Literature DB >> 803517

Lamination and differential distribution of thalamic afferents within the sensory-motor cortex of the squirrel monkey.

E G Jones.   

Abstract

The structure of the first somatic sensory area (areas 3, 1 and 2), of the motor area (area 4) and the intervening transitional field (area 3a) is described in the squirrel monkey (Saimiri sciureus) using Nissl, Bodian, Weil and Golgi preparations. The laminar arrangement of both cells and axons is briefly described and this correlated with the distribution of thalamic afferents as identified in experiments conducted with the Nauta and autoradiographic techniques. The latter method was used particularly in order to assess quantitative differences in the density of thalamic projections to the five cytoarchitectonic fields. In the somatic sensory areas thalamic afferents terminate not only in layer IV but a large extent also in a recognizable part of layer III (layer IIIb). In area 4 thalamic terminals fill much of layer III, reaching almost to layer II. In area 3a the extent is intermediate between that seen in areas 3 and 4. It is thought that the extensive spread of thalamic terminals is related to the elongated form of a particular class of spine-bearing cell whose somata are situated in layer IV (Jones, '75). In all areas a small proportion of thalamic afferents end also in layer I. Evidence is presented to indicate that specific afferent fibers emanating from the ventrobasal and ventrolateral complexes of the thalamus terminate in both the deep and superficial parts of layer I while "non-specific" afferents from other thalamic sources end in the superficial part. The autoradiographic studies indicate that there are considerable differences between the number of thalamic afferents ending in area 3 on the one hand and in areas 1 and 2 on the other. Given this and the nature of the degenerating thalamic afferents observed in Nauta preparations, it is possible to identify thalamic afferents in normal Golgi preparations and significant differences are detectable in areas 4, 3 and 1 and 2. It it is as yet uncertain whether the slightly thinner, more sparsely distributed thalamic afferents ending in areas 1 and 2 are branches of those directed primarily to area 3.

Entities:  

Mesh:

Year:  1975        PMID: 803517     DOI: 10.1002/cne.901600203

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  35 in total

1.  Periodicity and firing rate as candidate neural codes for the frequency of vibrotactile stimuli.

Authors:  E Salinas; A Hernandez; A Zainos; R Romo
Journal:  J Neurosci       Date:  2000-07-15       Impact factor: 6.167

2.  Thalamic relay nuclei of the basal ganglia form both reciprocal and nonreciprocal cortical connections, linking multiple frontal cortical areas.

Authors:  Nikolaus R McFarland; Suzanne N Haber
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

3.  Top-down laminar organization of the excitatory network in motor cortex.

Authors:  Nicholas Weiler; Lydia Wood; Jianing Yu; Sara A Solla; Gordon M G Shepherd
Journal:  Nat Neurosci       Date:  2008-02-03       Impact factor: 24.884

4.  Synaptic interactions between forelimb-related motor cortex neurons in behaving primates.

Authors:  W S Smith; E E Fetz
Journal:  J Neurophysiol       Date:  2009-05-13       Impact factor: 2.714

5.  Disordered plasticity in the primary somatosensory cortex in focal hand dystonia.

Authors:  Yohei Tamura; Yoshino Ueki; Peter Lin; Sherry Vorbach; Tatsuya Mima; Ryusuke Kakigi; Mark Hallett
Journal:  Brain       Date:  2009-01-16       Impact factor: 13.501

6.  Patterns of projections from area 2 of the sensory cortex to area 3a and to the motor cortex in cats.

Authors:  L L Porter
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

7.  Neocortical layers I and II of the hedgehog (Erinaceus europaeus). II. Thalamo-cortical connections.

Authors:  F Valverde; J A de Carlos; L López-Mascaraque; F Doñate-Oliver
Journal:  Anat Embryol (Berl)       Date:  1986

8.  Optical imaging of cortical networks via intracortical microstimulation.

Authors:  Andrea A Brock; Robert M Friedman; Reuben H Fan; Anna W Roe
Journal:  J Neurophysiol       Date:  2013-09-11       Impact factor: 2.714

9.  Connectivity of somatosensory cortical area 1 forms an anatomical substrate for the emergence of multifinger receptive fields and complex feature selectivity in the squirrel monkey (Saimiri sciureus).

Authors:  Mária Ashaber; Emese Pálfi; Robert M Friedman; Cory Palmer; Balázs Jákli; Li Min Chen; Orsolya Kántor; Anna W Roe; László Négyessy
Journal:  J Comp Neurol       Date:  2014-06-01       Impact factor: 3.215

10.  Anterolateral Motor Cortex Connects with a Medial Subdivision of Ventromedial Thalamus through Cell Type-Specific Circuits, Forming an Excitatory Thalamo-Cortico-Thalamic Loop via Layer 1 Apical Tuft Dendrites of Layer 5B Pyramidal Tract Type Neurons.

Authors:  KuangHua Guo; Naoki Yamawaki; Karel Svoboda; Gordon M G Shepherd
Journal:  J Neurosci       Date:  2018-08-24       Impact factor: 6.167

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.