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Mixed GABA–glycine synapses delineate a specific topography in the nucleus tractus solitarii of adult rat
Author(s) -
Dufour Amandine,
Tell Fabien,
Kessler JeanPierre,
Baude Agnès
Publication year - 2010
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2009.184838
Subject(s) - axon , inhibitory postsynaptic potential , neuroscience , glycine receptor , glycine , brainstem , electrophysiology , solitary nucleus , nucleus , axon terminal , sensory system , chemistry , biology , biochemistry , amino acid
Using combined morphological and electrophysiological approaches, we have determined the composition of inhibitory synapses of the nucleus tractus solitarii (NTS), a brainstem structure that is a gateway for many visceral sensory afferent fibres. Immunohistochemical experiments demonstrate that, in adult rat, GABA axon terminals are present throughout the NTS while mixed GABA–glycine axon terminals are strictly located to the lateral part of the NTS within subnuclei surrounding the tractus solitarius. Purely glycine axon terminals are rare in the lateral part of the NTS and hardly detected in its medial part. Electrophysiological experiments confirm the predominance of GABA inhibition throughout the NTS and demonstrate the existence of a dual inhibition involving the co‐release of GABA and glycine restricted to the lateral part of NTS. Since GABA A and glycine receptors are co‐expressed postsynaptically in virtually all the inhibitory axon terminals throughout the NTS, it suggests that the inhibition phenotype relies on the characteristics of the axon terminals. Our results also demonstrate that glycine is mostly associated with GABA within axon terminals and raise the possibility of a dynamic regulation of GABA/glycine release at the presynaptic level. Our data provide new information for understanding the mechanisms involved in the processing of visceral information by the central nervous system in adult animals.