Li Chun-Li, Yang Bao-Feng, Zhang Jing-Hai, Jiao Jun-Dong, Li Bao-Xin, Wu Chun-Fu
Department of Pharmacology, Shenyang Pharmaceutical University, Shenyang 110016, PR China.
Regul Pept. 2010 Sep 24;164(2-3):105-12. doi: 10.1016/j.regpep.2010.05.010. Epub 2010 Jun 8.
Previous studies have shown that the recombinant neurotoxic polypeptide BmK ANEP (ANEPIII) displayed good anti-neuroexcitation activity as demonstrated by pharmacological tests of the blockade of chemical-induced convulsive seizures. In order to search for further anticonvulsant mechanism of action of ANEPIII, the effects of ANEPIII on sodium channels were assessed using the whole-cell patch clamp recordings in primary cultures of rat hippocampal and cortical neurons. ANEPIII decreased the sodium currents in a voltage-dependent manner, which appeared as a shift of the current-voltage relation to positive potentials. The effect was reversible after washing. The concentration-responsiveness measured in hippocampal and cortical neurons revealed an IC(50) value of 124.6 nM and 192.7 nM, respectively. Furthermore, ANEPIII 1000 nM significantly shifted the activation curves of sodium current in hippocampal and cortical neurons to more positive potentials and the recovery from inactivation of sodium current was significantly slower. Voltage-dependent inactivation curves of sodium channels in hippocampal and cortical neurons did not change in the presence of 1000 nM ANEPIII. Thus, our results demonstrated that ANEPIII in submicromolar concentrations was a voltage-dependent, reversible blocker of sodium current in hippocampal and cortical neurons. It is concluded that these phenomena may explain, at least in part, the anti-neuroexciting properties of this peptide.
先前的研究表明,重组神经毒性多肽BmK ANEP(ANEPIII)表现出良好的抗神经兴奋活性,化学诱导惊厥发作的药理学试验证明了这一点。为了进一步探寻ANEPIII的抗惊厥作用机制,利用大鼠海马和皮质神经元原代培养物中的全细胞膜片钳记录,评估了ANEPIII对钠通道的影响。ANEPIII以电压依赖性方式降低钠电流,表现为电流-电压关系向正电位偏移。洗脱后该效应可逆。在海马和皮质神经元中测量的浓度-反应性显示,IC(50)值分别为124.6 nM和192.7 nM。此外,1000 nM的ANEPIII显著将海马和皮质神经元中钠电流的激活曲线向更正的电位移动,并且钠电流失活后的恢复明显减慢。在1000 nM ANEPIII存在的情况下,海马和皮质神经元中钠通道的电压依赖性失活曲线没有变化。因此,我们的结果表明,亚微摩尔浓度的ANEPIII是海马和皮质神经元中钠电流的电压依赖性、可逆性阻滞剂。得出的结论是,这些现象可能至少部分解释了该肽的抗神经兴奋特性。