Literature DB >> 11284551

Short-Term and medium-term effects of spinal cord tract transections on soleus H-reflex in freely moving rats.

X Y Chen1, K C Feng-Chen, L Chen, D M Stark, J R Wolpaw.   

Abstract

Spinal cord function is normally influenced by descending activity from supraspinal structures. When injury removes or distorts this influence, function changes and spasticity and other disabling problems eventually appear. Understanding how descending activity affects spinal cord function could lead to new means for inducing, guiding, and assessing recovery after injury. In this study, we investigated the short-term and medium-term effects of spinal cord bilateral dorsal column (DC), unilateral (ipsilateral) lateral column (LC), bilateral dorsal column ascending tract (DA), or bilateral dorsal column corticospinal tract (CST) transection at vertebral level T8-T9 on the soleus H-reflex in freely moving rats. Data were collected continuously for 10-20 days before and for 20-155 days after bilateral DC (13 rats), DA (10 rats), CST (eight rats), or ipsilateral LC (seven rats) transection. Histological examination showed that transections were 98(+/- 3 SD)% complete for DC rats, 80(+/- 20)% complete for LC rats, 91(+/- 13 SD)% complete for DA rats, and 95(+/-13)% complete for CST rats. LC, CST, and DA transections produced an immediate (i.e., first-day) increase in H-reflex amplitude. LC transection also produced a small decrease in background activity in the first few posttransection days. Other than this small decrease, none of the transections produced evidence for the phenomenon of spinal shock. For all transections, all measures returned to or neared pretransection values within 2 weeks. DA and LC transections were associated with modest increase in H-reflex amplitude 1-3 months after transection. These medium-term effects must be taken into account when assessing transection effects on operant conditioning of the H-reflex. At the same time, the results are consistent with other evidence that, while H-reflex rate dependence and H-reflex operant conditioning are sensitive measures of spinal cord injury, the H-reflex itself is not.

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Year:  2001        PMID: 11284551     DOI: 10.1089/08977150151070973

Source DB:  PubMed          Journal:  J Neurotrauma        ISSN: 0897-7151            Impact factor:   5.269


  17 in total

1.  Locomotor impact of beneficial or nonbeneficial H-reflex conditioning after spinal cord injury.

Authors:  Yi Chen; Lu Chen; Rongliang Liu; Yu Wang; Xiang Yang Chen; Jonathan R Wolpaw
Journal:  J Neurophysiol       Date:  2013-12-26       Impact factor: 2.714

2.  Why New Spinal Cord Plasticity Does Not Disrupt Old Motor Behaviors.

Authors:  Yi Chen; Lu Chen; Yu Wang; Xiang Yang Chen; Jonathan R Wolpaw
Journal:  J Neurosci       Date:  2017-07-25       Impact factor: 6.167

3.  Persistent beneficial impact of H-reflex conditioning in spinal cord-injured rats.

Authors:  Yi Chen; Lu Chen; Yu Wang; Jonathan R Wolpaw; Xiang Yang Chen
Journal:  J Neurophysiol       Date:  2014-08-20       Impact factor: 2.714

4.  Up-regulation of 5-HT2 receptors is involved in the increased H-reflex amplitude after contusive spinal cord injury.

Authors:  Jae K Lee; Christopher S Johnson; Jean R Wrathall
Journal:  Exp Neurol       Date:  2006-10-23       Impact factor: 5.330

5.  Ablation of cerebellar nuclei prevents H-reflex down-conditioning in rats.

Authors:  Xiang Yang Chen; Jonathan R Wolpaw
Journal:  Learn Mem       Date:  2005 May-Jun       Impact factor: 2.460

6.  The inferior olive is essential for long-term maintenance of a simple motor skill.

Authors:  Xiang Yang Chen; Yu Wang; Yi Chen; Lu Chen; Jonathan R Wolpaw
Journal:  J Neurophysiol       Date:  2016-08-17       Impact factor: 2.714

7.  The cerebellum in maintenance of a motor skill: a hierarchy of brain and spinal cord plasticity underlies H-reflex conditioning.

Authors:  Jonathan R Wolpaw; Xiang Yang Chen
Journal:  Learn Mem       Date:  2006 Mar-Apr       Impact factor: 2.460

8.  The effects of passive exercise therapy initiated prior to or after the development of hyperreflexia following spinal transection.

Authors:  Charlotte C Yates; Amanda Charlesworth; Nancy B Reese; Robert D Skinner; Edgar Garcia-Rill
Journal:  Exp Neurol       Date:  2008-07-11       Impact factor: 5.330

9.  Ablation of the inferior olive prevents H-reflex down-conditioning in rats.

Authors:  Xiang Yang Chen; Yu Wang; Yi Chen; Lu Chen; Jonathan R Wolpaw
Journal:  J Neurophysiol       Date:  2016-01-20       Impact factor: 2.714

10.  Modafinil normalized hyperreflexia after spinal transection in adult rats.

Authors:  C C Yates; A Charlesworth; N B Reese; K Ishida; R D Skinner; E Garcia-Rill
Journal:  Spinal Cord       Date:  2008-12-16       Impact factor: 2.772

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