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J Neurophysiol 89: 150-158, 2003; doi:10.1152/jn.00325.2002
0022-3077/03 $5.00
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J Neurophysiol (January 1, 2003). 10.1152/jn.00325.2002
Submitted on Submitted 2 May 2002; accepted in final form 13 September 2002

Reduction of Spontaneous Inhibitory Synaptic Activity in Experimental Heterotopic Gray Matter

Huan-Xin Chen1 and Steven N. Roper1,2

 1Department of Neurological Surgery and McKnight Brain Institute, University of Florida; and  2Malcolm Randall Veterans Affairs Medical Center, Gainesville, Florida 32610

Chen, Huan-Xin and Steven N. Roper. Reduction of Spontaneous Inhibitory Synaptic Activity in Experimental Heterotopic Gray Matter. J. Neurophysiol. 89: 150-158, 2003. Neuronal heterotopia has a strong association with epilepsy, but the mechanisms that underlie this relationship are largely unknown. We have utilized the in utero irradiated rat model to study circuit abnormalities in experimentally induced subcortical heterotopic gray matter. Spontaneous and miniature inhibitory (IPSCs) and excitatory (EPSCs) postsynaptic currents were recorded from visualized heterotopic pyramidal neurons in in vitro hemispheric slices and compared with control neocortical pyramidal neurons using the whole cell patch-clamp technique. The frequency of spontaneous and miniature IPSCs was significantly reduced in pyramidal neurons from heterotopic cortex. Amplitude and kinetics of IPSCs were not different between the two groups. Spontaneous and miniature EPSCs were not different between the two groups. Short-term synaptic plasticity of stimulus-evoked EPSCs showed depression in heterotopic neurons and facilitation in control pyramidal neurons. This study shows a selective impairment of the GABAergic circuitry in experimental heterotopic gray matter. We have reported similar findings in normotopic dysplastic cortex from this model. Taken together, these studies demonstrate a pervasive defect in inhibition throughout the cortex of irradiated rats with cortical dysplasia and neuronal heterotopia. This may have important implications regarding cortical development and function following in utero injuries.




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