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PMID: 1691468 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Antagonism of 5-HT3 receptor mediated currents in murine N1E-115 neuroblastoma cells by (+)-tubocurarine.

Neuroscience letters ·Vol. 110 ·No. 1-2 ·1990-03-02 ·Pages 107-12

Peters JA, Malone HM, Lambert JJ

Abstract

5-HT3 receptor-mediated membrane currents were recorded from voltage-clamped clonal N1E-115 neuroblastoma cells. The inward current response to ionophoretically applied serotonin (5-HT) was reversibly antagonised by the 5-HT3 receptor antagonists GR 38032F and metoclopramide with IC50 values of 0.2 nM and 14 nM, respectively. Low concentrations of (+)-tubocurarine [+)-Tc) also blocked the response to 5-HT (IC50 = 0.8 nM), but other nicotinic cholinoceptor antagonists (gallamine, vecuronium and trimetaphan) were ineffective when applied at a relatively high concentration (1 microM). Blockade by (+)-Tc was neither voltage- nor use-dependent, suggesting that (+)-Tc does not block 5-HT-activated ion channels in N1E-115 cells.

MeSH Terms
Animals Cell Line Imidazoles/pharmacology Ion Channels/drug effects,physiology Membrane Potentials/drug effects Mice Neuroblastoma Neurons/drug effects,physiology Ondansetron Receptors, Nicotinic/drug effects Receptors, Serotonin/drug effects,physiology Serotonin Antagonists Tubocurarine/pharmacology
Chemicals
Imidazoles Ion Channels Receptors, Nicotinic Receptors, Serotonin Serotonin Antagonists Ondansetron Tubocurarine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Peters J A
Department of Pharmacology and Clinical Pharmacology, Ninewells Hospital, Dundee, U.K.
Malone H M
Lambert J J
Article Info
Journal
Neuroscience letters
Abbr.
Neurosci Lett
ISSN
0304-3940
Published
1990-03-02
Pages
107-12
Language
English
Region
Ireland
NLM ID
7600130
Subset
IM
Grants
Wellcome Trust · United Kingdom
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