TY - JOUR
T1 - Cellular pathology of amygdala neurons in human temporal lobe epilepsy
AU - Aliashkevich, Ales F.
AU - Yilmazer-Hanke, Deniz
AU - Van Roost, Dirk
AU - Mundhenk, Björn
AU - Schramm, Johannes
AU - Blümcke, Ingmar
N1 - Funding Information:
Acknowledgments This work was supported by the Deutsche Forschungsgemeinschaft (Sonderforschungsbereich TR3, TP B2) and by a center grant from the University of Bonn Medical Center (BONFOR). We thank S. Normann for her technical assistance.
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2003/8/2
Y1 - 2003/8/2
N2 - The amygdala complex substantially contributes to the generation and propagation of focal seizures in patients suffering from temporal lobe epilepsy (TLE). A cellular substrate for increased excitability in the human amygdala, however, remains to be identified. Here, we analyzed the three-dimensional morphology of 264 neurons from different subregions of the amygdaloid complex obtained from 17 "en bloc" resected surgical specimens using intracellular Lucifer Yellow (LY) injection and confocal laser scanning microscopy. Autopsy samples from unaffected individuals (n=3, 20 neurons) served as controls. We have identified spine-laden, spine-sparse and aspinous cells in the lateral, basal, accessory basal and granular nuclei. Semiquantitative analysis points to significant changes in neuronal soma size, number of dendrites and spine densities in specimens from epilepsy patients compared to controls. Neuronal somata in the epilepsy group were smaller compared to controls (P
AB - The amygdala complex substantially contributes to the generation and propagation of focal seizures in patients suffering from temporal lobe epilepsy (TLE). A cellular substrate for increased excitability in the human amygdala, however, remains to be identified. Here, we analyzed the three-dimensional morphology of 264 neurons from different subregions of the amygdaloid complex obtained from 17 "en bloc" resected surgical specimens using intracellular Lucifer Yellow (LY) injection and confocal laser scanning microscopy. Autopsy samples from unaffected individuals (n=3, 20 neurons) served as controls. We have identified spine-laden, spine-sparse and aspinous cells in the lateral, basal, accessory basal and granular nuclei. Semiquantitative analysis points to significant changes in neuronal soma size, number of dendrites and spine densities in specimens from epilepsy patients compared to controls. Neuronal somata in the epilepsy group were smaller compared to controls (P
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U2 - 10.1007/s00401-003-0707-0
DO - 10.1007/s00401-003-0707-0
M3 - Article
C2 - 12684832
AN - SCOPUS:0037593258
VL - 106
SP - 99
EP - 106
JO - Acta Neuropathologica
JF - Acta Neuropathologica
SN - 0001-6322
IS - 2
ER -