Literature DB >> 14689472

Cytoarchitecture and cortical connections of the posterior cingulate and adjacent somatosensory fields in the rhesus monkey.

R J Morecraft1, P B Cipolloni, K S Stilwell-Morecraft, M T Gedney, D N Pandya.   

Abstract

The cytoarchitecture and connections of the caudal cingulate and medial somatosensory areas were investigated in the rhesus monkey. There is a stepwise laminar differentiation starting from retrosplenial area 30 towards the isocortical regions of the medial parietal cortex. This includes a gradational emphasis on supragranular laminar organization and general reduction of the infragranular neurons as one proceeds from area 30 toward the medial parietal regions, including areas 3, 1, 2, 5, 31, and the supplementary sensory area (SSA). This trend includes a progressive increase in layer IV neurons. Area 23c in the lower bank and transitional somatosensory area (TSA) in the upper bank of the cingulate sulcus appear as nodal points. From area 23c and TSA the architectonic progression can be traced in three directions: one culminates in areas 3a and 3b (core line), the second in areas 1, 2, and 5 (belt line), and the third in areas 31 and SSA (root line). These architectonic gradients are reflected in the connections of these regions. Thus, cingulate areas (30, 23a, and 23b) are connected with area 23c and TSA on the one hand and have widespread connections with parieto-temporal, frontal, and parahippocampal (limbic) regions on the other. Area 23c has connections with areas 30, 23a and b, and TSA as well as with medial somatosensory areas 3, 1, 2, 5, and SSA. Area 23c also has connections with parietotemporal, frontal, and limbic areas similar to areas 30, 23a, and 23b. Area TSA, like area 23c, has connections with areas 3, 1, 2, 5, and SSA. However, it has only limited connections with the parietotemporal and frontal regions and none with the parahippocampal gyrus. Medial area 3 is mainly connected to medial and dorsal sensory areas 3, 1, 2, 5, and SSA and to areas 4 and 6 as well as to supplementary (M2 or area 6m), rostral cingulate (M3 or areas 24c and d), and caudal cingulate (M4 or areas 23c and d) motor cortices. Thus, in parallel with the architectonic gradient of laminar differentiation, there is also a progressive shift in the pattern of corticocortical connections. Cingulate areas have widespread connections with limbic, parietotemporal, and frontal association areas, whereas parietal area 3 has more restricted connections with adjacent somatosensory and motor cortices. TSA is primarily related to the somatosensory-motor areas and has limited connections with the parietotemporal and frontal association cortices. Copyright 2003 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2004        PMID: 14689472     DOI: 10.1002/cne.10980

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


  73 in total

1.  Architecture and neurocytology of monkey cingulate gyrus.

Authors:  Brent A Vogt; Leslie Vogt; Nuri B Farber; George Bush
Journal:  J Comp Neurol       Date:  2005-05-09       Impact factor: 3.215

2.  Navigation-associated medial parietal neurons in monkeys.

Authors:  Nobuya Sato; Hideo Sakata; Yuji L Tanaka; Masato Taira
Journal:  Proc Natl Acad Sci U S A       Date:  2006-10-26       Impact factor: 11.205

3.  Characterization of some morphological parameters of orbicularis oculi motor neurons in the monkey.

Authors:  D W McNeal; J Ge; J L Herrick; K S Stilwell-Morecraft; R J Morecraft
Journal:  Neuroscience       Date:  2007-07-17       Impact factor: 3.590

4.  Evidence for direct projections from the basal nucleus of the amygdala to retrosplenial cortex in the Macaque monkey.

Authors:  J A Buckwalter; C M Schumann; G W Van Hoesen
Journal:  Exp Brain Res       Date:  2007-11-30       Impact factor: 1.972

5.  Thalamic projections to the posteromedial cortex in the macaque.

Authors:  Joseph A Buckwalter; Josef Parvizi; Robert J Morecraft; Gary W van Hoesen
Journal:  J Comp Neurol       Date:  2008-04-10       Impact factor: 3.215

6.  Posterior cingulate and retrosplenial cortex connections of the caudal superior temporal region in the rhesus monkey.

Authors:  Benjamin Seltzer; Deepak N Pandya
Journal:  Exp Brain Res       Date:  2009-04-21       Impact factor: 1.972

7.  Hemifacial motor and crying seizures of temporal lobe onset: case report and review of electro-clinical localisation.

Authors:  R E Hogan; V K Rao
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-01       Impact factor: 10.154

8.  Treatment with Mesenchymal-Derived Extracellular Vesicles Reduces Injury-Related Pathology in Pyramidal Neurons of Monkey Perilesional Ventral Premotor Cortex.

Authors:  Maria Medalla; Wayne Chang; Samantha M Calderazzo; Veronica Go; Alexandra Tsolias; Joseph W Goodliffe; Dhruba Pathak; Diego De Alba; Monica Pessina; Douglas L Rosene; Benjamin Buller; Tara L Moore
Journal:  J Neurosci       Date:  2020-04-02       Impact factor: 6.167

9.  Precuneus shares intrinsic functional architecture in humans and monkeys.

Authors:  Daniel S Margulies; Justin L Vincent; Clare Kelly; Gabriele Lohmann; Lucina Q Uddin; Bharat B Biswal; Arno Villringer; F Xavier Castellanos; Michael P Milham; Michael Petrides
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-10       Impact factor: 11.205

10.  Cytoarchitecture and cortical connections of the anterior insula and adjacent frontal motor fields in the rhesus monkey.

Authors:  R J Morecraft; K S Stilwell-Morecraft; J Ge; P B Cipolloni; D N Pandya
Journal:  Brain Res Bull       Date:  2015-10-20       Impact factor: 4.077

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.