首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >Effects of Resibufogenin and Cinobufagin on voltage-gated potassium channels in primary cultures of rat hippocampal neurons.
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Effects of Resibufogenin and Cinobufagin on voltage-gated potassium channels in primary cultures of rat hippocampal neurons.

机译:Resibufogenin和Cinobufagin对大鼠海马神经元原代培养物中电压门控钾通道的影响。

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摘要

Outward delayed rectifier potassium channel and outward transient potassium channel have multiple important roles in maintaining the excitability of hippocampal neurons. The present study investigated the effects of two bufadienolides, Resibufogenin (RBG) and Cinobufagin (CBG), on the outward delayed rectifier potassium current (IK) and outward transient potassium current (IA) in rat hippocampal neurons. RBG and CBG have similar structures and both were isolated from the venom gland of toad skin. RBG inhibited both IK and IA, whereas CBG inhibited IK without noticeable effect on IA. Moreover, at 1 muM concentration both RBG and CBG could alter some channel kinetics and gating properties of IK, such as steady-state activation and inactivation curves, open probability and time constants. These findings suggested that IK is probably a target of bufadienolides, which may explain the mechanisms of bufadienolides' pathological effects on central nervous system.
机译:向外延迟整流钾通道和向外瞬时钾通道在维持海马神经元的兴奋性中具有多个重要作用。本研究调查了两种异丁二烯内酯,异丁烯酸生成素(RBG)和奇诺蟾蜍精(CBG)对大鼠海马神经元向外延迟整流钾电流(IK)和向外瞬时钾电流(IA)的影响。 RBG和CBG具有相似的结构,并且都从蟾蜍皮的毒腺中分离出来。 RBG抑制IK和IA,而CBG抑制IK对IA无明显影响。此外,在1μM浓度下,RBG和CBG均可改变IK的某些通道动力学和门控特性,例如稳态激活和失活曲线,打开概率和时间常数。这些发现表明IK可能是布法非烯醇内酯的靶标,这可能解释了布法非烯醇内酯对中枢神经系统的病理作用机制。

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