Intrinsic optical imaging reveals regionally different manifestation of spreading depression in hippocampal and entorhinal structures in vitro

被引:26
作者
Buchheim, K
Weissinger, F
Siegmund, H
Holtkamp, M
Schuchmann, S
Meierkord, H
机构
[1] Humboldt Univ, Fak Med, Univ Klinikum Charite, Neurol Klin & Poliklin, D-10117 Berlin, Germany
[2] Humboldt Univ, Fak Med, Univ Klinikum Charite, Inst Physiol, D-10117 Berlin, Germany
关键词
spreading depression; intrinsic optical signal; spread pattern; spread velocity;
D O I
10.1006/exnr.2002.7893
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The spatiotemporal features of spreading depression (SD) were analyzed in vitro by using combined hippocampal-entorhinal cortex slices. SDs were induced by microinjection of 1 M KCl in the stratum radiatum of the CA1 region of the hippocampus. Measurements of extracellular field potentials, extracellular space (ECS) volume changes and intrinsic optical signal changes were combined to study SD features in different regions of the slice. Each SD was associated with a pronounced shrinkage of the extracellular space (ECS) volume and a decrease in light transmittance. The beginning of the optical signal change occurred simultaneously with the electrographic onset as measured with extracellular microelectrodes but outlasted the de shift for tens of seconds. The amplitude of the intrinsic optical signal change displayed marked regional variations with greatest changes of 12% in cortical regions. The signal amplitudes were considerably lower in hippocampal regions. The analysis of spread patterns revealed two types of waves: fully propagated waves spreading from CA1 all the way to the temporal neocortex and abortive waves that ceased earlier. The spread velocities displayed pronounced regional differences with highest velocities of 5.4 +/- 0.3 mm/min in the area CA3 of the hippocampal formation and lowest velocities of 2.7 +/- 0.1 mm/min in cortical regions. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:76 / 86
页数:11
相关论文
共 58 条
[1]   Use of intrinsic optical signals to monitor physiological changes in brain tissue slices [J].
Aitken, PG ;
Fayuk, D ;
Somjen, GG ;
Turner, DA .
METHODS, 1999, 18 (02) :91-103
[2]   Similar propagation of SD and hypoxic SD-like depolarization in rat hippocampus recorded optically and electrically [J].
Aitken, PG ;
Tombaugh, GC ;
Turner, DA ;
Somjen, GG .
JOURNAL OF NEUROPHYSIOLOGY, 1998, 80 (03) :1514-1521
[3]   Potential sources of intrinsic optical signals imaged in live brain slices [J].
Andrew, RD ;
Jarvis, CR ;
Obeidat, AS .
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1999, 18 (02) :185-+
[4]   Imaging NMDA- and kainate-induced intrinsic optical signals from the hippocampal slice [J].
Andrew, RD ;
Adams, JR ;
Polischuk, TM .
JOURNAL OF NEUROPHYSIOLOGY, 1996, 76 (04) :2707-2717
[5]   IMAGING CELL-VOLUME CHANGES AND NEURONAL EXCITATION IN THE HIPPOCAMPAL SLICE [J].
ANDREW, RD ;
MACVICAR, BA .
NEUROSCIENCE, 1994, 62 (02) :371-383
[6]   Evidence against volume regulation by cortical brain cells during acute osmotic stress [J].
Andrew, RD ;
Lobinowich, ME ;
Osehobo, EP .
EXPERIMENTAL NEUROLOGY, 1997, 143 (02) :300-312
[7]   ELECTROPHYSIOLOGICAL MEASUREMENTS OF VOLUME CHANGES IN LEECH NEUROPIL GLIAL-CELLS [J].
BALLANYI, K ;
GRAFE, P ;
SERVE, G ;
SCHLUE, WR .
GLIA, 1990, 3 (03) :151-158
[8]  
Basarsky TA, 1998, J NEUROSCI, V18, P7189
[9]   Analysis of MEG signals of spreading cortical depression with propagation constrained to a rectangular cortical strip II. Gyrencephalic swine model [J].
Bowyer, SM ;
Tepley, N ;
Papuashvili, N ;
Kato, S ;
Barkley, GL ;
Welch, KMA ;
Okada, YC .
BRAIN RESEARCH, 1999, 843 (1-2) :79-86
[10]   Intrinsic optical signal measurements reveal characteristic features during different forms of spontaneous neuronal hyperactivity associated with ECS shrinkage in vitro [J].
Buchheim, K ;
Schuchmann, S ;
Siegmund, H ;
Gabriel, HJ ;
Heinemann, U ;
Meierkord, H .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (06) :1877-1882