scholarly journals Voltage Imaging Reveals the CA1 Region at the CA2 Border as a Focus for Epileptiform Discharges and Long-Term Potentiation in Hippocampal Slices

2007 ◽  
Vol 98 (3) ◽  
pp. 1309-1322 ◽  
Author(s):  
Payne Y. Chang ◽  
Portia E. Taylor ◽  
Meyer B. Jackson

Voltage-sensitive-dye imaging was used to study the initiation and propagation of epileptiform activity in transverse hippocampal slices. A portion of the slices tested generated epileptiform discharges in response to electrical shocks under normal physiological conditions. The fraction of slices showing epileptiform responses increased from 44 to 86% when bathing [K+] increased from 3.2 to 4 mM. Regardless of stimulation site in the dentate gyrus and hippocampus, discharges generally initiated in the CA3 region. After onset, discharges abruptly appeared in the CA1 region, right at the CA2 border. This spread from the CA3 region to the CA1 region was saltatory, occurring before detectable activity in the intervening CA2 and CA3 regions. Discharges did eventually propagate smoothly through the intervening CA3 region into the CA2 region, but on a slower timescale. The surge in the CA1 region did not spread back into the CA2 region, but spread through the CA1 region toward the subiculum. Tetanic stimulation, theta bursts, and GABAA receptor antagonists failed to alter this characteristic pattern, but did reduce the latency of discharge onset. The part of the CA1 region at the CA2 border, where epileptic responses emerged with relatively short latency, also expressed stronger long-term potentiation (LTP) than the rest of the CA1 region. The CA2 region, where discharges had long latencies and low amplitudes, expressed weaker LTP. Thus the CA1 region at the CA2 border has unique properties, which make this part of the hippocampus an important locus for both epileptiform activity and plasticity.

1990 ◽  
Vol 68 (3) ◽  
pp. 413-418 ◽  
Author(s):  
Takeshi Fujii ◽  
Yasushi Kuraishi ◽  
Toshikazu Okada ◽  
Masamichi Satoh

We made use of the [3H]phorbol 12,13-dibutyrate binding assay to investigate the effects of bifemelane on the subcellular distribution of protein kinase C in the CA3 and CA1 regions of guinea-pig hippocampal slices. Bifemelane, a drug that augments the long-term potentiation in the CA3 region, significantly induced the translocation of [3H]phorbol 12,13-dibutyrate binding activity from the cytosol to the membrane in a dose-dependent manner (10−8 to 10−6 M) and with no effects on total binding activity in the CA3 region. Bifemelane, at a concentration of 10−6 M, was without effect on the subcellular distribution of [3H]phorbol 12,13-dibutyrate binding activity in the CA1 region. These observations suggest that bifemelane acts directly on the hippocampus to induce translocation of protein kinase C in the CA3 region. Such an effect may be associated with the bifemelane-induced augmentation of the long-term potentiation in this region of the brain.Key words: bifemelane, protein kinase C, hippocampal slice, translocation, CA3.


2003 ◽  
Vol 965 (1-2) ◽  
pp. 108-113 ◽  
Author(s):  
Fereshteh Salmanzadeh ◽  
Yaghoub Fathollahi ◽  
Saeed Semnanian ◽  
Mahshid Shafizadeh

1990 ◽  
Vol 181 (3) ◽  
pp. 323-326 ◽  
Author(s):  
Hiroshi Katsuki ◽  
Satoru Nakai ◽  
Yoshikatsu Hirai ◽  
Ken-ichi Akaji ◽  
Yoshiaki Kiso ◽  
...  

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