Literature DB >> 9658059

Corticoreticular pathways in the cat. I. Projection patterns and collaterization.

B Kably1, T Drew.   

Abstract

This paper summarizes and compares the projection patterns and the receptive fields of cortical neurons in areas 4 and 6 that project to the pontomedullary reticular formation (PMRF). A total of 326 neurons were recorded in area 4 and 129 in area 6 in four awake, unrestrained cats that were chronically implanted with arrays of electrodes in the PMRF and the pyramidal tract (PT). In area 4, 47% of the neurons projected to the caudal PT but not to the PMRF (PTNs); 19% were activated only from the PMRF [corticoreticular neurons (CRNs)], whereas 27% were activated from both the PT and the PMRF (PTN/CRNs). More PTN/CRNs conducted at velocities >20 m/s (82%) than did CRNs (23%). In area 6, only 19% of the neurons were identified as PTNs, 12% were PTN/CRNs and 31% were CRNs; a further 38% could not be activated from either structure. Collateral branches within the PMRF conducted at maximum velocities of 20 m/s (average = 6.5 m/s). No significant differences in the conduction velocities of the collateral branches were found either between fast and slow PTNs or between area 4 and area 6 neurons. A large proportion of neurons in area 4 (85/173, 49%) were activated by passive manipulation of the more distal, contralateral forelimb, with approximately equal numbers being classed as PTNs, PTN/CRNs and CRNs. Most neurons in area 6 for which a receptive field could be found were excited by lightly touching or tapping the face and neck; a receptive field could not be determined for 39% of the area 6 neurons compared with only 5% of those in area 4. Finally, there was evidence that neurons in quite widespread areas of the pericruciate cortex, including both areas 4 and 6 projected onto similar, restricted regions of the PMRF. The fact that the cortical projection from area 4 to the PMRF includes a high percentage of fast PTNs with a receptive field on the distal forelimb is consistent with the view that this projection may serve to integrate movement and the dynamic postural adjustments that accompany them. The fact that the cortical projection from area 6 to the PMRF is primarily from slow PTNs with receptive fields on the face, neck and back is consistent with a role for this cortical area in adjusting the general posture of the animal on which movements are superimposed.

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Year:  1998        PMID: 9658059     DOI: 10.1152/jn.1998.80.1.389

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  33 in total

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2.  Motor outputs from the primate reticular formation to shoulder muscles as revealed by stimulus-triggered averaging.

Authors:  Adam G Davidson; John A Buford
Journal:  J Neurophysiol       Date:  2004-03-10       Impact factor: 2.714

3.  Effects of combined cortical and acoustic stimuli on muscle activity.

Authors:  R J Fisher; A Sharott; A A Kühn; P Brown
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5.  Bilateral actions of the reticulospinal tract on arm and shoulder muscles in the monkey: stimulus triggered averaging.

Authors:  Adam G Davidson; John A Buford
Journal:  Exp Brain Res       Date:  2006-02-28       Impact factor: 1.972

Review 6.  How can corticospinal tract neurons contribute to ipsilateral movements? A question with implications for recovery of motor functions.

Authors:  Elzbieta Jankowska; Stephen A Edgley
Journal:  Neuroscientist       Date:  2006-02       Impact factor: 7.519

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Authors:  E Jankowska; K Stecina
Journal:  J Physiol       Date:  2007-01-25       Impact factor: 5.182

Review 8.  Plasticity of connections underlying locomotor recovery after central and/or peripheral lesions in the adult mammals.

Authors:  Serge Rossignol
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2006-09-29       Impact factor: 6.237

Review 9.  Sensorimotor anatomy of gait, balance, and falls.

Authors:  Colum D MacKinnon
Journal:  Handb Clin Neurol       Date:  2018

10.  Bilateral postsynaptic actions of pyramidal tract and reticulospinal neurons on feline erector spinae motoneurons.

Authors:  Mary Pauline Galea; Ingela Hammar; Elin Nilsson; Elzbieta Jankowska
Journal:  J Neurosci       Date:  2010-01-20       Impact factor: 6.167

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