Postsynaptic gephyrin immunoreactivity exhibits a nearly one‐to‐one correspondence with gamma‐aminobutyric acid‐like immunogold‐labeled synaptic inputs to sympathetic preganglionic neurons
- 5 June 1995
- journal article
- research article
- Published by Wiley in Journal of Comparative Neurology
- Vol. 356 (3) , 418-432
- https://doi.org/10.1002/cne.903560309
Abstract
Peripheral regulation of cardiovascular function is fundamentally influenced by central excitation and inhibition of sympathetic preganglionic neurons in thoracic spinal cord. This electron microscopy study investigated whether the γ‐aminobutyric acid (GABA)‐ergic and glycinergic inhibitory innervation of sympathetic preganglionic neurons arises from mutually exclusive afferent populations. Sympathetic preganglionic neurons were retrogradely labeled with cholera β subunit. GABAergic terminals were identified using strict quantitative statistical analyses as those boutons containing significantly elevated levels of GABA‐like immunogold labeling (GABA+). Glycinergic terminals were classified as those boutons opposite postsynaptic gephyrin immunostaining containing background levels of GABA‐like immunogold labeling (gephyrin+/GABA− association). Approximately 43% of the synaptic terminals that contacted sympathetic preganglionic somata and proximal dendrites and that were opposite gephyrin were GABA−; the remaining 57% were GABA+. Only two GABA+ boutons (4%) that synapsed on identified sympathetic preganglionic neuron (SPN) processes were not opposite gephyrin immunostaining (GABA+/gephyrin‐ association). GABA− /gephyrin+ associations were anticipated given prior anatomical, physiological, and pharmacological data. The observed nearly one‐to‐one correspondence between postsynaptic gephyrin immunoreactivity and GABA+ boutons was unexpected. Prior physiological and pharmacological experiments suggest that the postsynaptic effects of GABAergic inputs to sympathetic preganglionic neurons are mediated by activation of GABAA receptors. Those data, the present results, and other molecular, biochemical, and anatomical studies of gephyrin in the central nervous system (CNS) are consistent with two hypotheses: (1) Postsynaptic gephyrin is associated with GABAA receptors in the membranes of sympathetic preganglionic neurons, and (2) GABA+/gephyrin+ associations do not necessarily predict colocalization of GABA and glycine within single boutons synapsing on sympathetic preganglionic somata and dendrites.Keywords
This publication has 55 references indexed in Scilit:
- Assembly of the inhibitory glycine receptor: Identification of amino acid sequence motifs governing subunit stoichiometryNeuron, 1993
- Colocalization of neurotransmitters in the deep cerebellar nucleiJournal of Neurocytology, 1993
- Fast inhibitory postsynaptic potentials and responses to inhibitory amino acids of sympathetic preganglionic neurons in the adult catJournal of the Autonomic Nervous System, 1992
- Heterogeneity of receptor immunoreactivity at synapses of glycine-utilizing neuronsProceedings Of The Royal Society B-Biological Sciences, 1992
- Development of glycine receptor alpha subunit in cultivated rat spinal neurons: An immunocytochemical studyNeuroscience Letters, 1992
- Immuno-electronmicroscopic studies on the gamma-aminobutyric acid and glycine receptor in the intermediolateral nucleus of the thoracic spinal cord of rats and guinea pigsJournal of the Autonomic Nervous System, 1991
- Connectivity of glycine immunoreactive amacrine cells in the cat retinaJournal of Comparative Neurology, 1991
- Cloning of a glycine receptor subtype expressed in rat brain and spinal cord during a specific period of neuronal developmentFEBS Letters, 1991
- Glycinergic contacts in the outer plexiform layer of the Xenopus laevis retina characterized by antibodies to glycine, GABA, and glycine receptorsJournal of Comparative Neurology, 1990
- Preganglionic sympathetic neurones innervating the rat adrenal medulla: immunocytochemical evidence of synaptic input from nerve terminals containing substance P, GABA or 5-hydroxytryptamineJournal of the Autonomic Nervous System, 1988