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Neuropharmacology. 2014 Mar;78:55-62. doi: 10.1016/j.neuropharm.2013.04.058. Epub 2013 May 29.

Homeostatic synaptic plasticity in developing spinal networks driven by excitatory GABAergic currents.

Author information

1
Emory University, School of Medicine, 615 Michael Street, Rm 601, Physiology Department, Atlanta, GA 30322, United States. Electronic address: pwenner@emory.edu.

Abstract

Homeostatic plasticity refers to mechanisms that the cell or network engage in order to homeostatically maintain a preset level of activity. These mechanisms include compensatory changes in cellular excitability, excitatory and inhibitory synaptic strength and are typically studied at a developmental stage when GABA or glycine is inhibitory. Here we focus on the expression of homeostatic plasticity in the chick embryo spinal cord at a stage when GABA is excitatory. When spinal activity is perturbed in the living embryo there are compensatory changes in postsynaptic AMPA receptors and in the driving force for GABAergic currents. These changes are triggered by reduced GABAA receptor signaling, which appears to be part of the sensing machinery for triggering homeostatic plasticity. We compare and contrast these findings to homeostatic plasticity expressed in spinal systems at different stages of development, and to the developing retina at a stage when GABA is depolarizing. This article is part of the Special Issue entitled 'Homeostatic Synaptic Plasticity'.

KEYWORDS:

Chick embryo; Motoneuron; Network activity

PMID:
23727439
PMCID:
PMC3796029
DOI:
10.1016/j.neuropharm.2013.04.058
[Indexed for MEDLINE]
Free PMC Article

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