Literature DB >> 6090181

Proconflict effect of benzodiazepine receptor inverse agonists and other inhibitors of GABA function.

E N Petersen, L H Jensen.   

Abstract

GABA seems to be a neurotransmitter with great impact on conflict behaviour in rats. We studied the effects of different types of GABA function inhibitors on conflict behaviour in rats. Among these inhibitors, the benzodiazepine (BZ) receptor inverse agonists are a new type of compound downregulating GABA-mediated functions allosterically. The most effective proconflict inducing compounds were pentylenetetrazol and the three BZ inverse agonists beta-CCM, beta-CCE and ZK 90886. The BZ receptor inverse agonists, FG 7142, DMCM and CGS 8216, the GABA antagonist bicuculline and the GABA synthesis inhibitor isoniazid were moderately active. Only a weak effect was seen with just subconvulsive doses of picrotoxin, a chloride channel inhibitor. These results show that the mode of GABA function inhibition determines the degree to which proconflict action is elicited and that proconflict effects and proconvulsant or convulsant effects may be separated. Evidence is presented that proconflict action in rats is predictive of an anxiogenic action in man.

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Year:  1984        PMID: 6090181     DOI: 10.1016/0014-2999(84)90193-6

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  18 in total

1.  Anxiogenic drugs beta-CCE and FG 7142 increase extracellular dopamine levels in nucleus accumbens.

Authors:  L D McCullough; J D Salamone
Journal:  Psychopharmacology (Berl)       Date:  1992       Impact factor: 4.530

2.  Safety signal withdrawal: a behavioural paradigm sensitive to both "anxiolytic" and "anxiogenic" drugs under identical experimental conditions.

Authors:  M H Thiébot; L Dangoumau; G Richard; A J Puech
Journal:  Psychopharmacology (Berl)       Date:  1991       Impact factor: 4.530

3.  The benzodiazepine antagonist CGS 8216 decreases both shocked and unshocked drinking in rats.

Authors:  D J Sanger
Journal:  Psychopharmacology (Berl)       Date:  1987       Impact factor: 4.530

4.  GABAergic drugs and conflict behavior in the rat: lack of similarities with the actions of benzodiazepines.

Authors:  A Agmo; R Pruneda; M Guzmán; M Gutiérrez
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1991-09       Impact factor: 3.000

5.  Evaluation of the muscle relaxant properties of a novel beta-carboline, ZK 93423 in rats and cats.

Authors:  T Klockgether; I Pardowitz; M Schwarz; K H Sontag; L Turski
Journal:  Br J Pharmacol       Date:  1985-10       Impact factor: 8.739

Review 6.  Anxiogenic properties of beta-CCE and FG 7142: a review of promises and pitfalls.

Authors:  M H Thiébot; P Soubrié; D Sanger
Journal:  Psychopharmacology (Berl)       Date:  1988       Impact factor: 4.530

7.  Post-training administration of GABAergic antagonists enhances retention of aversively motivated tasks.

Authors:  J D Brioni; J L McGaugh
Journal:  Psychopharmacology (Berl)       Date:  1988       Impact factor: 4.530

8.  LY 171555-induced hyperdefensiveness in the mouse does not implicate benzodiazepine receptors.

Authors:  C Belzung; S Cabib; L Fabiani; P Tolentino; S Puglisi-Allegra
Journal:  Psychopharmacology (Berl)       Date:  1991       Impact factor: 4.530

9.  Beta-carbolines can enhance or antagonize the effects of punishment in mice.

Authors:  D N Stephens; W Kehr
Journal:  Psychopharmacology (Berl)       Date:  1985       Impact factor: 4.530

10.  Human studies on abecarnil a new beta-carboline anxiolytic: safety, tolerability and preliminary pharmacological profile.

Authors:  T Duka; B Schütt; W Krause; R Dorow; S McDonald; K Fichte
Journal:  Br J Clin Pharmacol       Date:  1993-04       Impact factor: 4.335

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