Common pharmacological and physico-chemical properties of 5-HT3 binding sites in the rat cerebral cortex and NG 108-15 clonal cells
- 1 October 1990
- journal article
- research article
- Published by Elsevier in Biochemical Pharmacology
- Vol. 40 (7) , 1541-1550
- https://doi.org/10.1016/0006-2952(90)90452-q
Abstract
No abstract availableKeywords
This publication has 41 references indexed in Scilit:
- Characterization of [3H]Quipazine Binding to 5‐Hydroxytryptamine3 Receptors in Rat Brain MembranesJournal of Neurochemistry, 1989
- 5-HT3 receptors are membrane ion channelsNature, 1989
- Electrophysiology of 5-HT3 receptors in neuronal cell linesTrends in Pharmacological Sciences, 1989
- Interactions between dopamine and 5-HT3 receptors suggest new treatments for psychosis and drug addictionTrends in Pharmacological Sciences, 1989
- 5-HT3 receptors mediate inhibition of acetylcholine release in cortical tissueNature, 1989
- Identification of 5-HT3 recognition sites in human brain tissue using [3H]zacoprideJournal of Pharmacy and Pharmacology, 1988
- 5-HT3 receptors mediate rapid responses in cultured hippocampus and a clonal cell lineNeuron, 1988
- [3H]Zacopride: Ligand for the Identification of 5-HT3 Recognition SitesJournal of Pharmacy and Pharmacology, 1988
- Identification and distribution of 5-HT3 receptors in rat brain using radioligand bindingNature, 1987
- The pharmacology and function of 5-HT3receptorsTrends in Neurosciences, 1986