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The Journal of Neuroscience, October 15, 1998, 18(20):8356-8368
Spine Loss and Other Persistent Alterations of Hippocampal
Pyramidal Cell Dendrites in a Model of Early-Onset Epilepsy
Minghui
Jiang,
Chong L.
Lee,
Karen L.
Smith, and
John
W.
Swann
The Cain Foundation Laboratories, Department of Pediatrics and
Division of Neuroscience, Baylor College of Medicine, Houston, Texas
77030
To explore the anatomical substrates for network hyperexcitability
in adult rats that become chronically epileptic after recurrent seizures in infancy, the dendritic and axonal arbors of biocytin-filled hippocampal pyramidal cells were reconstructed. On postnatal day 10, tetanus toxin was unilaterally injected into the hippocampus and
produced brief but recurrent seizures for 1 week. Later, hippocampal slices taken from these rats exhibited synchronized network bursts in
area CA3C. Both the apical and basilar dendritic arbors of CA3C pyramidal cells were markedly abnormal in these
epileptic rats. There was a considerable reduction in the density of
dendrite spines, although the extent of this loss could vary among
dendritic segments. Spine density on terminal segments of the basilar
and apical dendrites was reduced on average by 35 and 20%,
respectively. In addition, the diameters of these same dendritic
segments were markedly reduced. Dendritic spine loss has previously
been suggested to indicate a partial deafferentation of epileptic
neurons, but this interpretation is difficult to reconcile with the
critical role recurrent excitatory synaptic transmission plays in the
generation of synchronized network burst. In this study, axonal arbors
of CA3C pyramidal cells exhibited normal branching
patterns, branching complexity, and varicosity density. This suggests
that if deafferentation occurs, synapses other than recurrent
excitatory ones are lost. The morphological abnormalities reported here
would be expected to significantly alter electrical signaling within
dendrites that may contribute importantly to seizures and other
behavioral sequelae of early-onset epilepsy.
Key words:
hippocampus; dendrites; dendritic spines; axons; seizures; synapses
Copyright © 1998 Society for Neuroscience 0270-6474/98/18208356-13$05.00/0
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