Literature DB >> 22542946

Extensive respiratory plasticity after cervical spinal cord injury in rats: axonal sprouting and rerouting of ventrolateral bulbospinal pathways.

Fannie Darlot1, Florence Cayetanot, Patrick Gauthier, Valéry Matarazzo, Anne Kastner.   

Abstract

Spinal cord injury (SCI) causes an interruption of descending motor and autonomic nervous tracts. However, a partial injury, and particularly a unilateral section, is generally followed by spontaneous locomotor and respiratory recovery. Although locomotor functional recovery has been correlated to spontaneous anatomical plasticity of the corticospinal tract, the remodeling of the bulbospinal tract that sustains respiratory improvement is unknown and has therefore been investigated here after chronic lateral cervical injury in rats (90 days post-lesion by comparison to 7 days post-lesion). We show that chronic lateral C2 SCI leads both to a decreased thickness of the ipsilateral ventrolateral funiculus at sus and sub-lesional levels and to an opposite effect on the contralateral side. At C1 level, the number of ventrolateral bulbospinal fibers, stained with anterograde tracer was reduced within the ipsilateral ventrolateral funiculi while collateral arborization toward the gray matter and growth associated protein-43 levels was increased. At C2 lesional level, fibers rerouting toward the gray matter were also identified for 5% of the axotomized axon terminals. Despite these chronic sprouting processes respiratory bulbospinal projections to ipsilateral phrenic nucleus remained poor (less than 10% compared to non-injured conditions). Retrograde labeling of projections onto the phrenic nucleus revealed, after chronic injury, an increased recruitment of C1 propriospinal interneurons which moreover received more contacts from bulbospinal collaterals. This chronic remodeling was correlated with chronic diaphragm recovery under conditions of respiratory stress. Thus, despite extensive axonal loss and absence of direct phrenic reinnervation by bulbospinal respiratory neurons, sprouting processes toward cervical propriospinal neurons may contribute to the observed partial respiratory recovery.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22542946     DOI: 10.1016/j.expneurol.2012.04.004

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  20 in total

1.  Decreased spinal synaptic inputs to phrenic motor neurons elicit localized inactivity-induced phrenic motor facilitation.

Authors:  K A Streeter; T L Baker-Herman
Journal:  Exp Neurol       Date:  2014-03-25       Impact factor: 5.330

2.  Use of quadrupedal step training to re-engage spinal interneuronal networks and improve locomotor function after spinal cord injury.

Authors:  Prithvi K Shah; Guillermo Garcia-Alias; Jaehoon Choe; Parag Gad; Yury Gerasimenko; Niranjala Tillakaratne; Hui Zhong; Roland R Roy; V Reggie Edgerton
Journal:  Brain       Date:  2013-10-07       Impact factor: 13.501

3.  Transplantation of bone marrow stromal cells enhances infiltration and survival of CNP and Schwann cells to promote axonal sprouting following complete transection of spinal cord in adult rats.

Authors:  Peng Ding; Zhiyong Yang; Weimin Wang; Jinkun Wang; Liping Xue
Journal:  Am J Transl Res       Date:  2014-05-15       Impact factor: 4.060

Review 4.  Enhancing neural activity to drive respiratory plasticity following cervical spinal cord injury.

Authors:  Kristiina M Hormigo; Lyandysha V Zholudeva; Victoria M Spruance; Vitaliy Marchenko; Marie-Pascale Cote; Stephane Vinit; Simon Giszter; Tatiana Bezdudnaya; Michael A Lane
Journal:  Exp Neurol       Date:  2016-08-28       Impact factor: 5.330

5.  Spontaneous respiratory plasticity following unilateral high cervical spinal cord injury in behaving rats.

Authors:  Tatiana Bezdudnaya; Kristiina M Hormigo; Vitaliy Marchenko; Michael A Lane
Journal:  Exp Neurol       Date:  2018-03-26       Impact factor: 5.330

6.  Integration of Transplanted Neural Precursors with the Injured Cervical Spinal Cord.

Authors:  Victoria M Spruance; Lyandysha V Zholudeva; Kristiina M Hormigo; Margo L Randelman; Tatiana Bezdudnaya; Vitaliy Marchenko; Michael A Lane
Journal:  J Neurotrauma       Date:  2018-04-24       Impact factor: 5.269

7.  Transplantation of Neural Progenitors and V2a Interneurons after Spinal Cord Injury.

Authors:  Lyandysha V Zholudeva; Nisha Iyer; Liang Qiang; Victoria M Spruance; Margo L Randelman; Nicholas W White; Tatiana Bezdudnaya; Itzhak Fischer; Shelly E Sakiyama-Elbert; Michael A Lane
Journal:  J Neurotrauma       Date:  2018-08-10       Impact factor: 5.269

8.  Supraspinal respiratory plasticity following acute cervical spinal cord injury.

Authors:  Tatiana Bezdudnaya; Vitaliy Marchenko; Lyandysha V Zholudeva; Victoria M Spruance; Michael A Lane
Journal:  Exp Neurol       Date:  2017-04-19       Impact factor: 5.330

9.  Spinal atypical protein kinase C activity is necessary to stabilize inactivity-induced phrenic motor facilitation.

Authors:  Kristi A Strey; Nicole L Nichols; Nathan A Baertsch; Oleg Broytman; Tracy L Baker-Herman
Journal:  J Neurosci       Date:  2012-11-14       Impact factor: 6.167

Review 10.  Respiration following spinal cord injury: evidence for human neuroplasticity.

Authors:  Daniel J Hoh; Lynne M Mercier; Shaunn P Hussey; Michael A Lane
Journal:  Respir Physiol Neurobiol       Date:  2013-07-26       Impact factor: 1.931

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