Functional coupling of GABAA receptors and benzodiazepine recognition site subtypes in the spinal cord of the rat
- 1 October 1989
- journal article
- research article
- Published by Elsevier in European Journal of Pharmacology
- Vol. 169 (2-3) , 205-213
- https://doi.org/10.1016/0014-2999(89)90017-4
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- γ‐Aminobutyric Acid and Pentobarbital Enhance 2‐[3H]Oxoquazepam Binding to Type I Benzodiazepine Recognition Sites in Rat and Human BrainJournal of Neurochemistry, 1988
- Preferential affinity of 3H-2-oxo-quazepam for type I benzodiazepine recognition sites in the human brainLife Sciences, 1988
- Selective affinity of the benzodiazepines quazepam and 2-oxo-quazepam for BZ1 binding site and demonstration of 3H-2-oxo-quazepam as a BZ1 selective radioligandLife Sciences, 1988
- Enhancement of γ‐Aminobutyric Acid Binding by Quazepam, a Benzodiazepine Derivative with Preferential Affinity for Type I Benzodiazepine ReceptorsJournal of Neurochemistry, 1986
- Benzodiazepine receptors in the human spinal cord: A detailed anatomical and pharmacological studyNeuroscience, 1986
- Postnatal Development of Proteins Associated with Different Benzodiazepine ReceptorsJournal of Neurochemistry, 1986
- Stress and β-carbolines decrease the density of low affinity gaba binding sitesBrain Research, 1984
- [3H]Propyl β‐Carboline‐3‐Carboxylate as a Selective Radioligand for the BZ1 Benzodiazepine Receptor SubclassJournal of Neurochemistry, 1981
- Molecular Mechanisms in the Receptor Action of BenzodiazepinesAnnual Review of Pharmacology and Toxicology, 1979
- Mathematical theory of complex ligand-binding systems at equilibrium: Some methods for parameter fittingAnalytical Biochemistry, 1972