Literature DB >> 7410613

Somatotopographic organization in the second somatosensory area of M. fascicularis.

C J Robinson, H Burton.   

Abstract

The second somatosensory area (SII) of awake, untrained cynomolgus monkeys was surveyed with recordings from nearly 1,000 single neurons. A detailed somatotopographic organization could be demonstrated in SII because the majority of these neurons had contralateral, moderate to well-defined receptive fields of < 10 cm2, and because neighboring neurons possessed receptive fields that were only slightly displaced from one another. Different body regions were represented in successive anterior to posterior strips that were oriented across the parietal operculum with an anterolateral to posteromedial slant. Neurons with trigeminal receptive fields were found in the anterior portion of SII; these neurons were the only ones in SII with predominantly bilateral receptive fields (r.f.'s.). Neurons with digit or hand r.f'.s form the largest component of the map, and were located posterior to those with face r.f.s. Most of these neurons had only contralateral activation. The hand and digit region was followed in turn by the arm, the upper and lower trunk, and the hindlimb regions. Although the overall SII orientation was along an anterior-posterior gradient, recordings at individual coronal planes often demonstrated isolated sequences of receptive fields that exhibited a medial-lateral progression. The principle example of this latter gradient was seen in the forelimb region where digits one through five were represented in an overlapping sequence across the parietal operculum. Except for portions of the digit representation, neighboring sequences of neurons in SII do not form a precise topologic map of the body that is comparable to the somatotopic maps observed in areas 3b and 1. The present findings contrast with previous physiological studies of SII in the primate. These discrepancies are discussed in relation to methodological differences and in terms of distinctions used to define the boundaries of SII.

Entities:  

Mesh:

Year:  1980        PMID: 7410613     DOI: 10.1002/cne.901920104

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


  49 in total

1.  The topography of tactile learning in humans.

Authors:  J A Harris; I M Harris; M E Diamond
Journal:  J Neurosci       Date:  2001-02-01       Impact factor: 6.167

2.  Phase locking between human primary and secondary somatosensory cortices.

Authors:  Cristina Simões; Ole Jensen; Lauri Parkkonen; Riitta Hari
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-21       Impact factor: 11.205

3.  Structural and functional analyses of human cerebral cortex using a surface-based atlas.

Authors:  D C Van Essen; H A Drury
Journal:  J Neurosci       Date:  1997-09-15       Impact factor: 6.167

4.  Functional organization of the insula and inner perisylvian regions.

Authors:  Ahmad Jezzini; Fausto Caruana; Ivilin Stoianov; Vittorio Gallese; Giacomo Rizzolatti
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-30       Impact factor: 11.205

5.  Localization and responses of neurones in the parieto-insular vestibular cortex of awake monkeys (Macaca fascicularis).

Authors:  O J Grüsser; M Pause; U Schreiter
Journal:  J Physiol       Date:  1990-11       Impact factor: 5.182

6.  Receptive field properties of the macaque second somatosensory cortex: evidence for multiple functional representations.

Authors:  Paul J Fitzgerald; John W Lane; Pramodsingh H Thakur; Steven S Hsiao
Journal:  J Neurosci       Date:  2004-12-08       Impact factor: 6.167

7.  The sensory insular cortex mediates the stress-buffering effects of safety signals but not behavioral control.

Authors:  John P Christianson; Alexander M Benison; Joshua Jennings; Emilee K Sandsmark; Jose Amat; Richard D Kaufman; Michael V Baratta; Evan D Paul; Serge Campeau; Linda R Watkins; Daniel S Barth; Steven F Maier
Journal:  J Neurosci       Date:  2008-12-10       Impact factor: 6.167

8.  Posterior insular cortex is necessary for conditioned inhibition of fear.

Authors:  Allison R Foilb; Johanna G Flyer-Adams; Steven F Maier; John P Christianson
Journal:  Neurobiol Learn Mem       Date:  2016-08-11       Impact factor: 2.877

9.  Large-scale expansion of the face representation in somatosensory areas of the lateral sulcus after spinal cord injuries in monkeys.

Authors:  Shashank Tandon; Niranjan Kambi; Leslee Lazar; Hisham Mohammed; Neeraj Jain
Journal:  J Neurosci       Date:  2009-09-23       Impact factor: 6.167

10.  The spinothalamic system targets motor and sensory areas in the cerebral cortex of monkeys.

Authors:  Richard P Dum; David J Levinthal; Peter L Strick
Journal:  J Neurosci       Date:  2009-11-11       Impact factor: 6.167

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.