K+-evoked [3H]-norepinephrine release in human brain slices from epileptic and non-epileptic patients is differentially modulated by gabapentin and pinacidil

2006 ◽  
Vol 55 (2) ◽  
pp. 204-210 ◽  
Author(s):  
Thomas M. Freiman ◽  
Rainer Surges ◽  
Juraj Kukolja ◽  
Jan Heinemeyer ◽  
Maximilian Klar ◽  
...  
2010 ◽  
Vol 192 (1) ◽  
pp. 17-21 ◽  
Author(s):  
László Csiba ◽  
Szabolcs Farkas ◽  
József Kollár ◽  
Ervin Berényi ◽  
Katalin Nagy ◽  
...  

Author(s):  
Alastair J Kirby ◽  
José P Lavrador ◽  
Istvan Bodi ◽  
Francesco Vergani ◽  
Ranjeev Bhangoo ◽  
...  

Abstract Background Lower-grade gliomas may be indolent for many years before developing malignant behaviour. The reasons mechanisms underlying malignant progression remain unclear. Methods We collected blocks of live human brain tissue donated by people undergoing glioma resection. The tissue blocks extended through the peritumoral cortex and into the glioma. The living human brain tissue was cut into ex vivo brain slices and bathed in 5-aminolevulinic acid (5-ALA). High-grade glioma cells avidly take up 5-aminolevulinic acid (5-ALA) and accumulate high levels of the fluorescent metabolite, Protoporphyrin IX (PpIX). We exploited the PpIX fluorescence emitted by higher-grade glioma cells to investigate the earliest stages of malignant progression in lower-grade gliomas. Results We found sparsely-distributed ‘hot-spots’ of PpIX-positive cells in living lower-grade glioma tissue. Glioma cells and endothelial cells formed part of the PpIX hotspots. Glioma cells in PpIX hotspots were IDH1 mutant and expressed nestin suggesting they had acquired stem-like properties. Spatial analysis with 5-ALA conjugated quantum dots indicated that these glioma cells replicated adjacent to blood vessels. PpIX hotspots formed in the absence of angiogenesis. Conclusion Our data show that PpIX hotspots represent microdomains of cells with high-grade potential within lower-grade gliomas and identify locations where malignant progression could start.


1986 ◽  
Vol 61 (2) ◽  
pp. 71-73 ◽  
Author(s):  
Matthew W. Heller ◽  
Susan L. Stoddard
Keyword(s):  

2012 ◽  
Vol 287 (10) ◽  
pp. 7436-7445 ◽  
Author(s):  
Adriano Sebollela ◽  
Leo Freitas-Correa ◽  
Fabio F. Oliveira ◽  
Andrea C. Paula-Lima ◽  
Leonardo M. Saraiva ◽  
...  

2019 ◽  
Vol 21 (Supplement_4) ◽  
pp. iv16-iv16
Author(s):  
Alastair Kirby ◽  
Jose Pedro Lavrador ◽  
Christian Brogna ◽  
Francesco Vergani ◽  
Bassel Zebian ◽  
...  

Abstract Gliomas often present clinically with seizures. Tumour-associated seizures can be difficult to control with medication. A deeper understanding of the cellular mechanisms underlying tumour-associated seizures would provide a basis for developing new treatments. Here, we investigate epileptic discharges in peritumoral cortex using living human brain tissue donated by people having a craniotomy for glioma resection (REC approval, 18/SW/002). The brain tissue was cut into thin slices, which preserved the architecture of the glioma and the adjacent healthy brain. The brain slices were incubated in 5-aminolevulinic acid to make the glioma cells fluorescent. This enabled us to make electrophysiological recordings of brain activity across the boundary between glioma and brain. We recorded from brain slices of 5 participants with glioblastoma and 4 participants with oligodendroglioma (WHO grade II – III). Spontaneous “seizure-like” discharges were recorded in brain slices from 5/8 participants (3 GBM, 2 oligodendroglioma) who reported seizures and from one participant (GBM) who had not had any clinical seizures. Further analysis of the seizure-like discharges revealed that they could be subdivided into two distinct types based on the major frequencies in the discharge. We concluded that human brain slices from people with either a low-grade or a high-grade glioma can generate spontaneous seizure-like discharges. The living human brain tissue preparation gives us a platform to study the mechanisms of tumour-associated seizures and how abnormal neural activity affects glioma growth.


2001 ◽  
Vol 363 (5) ◽  
pp. 537-542 ◽  
Author(s):  
Thomas M. Freiman ◽  
Juraj Kukolja ◽  
Jan Heinemeyer ◽  
Klaus Eckhardt ◽  
Heike Aranda ◽  
...  

2003 ◽  
Vol 30 (12) ◽  
pp. 1630-1636 ◽  
Author(s):  
Philippe Levêque ◽  
Sandra Sanabria-Bohorquez ◽  
Anne Bol ◽  
Anne De Volder ◽  
Daniel Labar ◽  
...  

2007 ◽  
Vol 1142 ◽  
pp. 19-27 ◽  
Author(s):  
Toru Sasaki ◽  
Tadashi Nariai ◽  
Taketoshi Maehara ◽  
Katsushige Sato ◽  
Keiich Oda ◽  
...  

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