Synaptic terminals in the dorsal lateral geniculate nucleus from neurons of the thalamic reticular nucleus: A light and electron microscope autoradiographic study

Neuroscience ◽  
1981 ◽  
Vol 6 (12) ◽  
pp. 2561-2577 ◽  
Author(s):  
V.M. Montero ◽  
G.L. Scott
2020 ◽  
Vol 124 (2) ◽  
pp. 404-417 ◽  
Author(s):  
Peter W. Campbell ◽  
Gubbi Govindaiah ◽  
Sean P. Masterson ◽  
Martha E. Bickford ◽  
William Guido

The thalamic reticular nucleus (TRN) modulates thalamocortical transmission through inhibition. In mouse, TRN terminals in the dorsal lateral geniculate nucleus (dLGN) form synapses with relay neurons but not interneurons. Stimulation of TRN terminals in dLGN leads to a frequency-dependent form of inhibition, with higher rates of stimulation leading to a greater suppression of spike firing. Thus, TRN inhibition appears more dynamic than previously recognized, having a graded rather than an all-or-none impact on thalamocortical transmission.


2002 ◽  
Vol 19 (4) ◽  
pp. 511-520 ◽  
Author(s):  
T. FITZGIBBON

Cells of the cat's perigeniculate nucleus (PGN), part of the visual sector of the thalamic reticular nucleus (TRN), provide GABAergic inhibition to the A and A1 layers of the dorsal lateral geniculate nucleus (LGNd) and, therefore, may control information flow from the retina to the cortex. Previous electrophysiological experiments suggested that the PGN may be subdivided on the basis of ocular dominance thus reflecting the afferent and efferent projections with lamina A and A1 of the LGNd. The present study utilized the ability of wheat germ agglutinin-horseradish peroxidase (WGA-HRP) to be transported transneuronally following intraocular injections in four cats to examine whether there is any anatomical evidence for eye specific layers within the PGN. Sections were processed with tetramethylbenzidine. Light WGA-HRP transneuronal labeling of LGNd collaterals and somata were seen in the PGN and very light labeling (but not somata) was seen in the TRN. Neither the cells of the PGN projecting to the LGNd nor the LGNd relay collaterals within the PGN were clearly organized into nonoverlapping laminae related to the eye specific layers of the LGNd. However, parts of the PGN immediately adjacent to the LGNd appear devoid of connections with lamina A1 thus creating a thin monocular segment for the contralateral eye.


1990 ◽  
Vol 228 (3) ◽  
pp. 327-338
Author(s):  
Ramón Carmona ◽  
Ruth Calvente ◽  
Francisco Abadía-Molina ◽  
Francisco Abadía-Fenoll

1994 ◽  
Vol 11 (4) ◽  
pp. 675-681 ◽  
Author(s):  
Vicente M. Montero

AbstractA postembedding immunogold procedure was used on thin sections of the dorsal lateral geniculate nucleus (LGN) and perigeniculate nucleus (PGN) of the cat to estimate qualitatively and quantitatively, at the electron-microscopic (EM) level, the intensity of glutamate or aspartate immunoreactivities on identifiable synaptic terminals and other profiles of the neuropil. On sections incubated with a glutamate antibody, terminals of retinal and cortical axons in the LGN, and of collaterals of geniculo-cortical axons in the PGN, contain significantly higher density of immunogold particles than GABAergic terminals, glial cells, dendrites, and cytoplasm of geniculate cells. By contrast, in sections incubated with an aspartate antibody, terminals of retino-geniculate, cortico-geniculate, and geniculo-cortical axons did not show a selective enrichment of immunoreactivity, but instead the density of immunogold particles was generally low in the different profiles of the neuropil, with the exception of nucleoli. These results suggest that glutamate, but not aspartate, is a neurotransmitter candidate in the retino-geniculo-cortical pathways.


Author(s):  
E. Vázquez-Ortíz ◽  
A. Ríos ◽  
J.L. Caballero

We have determined the regression equations that rule the behaviour of the dependent variable, the area occupied by the synaptic vesicles, as a function of the independent variable, the area of the profile, for those profiles corresponding to the RLP, RSD, FI AND F2 synaptic terminals in the α sector of the dorsal lateral geniculate nucleus (dLGN) of the rabbit. The ultrastructural characteristics (Fig.1) are similar to those described by other authors in the cat and the monkey.The rabbits used in this study were bred in captivity and were not albinos. After fixation by perfusion, the diencephalon was separated from the brain and cylinders were extracted with a 300 μm-diameter hypodermic needle in dorsoventral, anteroposterior and lateromedial directions. In this way we were able to obtain a set of samples distributed strategically throughout the α sector of the geniculate nucleus (α external dorsal, α external ventral, α external anterior, α external posterior, α external lateral and a internal regions, Fig. 2). The diencephalon and the extracted cylinders were treated in the normal ways for optical and electron microscopy, respectively.


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