Literature DB >> 31769033

Somatosensory corticospinal tract axons sprout within the cervical cord following a dorsal root/dorsal column spinal injury in the rat.

Margaret M McCann1,2, Karen M Fisher1, Jamie Ahloy-Dallaire1,3, Corinna Darian-Smith1.   

Abstract

The corticospinal tract (CST) is the major descending pathway controlling voluntary hand function in primates, and though less dominant, it mediates voluntary paw movements in rats. As with primates, the CST in rats originates from multiple (albeit fewer) cortical sites, and functionally different motor and somatosensory subcomponents terminate in different regions of the spinal gray matter. We recently reported in monkeys that following a combined cervical dorsal root/dorsal column lesion (DRL/DCL), both motor and S1 CSTs sprout well beyond their normal terminal range. The S1 CST sprouting response is particularly dramatic, indicating an important, if poorly understood, somatosensory role in the recovery process. As rats are used extensively to model spinal cord injury, we asked if the S1 CST response is conserved in rodents. Rats were divided into sham controls, and two groups surviving post-lesion for ~6 and 10 weeks. A DRL/DCL was made to partially deafferent one paw. Behavioral testing showed a post-lesion deficit and recovery over several weeks. Three weeks prior to ending the experiment, S1 cortex was mapped electrophysiologically, for tracer injection placement to determine S1 CST termination patterns within the cord. Synaptogenesis was also assessed for labeled S1 CST terminals within the dorsal horn. Our findings show that the affected S1 CST sprouts well beyond its normal range in response to a DRL/DCL, much as it does in macaque monkeys. This, along with evidence for increased synaptogenesis post-lesion, indicates that CST terminal sprouting following a central sensory lesion, is a robust and conserved response.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  RRID: AB_10983675; RRID: AB_2298772; RRID: AB_2338046; RRID: AB_2535804; RRID: AB_2564643; corticospinal tract; dorsal column; dorsal rhizotomy; primary afferent lesion; rats; somatosensory; spinal cord injury

Year:  2019        PMID: 31769033      PMCID: PMC7102935          DOI: 10.1002/cne.24826

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


  65 in total

1.  Commissural interneurons with input from group I and II muscle afferents in feline lumbar segments: neurotransmitters, projections and target cells.

Authors:  E Jankowska; B A Bannatyne; K Stecina; I Hammar; A Cabaj; D J Maxwell
Journal:  J Physiol       Date:  2008-12-01       Impact factor: 5.182

2.  Corticospinal projection patterns following unilateral section of the cervical spinal cord in the newborn and juvenile macaque monkey.

Authors:  M P Galea; I Darian-Smith
Journal:  J Comp Neurol       Date:  1997-05-12       Impact factor: 3.215

3.  Contribution of propriospinal neurons to recovery of hand dexterity after corticospinal tract lesions in monkeys.

Authors:  Takamichi Tohyama; Masaharu Kinoshita; Kenta Kobayashi; Kaoru Isa; Dai Watanabe; Kazuto Kobayashi; Meigen Liu; Tadashi Isa
Journal:  Proc Natl Acad Sci U S A       Date:  2017-01-03       Impact factor: 11.205

4.  Organization of corticospinal neurons in the monkey.

Authors:  E A Murray; J D Coulter
Journal:  J Comp Neurol       Date:  1981-01-10       Impact factor: 3.215

5.  Targeting recovery: priorities of the spinal cord-injured population.

Authors:  Kim D Anderson
Journal:  J Neurotrauma       Date:  2004-10       Impact factor: 5.269

6.  Macaque red nucleus: origins of spinal and olivary projections and terminations of cortical inputs.

Authors:  K Burman; C Darian-Smith; I Darian-Smith
Journal:  J Comp Neurol       Date:  2000-07-24       Impact factor: 3.215

7.  Corticospinal sprouting differs according to spinal injury location and cortical origin in macaque monkeys.

Authors:  Corinna Darian-Smith; Alayna Lilak; Joseph Garner; Karen-Amanda Irvine
Journal:  J Neurosci       Date:  2014-09-10       Impact factor: 6.167

Review 8.  Cortical and subcortical plasticity in the brains of humans, primates, and rats after damage to sensory afferents in the dorsal columns of the spinal cord.

Authors:  Jon H Kaas; Hui-Xin Qi; Mark J Burish; Omar A Gharbawie; Stephen M Onifer; James M Massey
Journal:  Exp Neurol       Date:  2007-07-06       Impact factor: 5.330

9.  Reorganization of the Primate Dorsal Horn in Response to a Deafferentation Lesion Affecting Hand Function.

Authors:  Karen M Fisher; Joseph P Garner; Corinna Darian-Smith
Journal:  J Neurosci       Date:  2020-01-20       Impact factor: 6.167

Review 10.  Spinal Control of Locomotion: Individual Neurons, Their Circuits and Functions.

Authors:  Marie-Pascale Côté; Lynda M Murray; Maria Knikou
Journal:  Front Physiol       Date:  2018-06-25       Impact factor: 4.566

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  2 in total

1.  Behavioral recovery after a spinal deafferentation injury in monkeys does not correlate with extent of corticospinal sprouting.

Authors:  Matthew Crowley; Alayna Lilak; Joseph P Garner; Corinna Darian-Smith
Journal:  Behav Brain Res       Date:  2021-08-25       Impact factor: 3.332

2.  Quantitative electrophysiological assessments as predictive markers of lower limb motor recovery after spinal cord injury: a pilot study with an adaptive trial design.

Authors:  Yin Nan Huang; El-Mehdi Meftah; Charlotte H Pion; Jean-Marc Mac-Thiong; Julien Cohen-Adad; Dorothy Barthélemy
Journal:  Spinal Cord Ser Cases       Date:  2022-02-24
  2 in total

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