Saikosaponin a Enhances Transient Inactivating Potassium Current in Rat Hippocampal CA1 Neurons

Author:

Xie Wei12,Yu Yun Hong12,Du Yong Ping3,Zhao Yun Yan4,Li Chang Zheng2,Yu Lin5,Duan Jian Hong6,Xing Jun Ling6

Affiliation:

1. Department of Traditional Chinese Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, China

2. School of Traditional Chinese Medicine, Southern Medical University, Guangzhou, Guangdong 510515, China

3. Department of Traditional Chinese Medicine, Xijing Hospital, Fourth Military Medical University, Xi’an, Shanxi 710032, China

4. Intensive Care Unit, Guang Zhou Municipal Hospital of Chinese Medicine, Guangzhou, Guangdong 510130, China

5. Department of Traditional Chinese Medicine, Guang Zhou Brain Hospital, Guangzhou, Guangdong 510170, China

6. Institute of Neuroscience, Fourth Military Medical University, Xi’an, Shanxi 710032, China

Abstract

Saikosaponin a (SSa), a main constituent of the Chinese herbBupleurum chinenseDC., has been demonstrated to have antiepileptic activity. Recent studies have shown that SSa could inhibit NMDA receptor current and persistent sodium current. However, the effects of SSa on potassium (K+) currents remain unclear. In this study, we tested the effect of SSa on 4AP-induced epileptiform discharges and K+currents in CA1 neurons of rat hippocampal slices. We found that SSa significantly inhibited epileptiform discharges frequency and duration in hippocampal CA1 neurons in the 4AP seizure model in a dose-dependent manner with anIC50of 0.7 μM. SSa effectively increased the amplitude ofITotalandIA, significantly negative-shifted the activation curve, and positive-shifted steady-state curve ofIA. However, SSa induced no significant changes in the amplitude and activation curve ofIK. In addition, SSa significantly increased the amplitude of 4AP-sensitive K+current, while there was no significant change in the amplitude of TEA-sensitive K+current. Together, our data indicate that SSa inhibits epileptiform discharges induced by 4AP in a dose-dependent manner and that SSa exerts selectively enhancing effects onIA. These increases inIAmay contribute to the anticonvulsant mechanisms of SSa.

Funder

National Natural Science Foundation of China

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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