Literature DB >> 22037910

Manipulations of spinal cord excitability evoke developmentally-dependent compensatory changes in the lamprey spinal cord.

Ria Mishaal Cooke1, Sophie Luco, David Parker.   

Abstract

We have examined homeostatic or compensatory plasticity evoked by tonic changes in spinal cord excitability in the lamprey, a model system for investigating spinal cord function. In larval animals, reducing excitability by incubating in tetrodotoxin or the glutamate receptor antagonists CNQX or CNQX/AP5 for 20-48 h resulted in a diverse set of cellular and synaptic changes that together were consistent with an increase in spinal cord excitability. Similar changes occurred to a tonic increase in excitation evoked by incubating in high potassium physiological solution (i.e. responses were unidirectional). We also examined developmental influences on these effects. In animals developing from the larval to adult form effects were reduced or absent, suggesting that at this stage the spinal cord was more tolerant of changes in activity levels. Responses had returned in adult animals, but they were now bi-directional (i.e. opposite effects were evoked by an increase or decrease in excitability). The spinal cord can thus monitor and adapt cellular and synaptic properties to tonic changes in excitability levels. This should be considered in analyses of spinal cord plasticity and injury.

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Year:  2011        PMID: 22037910     DOI: 10.1007/s00359-011-0683-0

Source DB:  PubMed          Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol        ISSN: 0340-7594            Impact factor:   1.836


  61 in total

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2.  Modelling of intersegmental coordination in the lamprey central pattern generator for locomotion.

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Review 3.  Neurobiology of lampreys.

Authors:  C M Rovainen
Journal:  Physiol Rev       Date:  1979-10       Impact factor: 37.312

Review 4.  Homeostatic signaling: the positive side of negative feedback.

Authors:  Gina Turrigiano
Journal:  Curr Opin Neurobiol       Date:  2007-04-23       Impact factor: 6.627

5.  Compensatory changes in cellular excitability, not synaptic scaling, contribute to homeostatic recovery of embryonic network activity.

Authors:  Jennifer C Wilhelm; Mark M Rich; Peter Wenner
Journal:  Proc Natl Acad Sci U S A       Date:  2009-04-03       Impact factor: 11.205

6.  Transition to endogenous bursting after long-term decentralization requires De novo transcription in a critical time window.

Authors:  M Thoby-Brisson; J Simmers
Journal:  J Neurophysiol       Date:  2000-07       Impact factor: 2.714

7.  Activity-dependent feedforward inhibition modulates synaptic transmission in a spinal locomotor network.

Authors:  David Parker
Journal:  J Neurosci       Date:  2003-12-03       Impact factor: 6.167

8.  Substance P modulates NMDA responses and causes long-term protein synthesis-dependent modulation of the lamprey locomotor network.

Authors:  D Parker; W Zhang; S Grillner
Journal:  J Neurosci       Date:  1998-06-15       Impact factor: 6.167

9.  Identification of excitatory interneurons contributing to generation of locomotion in lamprey: structure, pharmacology, and function.

Authors:  J T Buchanan; S Grillner; S Cullheim; M Risling
Journal:  J Neurophysiol       Date:  1989-07       Impact factor: 2.714

10.  Timing of neuronal and glial ultrastructure disruption during brain slice preparation and recovery in vitro.

Authors:  John C Fiala; Sergei A Kirov; Marcia D Feinberg; Lara J Petrak; Priya George; C Alex Goddard; Kristen M Harris
Journal:  J Comp Neurol       Date:  2003-10-06       Impact factor: 3.215

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  2 in total

1.  Changes in functional properties and 5-HT modulation above and below a spinal transection in lamprey.

Authors:  Matthew I Becker; David Parker
Journal:  Front Neural Circuits       Date:  2015-01-20       Impact factor: 3.492

2.  Rapid activity-dependent modulation of the intrinsic excitability through up-regulation of KCNQ/Kv7 channel function in neonatal spinal motoneurons.

Authors:  Joseph Lombardo; Jianli Sun; Melissa A Harrington
Journal:  PLoS One       Date:  2018-03-26       Impact factor: 3.240

  2 in total

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