(Q48490405)

12 February 2018

title

The anxiolytic effect of gamma-hydroxybutyrate in the elevated plus maze is reversed by the benzodiazepine receptor antagonist, flumazenil (English)

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12 February 2018

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Schmidt-Mutter C

1

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12 February 2018

Pain L

2

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12 February 2018

Sandner G

3

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12 February 2018

Gobaille S

4

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12 February 2018

Maitre M

5

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12 February 2018

language of work or name

English

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publication date

1 January 1998

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12 February 2018

European Journal of Pharmacology

published in

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12 February 2018

volume

342

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12 February 2018

issue

1

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12 February 2018

page(s)

21-27

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12 February 2018

Naloxone blocks the antianxiety but not the motor effects of benzodiazepines and pentobarbital: experimental studies and literature review

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Neuropharmacology of a new potential anxiolytic compound, F 2692, 1-(3'-trifluoromethyl phenyl) 1,4-dihydro 3-amino 4-oxo 6-methyl pyridazine. 1. Acute and in vitro effects

7 January 2021

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The benzodiazepine antagonist flumazenil blocks the effects of CCK receptor agonists and antagonists in the elevated plus-maze

7 January 2021

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Diazepam binding inhibitor (DBI): a peptide with multiple biological actions

7 January 2021

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Conversion of γ-hydroxybutyrate to γ-aminobutyrate by mouse brain in vivo

7 January 2021

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Naloxone antagonizes ethanol- but not gamma-hydroxybutyrate-induced sleep in mice

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Effects of amperozide in two animal models of anxiety

7 January 2021

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The anxiolytic but not the sedative properties of tracazolate are reversed by the benzodiazepine receptor antagonist, Ro 15-1788.

7 January 2021

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Gamma-hydroxybutyric acid for treatment of opiate withdrawal syndrome.

7 January 2021

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Flumazenil effects on growth hormone response to gamma-hydroxybutyric acid.

7 January 2021

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Characterization of methionine-enkephalin release in the rat striatum by in vivo dialysis: effects of gamma-hydroxybutyrate on cellular and extracellular methionine-enkephalin levels.

7 January 2021

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gamma-Hydroxybutyrate uptake by rat brain striatal slices

7 January 2021

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Extracellular events induced by gamma-hydroxybutyrate in striatum: a microdialysis study.

7 January 2021

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Action of γ-hydroxybutyrate and GABA on neurones of cultured rat central nervous system

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Selective antagonists of benzodiazepines

7 January 2021

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Sodium 4-hydroxybutyrate

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7 January 2021

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Pharmacological profile of a potential anxiolytic: AP159, a new benzothieno-pyridine derivative

7 January 2021

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Validation of open:closed arm entries in an elevated plus-maze as a measure of anxiety in the rat

7 January 2021

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Kappa opioid agonists produce anxiolytic-like behavior on the elevated plus-maze

7 January 2021

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Vigabatrin has an anxiolytic effect in the elevated plus-maze test of anxiety

7 January 2021

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Anti-sedative and anti-cataleptic properties of NCS-382, a γ-hydroxybutyrate receptor antagonist

7 January 2021

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Failure of gamma-hydroxybutyrate to alter the function of the GABAA receptor complex in the rat cerebral cortex

7 January 2021

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GABA receptors in the region of the dorsomedial hypothalamus of rats regulate anxiety in the elevated plus-maze test. I. Behavioral measures.

7 January 2021

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Anxiolytic-like effect of the GABA-transaminase inhibitor vigabatrin (gamma-vinyl GABA) on rat exploratory activity.

7 January 2021

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Naloxone overcomes the dopaminergic, EEG, and behavioral effects of gamma-hydroxybutyrate

7 January 2021

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GABAA receptor function in the gamma-hydroxybutyrate model of generalized absence seizures

7 January 2021

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gamma-Hydroxybutyric acid binding sites: evidence for coupling to a chloride anion channel

7 January 2021

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γ-Hydroxybutyric acid binding sites: Interaction with the GABA-benzodiazepine-picrotoxin receptor complex

7 January 2021

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Involvement of the opioid system in the anxiolytic effect of diazepam in mice

7 January 2021

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Conversion of gamma-hydroxybutyrate to gamma-aminobutyrate in vitro

7 January 2021

1 reference

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Naloxone and metergoline effects on growth hormone response to gamma-hydroxybutyric acid.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2897%2901503-3

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0014-2999(97)01503-3

1 reference

12 February 2018

1 reference

12 February 2018