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丹皮酚促进海马突触传递:Kv2.1 钾通道的作用。

Paeonol promotes hippocampal synaptic transmission: The role of the Kv2.1 potassium channel.

机构信息

School of Chinese Medicine, China Medical University, Taichung, Taiwan, ROC.

Graduate Institute of Pharmacology, College of Medicine, National Taiwan University, Taipei, Taiwan, ROC.

出版信息

Eur J Pharmacol. 2018 May 15;827:227-237. doi: 10.1016/j.ejphar.2018.03.020. Epub 2018 Mar 15.

Abstract

Paeonol is a major constituent of the Chinese herb Moutan cortex radices. Recent studies report that paeonol has neuroprotective effects and improves impaired learning and memory. However, its underlying mechanisms by which paeonol contributes to synaptic transmission remain unclear. In this study, we found that paeonol increased the frequency of miniature excitatory postsynaptic currents (mEPSCs) and spontaneous excitatory postsynaptic currents (sEPSCs), but had no effect on the amplitude in rat hippocampal CA1 neurons. Similarly, the acetylcholinesterase (AChE) inhibitor rivastigmine increased the frequency of mEPSCs, but had no effect upon amplitude in rat hippocampal neurons. Rivastigmine also inhibited the delayed outward K currents in rat hippocampal CA1 neurons, but had no effect in nucleus ambiguus (NA) neurons. The Kv2 blocker guangxitoxin-1E increased the frequency of both mEPSCs and sEPSCs of rat hippocampal CA1 neurons, without affecting their amplitude. Our results suggest that paeonol and rivastigmine enhance spontaneous presynaptic transmitter release, which may be associated with the inhibition of the hippocampal Kv2 current and with therapeutic potential in neurotransmitter deficits found in Alzheimer's disease (AD). Moreover, our data also show that paeonol protects against Aβ-induced impairment of long-term potentiation (LTP) in mouse hippocampal neurons. However, guangxitoxin-1E failed to potentiate the evoked field excitatory postsynaptic potentials (fEPSPs), LTP and Aβ-induced impairment of LTP. These results indicate that paeonol may has the potential to improve learning and memory in AD. Interestingly, this effect is not involved in the inhibition of the hippocampal Kv2 current.

摘要

丹皮酚是中国草药牡丹皮的主要成分。最近的研究报告称,丹皮酚具有神经保护作用,并改善受损的学习和记忆。然而,丹皮酚如何有助于突触传递的潜在机制尚不清楚。在这项研究中,我们发现丹皮酚增加了大鼠海马 CA1 神经元的微小兴奋性突触后电流 (mEPSC) 和自发性兴奋性突触后电流 (sEPSC) 的频率,但对幅度没有影响。同样,乙酰胆碱酯酶 (AChE) 抑制剂rivastigmine 增加了 mEPSC 的频率,但对大鼠海马神经元的幅度没有影响。rivastigmine 还抑制了大鼠海马 CA1 神经元的延迟外向 K 电流,但对疑核 (NA) 神经元没有影响。Kv2 阻断剂广息痛-1E 增加了大鼠海马 CA1 神经元的 mEPSC 和 sEPSC 的频率,而不影响其幅度。我们的结果表明,丹皮酚和 rivastigmine 增强了自发性突触前递质释放,这可能与抑制海马 Kv2 电流有关,并可能对阿尔茨海默病 (AD) 中发现的神经递质缺乏症具有治疗潜力。此外,我们的数据还表明,丹皮酚可防止 Aβ 诱导的小鼠海马神经元长时程增强 (LTP) 损伤。然而,广息痛-1E 未能增强诱发的场兴奋性突触后电位 (fEPSP)、LTP 和 Aβ 诱导的 LTP 损伤。这些结果表明,丹皮酚可能具有改善 AD 学习和记忆的潜力。有趣的是,这种作用不涉及抑制海马 Kv2 电流。

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