Failure of Repeated Electroconvulsive Shock Treatment on 5-HT4-Receptor-Mediated Depolarization Due To Protein Kinase A System in Young Rat Hippocampal CA1 Neurons

We previously demonstrated that repeated electroconvulsive shock (ECS) treatment enhanced serotonin (5-HT)1A- and 5-HT3-receptor-mediated responses in hippocampal CA1 pyramidal neurons. The electrophysiological studies were performed to elucidate the effects of ECS treatment on depolarization, which...

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Main Authors: Kumatoshi Ishihara (Author), Masashi Sasa (Author)
Format: Book
Published: Elsevier, 2004-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Kumatoshi Ishihara  |e author 
700 1 0 |a Masashi Sasa  |e author 
245 0 0 |a Failure of Repeated Electroconvulsive Shock Treatment on 5-HT4-Receptor-Mediated Depolarization Due To Protein Kinase A System in Young Rat Hippocampal CA1 Neurons 
260 |b Elsevier,   |c 2004-01-01T00:00:00Z. 
500 |a 1347-8613 
500 |a 10.1254/jphs.fp0030382 
520 |a We previously demonstrated that repeated electroconvulsive shock (ECS) treatment enhanced serotonin (5-HT)1A- and 5-HT3-receptor-mediated responses in hippocampal CA1 pyramidal neurons. The electrophysiological studies were performed to elucidate the effects of ECS treatment on depolarization, which was an additional response induced by 5-HT, and the second messenger system involved in this depolarization of hippocampal CA1 neurons. Bath application of 5-HT (100 μM) induced depolarization of the membrane potential in the presence of 5-HT1A-receptor antagonists. This depolarization was mimicked by 5-HT4-receptor agonists, RS 67506 (1 - 30 μM) and RS 67333 (0.1 - 30 μM), in a concentration-dependent manner. 5-HT- and RS 67333-induced depolarization was attenuated by concomitant application of RS 39604, a 5-HT4-receptor antagonist. H-89, a protein kinase A (PKA) inhibitor, inhibited 5-HT-, RS 67506-, and RS 67333-induced depolarizations, while forskolin (10 μM), an activator of adenylate cyclase, induced depolarization. Furthermore, RS 67333-induced depolarization was not significantly different between hippocampal slices prepared from rats administered ECS once a day for 14 days and those from sham-treated rats. These findings suggest that 5-HT4-receptor-mediated depolarization is caused via the cAMP-PKA system. In addition, repeated ECS-treatment did not modify 5-HT4-receptor functions in contrast to 5-HT1A- and 5-HT3-receptor functions. Keywords:: serotonin (5-HT), 5-HT4 receptor, depolarization, hippocampal CA1 region, electroconvulsive shock 
546 |a EN 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Journal of Pharmacological Sciences, Vol 95, Iss 3, Pp 329-334 (2004) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S1347861319324120 
787 0 |n https://doaj.org/toc/1347-8613 
856 4 1 |u https://doaj.org/article/ddb4d80b089840e19cc2be8d0487da6c  |z Connect to this object online.