𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Intrinsic excitability, synaptic potentials, and short-term plasticity in human epileptic neocortex

✍ Scribed by Uwe-Robert Koch; Ulrich Mußhoff; Heinz-Wolfgang Pannek; Alois Ebner; Peter Wolf; Erwin-Josef Speckmann; Rüdiger Köhling


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
490 KB
Volume
80
Category
Article
ISSN
0360-4012

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Although studies of epileptic human hippocampus suggest changes of synaptic and intrinsic excitability, few changes, save the appearance of spontaneous field/synaptic potentials, are known in epileptic neocortical tissue. However, invasive EEG and histological studies suggest that neocortical tissue, even in mesial temporal lobe epilepsy, can play an important role as an irritative zone or extrahippocampal focus. We hypothesized that intrinsic neuronal and synaptic excitability, as well as short‐term plasticity, are altered in neocortical areas, particularly with elevated K^+^ levels as occur during seizures. We analyzed neuronal firing properties, synaptic responses, and paired‐pulse plasticity in human neocortical slices from tissue resected during epilepsy surgery, both under normal and under pathological conditions, i.e., after elevating K^+^ (4/8 mM), with rat neocortical slices as controls. Neuronal firing properties were not different. We did find, however, alterations of synaptic responsiveness in epileptic tissue, i.e., an elevated network excitability with K^+^ elevations, and reduction of paired‐pulse depression. © 2005 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Age-related change in short-term synapti
✍ Xiaorong Ou; Galen Buckwalter; Thomas H. McNeill; John P. Walsh 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 194 KB 👁 2 views

Aging disrupts the expression of synaptic plasticity in many central nervous system (CNS) structures including the striatum. We found age differences in paired-pulse plasticity to persist at excitatory striatal synapses following block of gamma aminobutyric acid (GABA) A and GABA B receptors, a prop