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Publication : Molecular and functional diversity of GABA-A receptors in the enteric nervous system of the mouse colon.

First Author  Seifi M Year  2014
Journal  J Neurosci Volume  34
Issue  31 Pages  10361-78
PubMed ID  25080596 Mgi Jnum  J:215774
Mgi Id  MGI:5606234 Doi  10.1523/JNEUROSCI.0441-14.2014
Citation  Seifi M, et al. (2014) Molecular and functional diversity of GABA-A receptors in the enteric nervous system of the mouse colon. J Neurosci 34(31):10361-78
abstractText  The enteric nervous system (ENS) provides the intrinsic neural control of the gastrointestinal tract (GIT) and regulates virtually all GI functions. Altered neuronal activity within the ENS underlies various GI disorders with stress being a key contributing factor. Thus, elucidating the expression and function of the neurotransmitter systems, which determine neuronal excitability within the ENS, such as the GABA-GABAA receptor (GABAAR) system, could reveal novel therapeutic targets for such GI disorders. Molecular and functionally diverse GABAARs modulate rapid GABAergic-mediated regulation of neuronal excitability throughout the nervous system. However, the cellular and subcellular GABAAR subunit expression patterns within neurochemically defined cellular circuits of the mouse ENS, together with the functional contribution of GABAAR subtypes to GI contractility remains to be determined. Immunohistochemical analyses revealed that immunoreactivity for the GABAAR gamma (gamma) 2 and alphas (alpha) 1, 2, 3 subunits was located on somatodendritic surfaces of neurochemically distinct myenteric plexus neurons, while being on axonal compartments of submucosal plexus neurons. In contrast, immunoreactivity for the alpha4-5 subunits was only detected in myenteric plexus neurons. Furthermore, alpha-gamma2 subunit immunoreactivity was located on non-neuronal interstitial cells of Cajal. In organ bath studies, GABAAR subtype-specific ligands had contrasting effects on the force and frequency of spontaneous colonic longitudinal smooth muscle contractions. Finally, enhancement of gamma2-GABAAR function with alprazolam reversed the stress-induced increase in the force of spontaneous colonic contractions. The study demonstrates the molecular and functional diversity of the GABAAR system within the mouse colon providing a framework for developing GABAAR-based therapeutics in GI disorders.
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