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PMID: 6288177 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

GABA and bicuculline actions on mouse spinal cord and cortical neurons in cell culture.

Brain research ·Vol. 244 ·No. 1 ·1982-07-22 ·Pages 155-64

Nowak LM, Young AB, Macdonald RL

Abstract

The neutral amino acid gamma-aminobutyric acid (GABA) produced membrane hyperpolarization and increased membrane chloride ion conductance of spinal cord (SC) and cortical (CTX) neurons in cell culture. GABA dose-response curves were obtained for SC neurons by pressure applying known concentrations of GABA from micropipettes with large tips (miniperfusion pipettes). GABA response threshold was about 2 micrometers and large responses were elicited at GABA concentrations greater than 10 micrometers. Bicuculline (BICUC) (0.1-10 micrometers) reversibly antagonized GABA responses on both SC and CTX neurons with a half maximal inhibitory concentration of about 1 micrometer. BICUC antagonism of GABA responses was competitive (Lineweaver-Burke analysis). These results are compared with data on GABA and BICUC displacement of [3H]GABA binding to membranes of SC and CTX neurons in cell culture. It is suggested that high affinity GABA receptors are likely to be relevant for postsynaptic GABA responses while low affinity GABA receptors may be presynaptic.

MeSH Terms
Animals Bicuculline/pharmacology Cells, Cultured Cerebral Cortex/drug effects Dose-Response Relationship, Drug GABA Antagonists Membrane Potentials/drug effects Mice Neurons/drug effects Receptors, Cell Surface/drug effects Receptors, GABA-A Spinal Cord/drug effects gamma-Aminobutyric Acid/pharmacology
Chemicals
GABA Antagonists Receptors, Cell Surface Receptors, GABA-A gamma-Aminobutyric Acid Bicuculline
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nowak L M
Young A B
Macdonald R L
Article Info
Journal
Brain research
Abbr.
Brain Res
ISSN
0006-8993
Published
1982-07-22
Pages
155-64
Language
English
Region
Netherlands
NLM ID
0045503
Subset
IM
Grants
PHS HHS · 14279 · United States
NINDS NIH HHS · NS 15140 · United States
NINDS NIH HHS · NS 15225 · United States
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