis (NRD). Intraperitoneal injections of beta CCM, 2 and 4 mg kg-1, reduced social interaction. Intracerebral microinjections of beta CCM (10-0.1 ng in 0.5 microliter) into the NRD reduced social interaction. Injections outside the NRD did not have this effect. Intracerebral microinjections of RO 15-1788 (1 ng in 0.5 microliters) into the NRD had no effect when given alone, but blocked the reduction in social interaction caused by intracerebral or intraperitoneal injections of beta CCM. No effect was observed when R 15-1788 was microinjected into sites outside the NRD. Changes in social interaction may reflect changes in anxiety. The NRD may be one of the important sites for the expression of the anxiogenic actions of beta CCM.

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Year:  1985        PMID: 3933600      PMCID: PMC1916738          DOI: 10.1111/j.1476-5381.1985.tb08955.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  17 in total

1.  Benzodiazepines: potentiation of a GABA inhibitory response in the dorsal raphe nucleus.

Authors:  D W Gallager
Journal:  Eur J Pharmacol       Date:  1978-05-15       Impact factor: 4.432

2.  Localization of the site of the anticonflict action of benzodiazepines in the amygdaloid nucleus of rats.

Authors:  K Shibata; Y Kataoka; Y Gomita; S Ueki
Journal:  Brain Res       Date:  1982-02-25       Impact factor: 3.252

3.  The use of social interaction as a method for detecting anxiolytic activity of chlordiazepoxide-like drugs.

Authors:  S E File
Journal:  J Neurosci Methods       Date:  1980-06       Impact factor: 2.390

4.  GABA reduces binding of 3H-methyl beta-carboline-3-carboxylate to brain benzodiazepine receptors.

Authors:  C Braestrup; M Nielsen
Journal:  Nature       Date:  1981-12-03       Impact factor: 49.962

5.  The anxiogenic action of benzodiazepine antagonists.

Authors:  S E File; R G Lister; D J Nutt
Journal:  Neuropharmacology       Date:  1982-10       Impact factor: 5.250

6.  Effects of GABA and diazepam on 3H-serotonin release from hippocampal synaptosomes.

Authors:  D J Balfour
Journal:  Eur J Pharmacol       Date:  1980-11-07       Impact factor: 4.432

Review 7.  Minor tranquilizers and brain defense systems.

Authors:  F G Graeff
Journal:  Braz J Med Biol Res       Date:  1981-10       Impact factor: 2.590

Review 8.  Benzodiazepine receptor ligands with positive and negative efficacy.

Authors:  C Braestrup; M Nielsen; T Honoré; L H Jensen; E N Petersen
Journal:  Neuropharmacology       Date:  1983-12       Impact factor: 5.250

9.  Attenuation of induced-anxiety in rats by chlordiazepoxide: role of raphe dorsalis benzodiazepine binding sites and serotoninergic neurons.

Authors:  M H Thiébot; M Hamon; P Soubríe
Journal:  Neuroscience       Date:  1982       Impact factor: 3.590

10.  Benzodiazepines: anxiety-reducing activity by reduction of serotonin turnover in the brain.

Authors:  C D Wise; B D Berger; L Stein
Journal:  Science       Date:  1972-07-14       Impact factor: 47.728

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