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1.
Neurosci Behav Physiol ; 36(9): 929-40, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17024332

ABSTRACT

Morphometric studies of human forebrain formations composed of densely branched cells - the entorhinal cortex, the basolateral amygdala, the nucleus accumbens, the striatum, and the dorsal thalamus - were performed using nine parameters, with statistical analysis of the resulting data; measurements addressed the major projection-type densely branched and sparsely branched reticular neurons (scattered reticular and marginal reticular cells of the dorsal thalamus) stained by the Golgi method and with NADPH-diaphorase. Scattered reticular cells in the various formations showed no differences in any of the nine measures, while there were significant differences (in 5-7 measures, apart from one comparison, where there were differences in two measures) in their major projection-type densely branched cells. Scattered reticular and main projection-type densely branched neurons in each formation differed in terms of 7-9 measures. In endbrain formations, scattered reticular neurons contained NADPH-diaphorase; in the dorsal thalamus, only intermediate marginal reticular neurons were NADPH-diaphorase-positive. Thus, these human formations contained a common system of ancient integrative NADPH-diaphorase-containing reticular cells. Our results, along with published data, show these to be projection-type cells with projections to layers V and VI of the neocortex, which suggests that they have modulatory influences on its descending systems.


Subject(s)
NADPH Dehydrogenase/metabolism , Neurons/metabolism , Neurons/ultrastructure , Prosencephalon/cytology , Reticular Formation/physiology , Adult , Brain Mapping , Female , Humans , Male , Neural Pathways/physiology , Reticular Formation/cytology , Silver Staining/methods
2.
Bull Exp Biol Med ; 141(6): 657-61, 2006 Jun.
Article in English, Russian | MEDLINE | ID: mdl-17364042

ABSTRACT

The somatodendritic structure of projection neurons was morphometrically examined in the nucleus accumbens of human brain. In contrast to reticular neurons, spiny neurons of the nucleus accumbens and dorsal striatum have different somatodendritic structure. In both parts of the striatum, reticular neurons were NADPH-diaphorase-positive.


Subject(s)
Dendrites/ultrastructure , Neurons/cytology , Nucleus Accumbens/cytology , Dendrites/metabolism , Histocytochemistry , Humans , NADPH Dehydrogenase/metabolism , Silver Staining
3.
Zh Vyssh Nerv Deiat Im I P Pavlova ; 55(6): 798-811, 2005.
Article in Russian | MEDLINE | ID: mdl-16396486

ABSTRACT

Cell morphometry with statistical analysis (using 9 parameters) of densely branched projection and sparsely branched reticular neurons was performed in the human forebrain formations built from densely branched projection neurons (the entorhinal cortex, striatum, nucleus accumbens basolateral amygdala, and dorsal thalamus). The reticular neurons included scattered reticular neurons and marginal reticular neurons of the dorsal thalamus. Golgi method and staining for NADPH-diaphorase were used. The scattered reticular neurons of different formations under study did not differ in any of the 9 parameters, whereas they significantly differed from the main projection neurons in 5 to 7 parameters (except one comparison with the difference in 2 parameters). Within the same formation, the scattered reticular and main projection densely branched neurons differed in 7 to 9 parameters. The endbrain scattered reticular neurons expressed NADPH-diaphorase, while in the dorsal thalamus only the medium marginal reticular neurons were NADPH-diaphorase-positive. Thus, a common system of ancient integrative reticular neurons expressing NADPH-diaphorase exists in the examined human forebrain formations. The evidence obtained by us and the literature data point to the projection nature of the scattered reticular neurons (to the V and VI neocortical layers), which suggests their modulatory influence on descending neocortical pathways.


Subject(s)
Interneurons/enzymology , NADPH Dehydrogenase/analysis , Prosencephalon/cytology , Humans , Interneurons/cytology
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