Central-type benzodiazepines inhibit release of α-melanocyte-stimulating hormone from the rat hypothalamus
- 1 January 1991
- journal article
- Published by Elsevier in Neuroscience
- Vol. 42 (2) , 509-516
- https://doi.org/10.1016/0306-4522(91)90393-3
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- Importance of a novel GABAA receptor subunit for benzodiazepine pharmacologyNature, 1989
- A pyridazinyl derivative of gamma-aminobutyric acid (GABA), SR 95531, is a potent antagonist of Cl− channel opening regulated by GABAA receptorsNeuropharmacology, 1987
- Pyridazinyl-GABA derivatives: a new class of synthetic GABAA antagonistsTrends in Pharmacological Sciences, 1986
- The effect of benzodiazepines and β-carbolines on gabastimulated chloride influx by membrane vesicles from the rat cerebral cortexBiochemical and Biophysical Research Communications, 1986
- Immunological characterization of endorphins, adrenocorticotropin, and melanotropins in frog hypothalamusGeneral and Comparative Endocrinology, 1983
- Immunocytochemical localization of ACTH perikarya in nucleus tractus solitarius: evidence for a second opiocortin neuronal systemNeuroscience Letters, 1983
- GABA Neuron Systems in Hypothalamus and the Pituitary GlandNeuroendocrinology, 1982
- α-MSH in rat brain: occurence within and outside of β-endorphin neuronsBrain Research, 1980
- Nucleotide sequence of cloned cDNA for bovine corticotropin-β-lipotropin precursorNature, 1979
- Pharmacological characterization of different types of GABA and glutamate receptors in vertebrates and invertebrates☆☆☆Progress in Neurobiology, 1979