The effects of gamma-aminobutyric acid (GABA) and related compounds were examined on longitudinal and circular muscle preparations isolated from oviducts of virgin rabbits. GABA and baclofen stimulated the spontaneous motility in each type of preparation, which action could not be antagonized by bicuculline, phentolamine, atropine or tetrodotoxin. Muscimol was virtually ineffective. Our results indicate the presence of GABAB receptors in the rabbit oviductal musculature which mediate the contractile response.
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http://dx.doi.org/10.1016/0014-2999(84)90141-9 | DOI Listing |
J Physiol
January 2025
Université Paris Cité, CNRS, ENS Paris Saclay, Centre Borelli UMR 9010, Paris, France.
Terminal Schwann cells (TSCs) are capable of regulating acetylcholine (ACh) release at the neuromuscular junction (NMJ). We have identified GABA as a gliotransmitter at mouse NMJs. When ACh activates α7 nicotinic ACh receptor (nAChRs) on TSCs, GABA is released and activates GABA receptors on the nerve terminal that subsequently reduce ACh release.
View Article and Find Full Text PDFJ Comput Neurosci
December 2024
Department of Applied Mathematics, and Centre for Theoretical Neuroscience, University of Waterloo, 200 University Avenue W, Waterloo, N2L 3G1, ON, Canada.
Sci Adv
December 2024
Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.
Hippocampus
October 2024
Institute for Integrative Neuroanatomy, Charité-Universitätmedizin Berlin, Berlin, Germany.
The processing of rich synaptic information in the dentate gyrus (DG) relies on a diverse population of inhibitory GABAergic interneurons to regulate cellular and circuit activity, in a layer-specific manner. Metabotropic GABA-receptors (GABARs) provide powerful inhibition to the DG circuit, on timescales consistent with behavior and learning, but their role in controlling the activity of interneurons is poorly understood with respect to identified cell types. We hypothesize that GABARs display cell type-specific heterogeneity in signaling strength, which will have direct ramifications for signal processing in DG networks.
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