Literature DB >> 3530375

A chronic unit study of the sensory properties of neurons in the forelimb areas of rat sensorimotor cortex.

C F Sievert, E J Neafsey.   

Abstract

The sensory properties of neurons in the several forelimb areas of rat sensorimotor cortex were examined using the technique of extracellular single-unit recording in the awake, head-restrained rat. Cells with peripheral receptive fields were tested for the amount and modality of sensory input during joint manipulation and brushing and tapping of limbs, face and trunk. Input-output correlations were made on the basis of the results of receptive field mapping and intracortical microstimulation in the same electrode penetration. It was found that neurons (n = 117) in the rostral forelimb area receive virtually no sensory input while 30% of neurons (n = 114) in the caudal forelimb primary motor area do receive such input. The inputs to caudal forelimb motor area neurons were primarily (83%) from single joints; along perpendicular electrode penetrations the same joint that activated a cortical cell also moved when microstimulation was delivered along the same electrode penetration. In the granular and dysgranular zones of somatic sensory forelimb cortex, 70% of neurons (n = 82) were responsive to peripheral sensory inputs, with most of the cells in the granular cortex responsive to cutaneous inputs while cells in the dysgranular cortex were more responsive to deep inputs. The lack of sensory inputs to the rostral forelimb motor area is consistent with the proposal that this region may be a part of the supplementary motor area of the rat.

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Year:  1986        PMID: 3530375     DOI: 10.1016/0006-8993(86)90684-0

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  17 in total

1.  Cortical modulation of thalamo-cortical neurons relaying exteroceptive information: a microstimulation study in the guinea pig.

Authors:  C Rapisarda; A Palmeri; S Sapienza
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

2.  Early development of SI cortical barrel subfield representation of forelimb in normal and deafferented neonatal rat as delineated by peroxidase conjugated lectin, peanut agglutinin (PNA).

Authors:  R S Waters; C A McCandlish; N G Cooper
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

3.  Short-term reorganization of input-deprived motor vibrissae representation following motor disconnection in adult rats.

Authors:  Gianfranco Franchi; Carlo Veronesi
Journal:  J Physiol       Date:  2006-05-11       Impact factor: 5.182

Review 4.  Cortical Reorganization of Sensorimotor Systems and the Role of Intracortical Circuits After Spinal Cord Injury.

Authors:  Hisham Mohammed; Edmund R Hollis
Journal:  Neurotherapeutics       Date:  2018-07       Impact factor: 7.620

5.  Dynamic organization of primary motor cortex output to target muscles in adult rats. II. Rapid reorganization following motor nerve lesions.

Authors:  J P Donoghue; S Suner; J N Sanes
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

6.  Relationship between the organization of the forepaw barrel subfield and the representation of the forepaw in layer IV of rat somatosensory cortex.

Authors:  R S Waters; C X Li; C A McCandlish
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

7.  Rewiring of hindlimb corticospinal neurons after spinal cord injury.

Authors:  Arko Ghosh; Florent Haiss; Esther Sydekum; Regula Schneider; Miriam Gullo; Matthias T Wyss; Thomas Mueggler; Christof Baltes; Markus Rudin; Bruno Weber; Martin E Schwab
Journal:  Nat Neurosci       Date:  2009-12-13       Impact factor: 24.884

8.  Automated light-based mapping of motor cortex by photoactivation of channelrhodopsin-2 transgenic mice.

Authors:  Oliver G S Ayling; Thomas C Harrison; Jamie D Boyd; Alexander Goroshkov; Timothy H Murphy
Journal:  Nat Methods       Date:  2009-02-15       Impact factor: 28.547

9.  Reversible Inactivation of Rat Premotor Cortex Impairs Temporal Preparation, but not Inhibitory Control, During Simple Reaction-Time Performance.

Authors:  Nathaniel J Smith; Nicole K Horst; Benjamine Liu; Marcelo S Caetano; Mark Laubach
Journal:  Front Integr Neurosci       Date:  2010-10-08

Review 10.  Cortical reorganization after spinal cord injury: always for good?

Authors:  K A Moxon; A Oliviero; J Aguilar; G Foffani
Journal:  Neuroscience       Date:  2014-07-02       Impact factor: 3.590

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