Literature DB >> 3108929

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

D J Sanger.   

Abstract

Previous studies of the benzodiazepine antagonist CGS 8216 have reported that this compound may enhance the punishment-induced suppression of behaviour. In order to investigate this phenomenon further, water-deprived rats were trained to drink from a water spout during a multiple schedule with shocked and unshocked components. During the shocked components a very mild electric footshock was presented after every 20th lick. The shock slightly reduced the rate of licking during these components below that which occurred during periods without shock, although this effect decreased during the experiment. CGS 8216 (0.3-10 mg/kg) produced a dose-related reduction in licking during both schedule components. The overall volumes of water consumed were reduced by CGS 8216 as was the number of licks during the first, unshocked schedule component, before shock was applied, showing that the effect on unshocked licking was not due to a generalisation of suppression between periods with or without shock. In contrast to CGS 8216, a dose of 10 mg/kg pentylenetetrazol selectively reduced shocked licking. In a second group of rats which drank under identical conditions but without shock, CGS 8216 again reduced water intake. These results show that CGS 8216 can reduce water intake in rats regardless of whether drinking results in shock presentation.

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Year:  1987        PMID: 3108929     DOI: 10.1007/bf00216015

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  22 in total

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Authors:  E RODIN
Journal:  Electroencephalogr Clin Neurophysiol       Date:  1958-08

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Journal:  J Med Chem       Date:  1982-04       Impact factor: 7.446

4.  Proconvulsant action of CGS 8216.

Authors:  S E File
Journal:  Neurosci Lett       Date:  1983-03-14       Impact factor: 3.046

5.  Do benzodiazepine receptors mediate the anticonflict action of pentobarbital?

Authors:  W B Mendelson; T Davis; S M Paul; P Skolnick
Journal:  Life Sci       Date:  1983-05-09       Impact factor: 5.037

6.  Effects of the benzodiazepine antagonist Ro 15-1788 on social and agonistic behaviour in male albino mice.

Authors:  R J Rodgers; A J Waters
Journal:  Physiol Behav       Date:  1984-09

7.  Intracranial self-stimulation distinguishes between two benzodiazepine antagonists.

Authors:  S Pellow; S E File; L J Herberg
Journal:  Neurosci Lett       Date:  1984-06-15       Impact factor: 3.046

Review 8.  The neuropharmacology of various diazepam antagonists.

Authors:  C A Boast; P S Bernard; B S Barbaz; K M Bergen
Journal:  Neuropharmacology       Date:  1983-12       Impact factor: 5.250

9.  CGS 8216: receptor binding characteristics of a potent benzodiazepine antagonist.

Authors:  A J Czernik; B Petrack; H J Kalinsky; S Psychoyos; W D Cash; C Tsai; R K Rinehart; F R Granat; R A Lovell; D E Brundish; R Wade
Journal:  Life Sci       Date:  1982-01-25       Impact factor: 5.037

10.  Chlordiazepoxide-induced hyperphagia in non-food-deprived rats: effects of Ro15-1788, CGS 8216 and ZK 93 426.

Authors:  S J Cooper; W R Moores
Journal:  Eur J Pharmacol       Date:  1985-05-28       Impact factor: 4.432

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  2 in total

1.  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

Review 2.  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

  2 in total

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