1999
DOI: 10.1002/(sici)1096-9861(19991129)414:4<454::aid-cne3>3.0.co;2-7
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Distribution pattern of inhibitory and excitatory synapses in the dendritic tree of single masseter ?-motoneurons in the cat

Abstract: Little is known about the differences in the distributions of inhibitory and excitatory synapses in the dendritic tree of single motoneurons in the brainstem and spinal cord. In this study, the distribution of γ‐aminobutyric acid (GABA)‐, glycine‐, and glutamate‐like immunoreactivity in axon terminals on dendrites of cat masseter α‐motoneurons, stained intracellularly with horseradish peroxidase, was examined by using postembedding immunogold histochemistry in serial ultrathin sections. The dendritic tree was … Show more

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Cited by 58 publications
(42 citation statements)
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“…Apparently, MMNs and DMNs receive GABAergic inputs that are weaker than glycinergic inputs from the SupV. The number of glycine-immunoreactive boutons synapsing on MMNs and DMNs in cats is close to twice the number of GABA-immunoreactive boutons (Bae et al 1999;Shigenaga et al 2005). The SupV may be the origin of glycinergic and GABAergic axon terminals at MMNs and DMNs.…”
Section: Glycinergic and Gabaergic Inputs From The Supv To The Movmentioning
confidence: 94%
“…Apparently, MMNs and DMNs receive GABAergic inputs that are weaker than glycinergic inputs from the SupV. The number of glycine-immunoreactive boutons synapsing on MMNs and DMNs in cats is close to twice the number of GABA-immunoreactive boutons (Bae et al 1999;Shigenaga et al 2005). The SupV may be the origin of glycinergic and GABAergic axon terminals at MMNs and DMNs.…”
Section: Glycinergic and Gabaergic Inputs From The Supv To The Movmentioning
confidence: 94%
“…Two lines of evidence support this contention. First, both Hcrt and glutamatecontaining presynaptic terminals are found within the V motor nucleus (Bae et al 1999;Fung et al 2001). Second, Hcrt has been shown to modulate amino acids release.…”
Section: Interaction Of Glutamate and Hypocretinmentioning
confidence: 99%
“…To date, the location and distribution of synapses on neurons that have been morphologically analyzed have been determined by processes such as electron microscopy (EM; Bae et al, 1999; Megias et al, 2001; Shigenaga et al, 2005; Arthur et al, 2007; Chen et al, 2008b), or by light microscopy of cultured neurons. However, these techniques are limited by the lack of three-dimensional morphology of the entire post-synaptic neuron, replete with all of the surrounding cellular inputs in its physiological setting [e.g., cultured neurons; (Cullen et al, 2010; Ivenshitz and Segal, 2010; Schatzle et al, 2012)], as well as the limited and labor-intensive nature of being able to identify the synaptic type, including the molecular make up of its postsynaptic specialization [i.e., neurotransmitter type or post-synaptic adaptor proteins, as in EM analyses; (Chen et al, 2008b; Dani et al, 2010)].…”
Section: Introductionmentioning
confidence: 99%