Morphology and synaptic input of substance P receptor-immunoreactive interneurons in control and epileptic human hippocampus

被引:19
作者
Toth, K.
Wittner, L.
Urban, Z.
Doyle, W. K.
Buzsaki, G.
Shigemoto, R.
Freund, T. F.
Magloczky, Z.
机构
[1] Hungarian Acad Sci, Inst Expt Med, H-1450 Budapest, Hungary
[2] NYU, Sch Med, Dept Neurosurg, New York, NY 10016 USA
[3] Rutgers State Univ, Ctr Mol & Behav Neurosci, Newark, NJ 07102 USA
[4] Natl Inst Physiol Sci, Div Cerebral Struct, Okazaki, Aichi 4448585, Japan
关键词
GABA; SPR; temporal lobe epilepsy; synaptic reorganization; plasticity; inhibition;
D O I
10.1016/j.neuroscience.2006.09.039
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Substance P (SP) is known to be a peptide that facilitates epileptic activity of principal cells in the hippocampus. Paradoxically, in other models, it was found to be protective against seizures by activating substance P receptor (SPR)-expressing interneurons. Thus, these cells appear to play an important role in the generation and regulation of epileptic seizures. The number, distribution, morphological features and input characteristics of SPR-immunoreactive cells were analyzed in surgically removed hippocampi of 28 temporal lobe epileptic patients and eight control hippocampi in order to examine their changes in epileptic tissues. SPR is expressed in a subset of inhibitory cells in the control human hippocampus, they are multipolar interneurons with smooth dendrites, present in all hippocampal subfields. This cell population is considerably different from SPR-positive cells of the rat hippocampus. The CA1 (cornu Ammonis subfield 1) region was chosen for the detailed morphological analysis of the SPR-immunoreactive cells because of its extreme vulnerability in epilepsy. The presence of various neurochemical markers identifies functionally distinct interneuron types, such as those responsible for perisomatic, dendritic or interneuron-selective inhibition. We found considerable colocalization of SPR with calbindin but not with parvalbumin, calretinin, cholecystokinin and somatostatin, therefore we suppose that SPIR-positive cells participate mainly in dendritic inhibition. In the non-sclerotic CA1 region they are mainly preserved, whereas their number is decreased in the sclerotic cases. In the epileptic samples their morphology is considerably altered, they possessed more dendritic branches, which often became beaded. Analyses of synaptic coverage revealed that the ratio of symmetric synaptic input of SPR-immunoreactive cells has increased in epileptic samples. Our results suggest that SPR-positive cells are preserved while principal cells are present in the CA1 region, but show reactive changes in epilepsy including intense branching and growth of their dendritic arborization. (c) 2006 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:495 / 508
页数:14
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