School of Life Science and Biotechnology, Dalian University of Technology, Dalian, Liaoning 116024, PR China.
Toxicol In Vitro. 2011 Dec;25(8):1644-53. doi: 10.1016/j.tiv.2011.07.001. Epub 2011 Jul 21.
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 μM 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.
外向延迟整流钾通道和外向瞬间钾通道在维持海马神经元兴奋性方面具有多种重要作用。本研究探讨了两种蟾蜍毒素,蟾毒灵(RBG)和华蟾酥毒基(CBG)对大鼠海马神经元外向延迟整流钾电流(IK)和外向瞬间钾电流(IA)的影响。RBG 和 CBG 具有相似的结构,均从蟾蜍皮肤的毒腺中分离出来。RBG 抑制 IK 和 IA,而 CBG 抑制 IK,对 IA 无明显影响。此外,在 1 μM 浓度下,RBG 和 CBG 均可改变 IK 的一些通道动力学和门控特性,如稳态激活和失活曲线、开放概率和时间常数。这些发现表明,IK 可能是蟾毒灵的作用靶点,这可以解释蟾毒灵对中枢神经系统病理作用的机制。