Weng Xie-Chuan, Gai Xiao-Dan, Zheng Jian-Quan, Li Jin
Beijing Institute of Pharmacology and Toxicology, Beijing 100850, China.
Acta Pharmacol Sin. 2003 Aug;24(8):746-50.
To investigate the mechanism of agmatine by observing the effect of agmatine on the voltage-gated channels in rat hippocampal neurons.
The whole-cell patch recording technique was performed to record the voltage-gated potassium, sodium, and calcium currents in cultured rat hippocampus. Agmatine was applied directly to the single neuron using a pressure injector with microtubules.
Agmatine (500 micromol/L) had no significant effect on the voltage-gated potassium and sodium channels. Agmatine reversibly blocked the voltage-gated calcium channel and the blockade was enhanced with the increasing concentration of agmatine. The inhibitory rates were 21%+/-4%, 35%+/-6%, 49%+/-6%, 67%+/-4%, 69%+/-6%, 86%+/-8%, and 87%+/- 9%, at the concentration of 0.1, 0.5, 1.0, 5.0, 10.0, 50.0, and 100 micromol/L, respectively. IC50 was (1.2+/-0.4) micromol/L. Two-way ANOVA revealed that change of membrane potential displayed a significant interaction with the blockade by agmatine.
Agmatine reversibly blocked the voltage-gated calcium channel in rat hippocampal neurons in a concentration- and voltage-dependent way. Agmatine might perform its physiological and pharmacological effects partially by blocking the calcium channel.
通过观察胍丁胺对大鼠海马神经元电压门控通道的影响,探讨胍丁胺的作用机制。
采用全细胞膜片钳记录技术记录培养的大鼠海马神经元电压门控钾、钠和钙电流。使用带有微管的压力注射器将胍丁胺直接施加于单个神经元。
胍丁胺(500微摩尔/升)对电压门控钾通道和钠通道无显著影响。胍丁胺可逆性阻断电压门控钙通道,且随着胍丁胺浓度增加阻断作用增强。在0.1、0.5、1.0、5.0、10.0、50.0和100微摩尔/升浓度下,抑制率分别为21%±4%、35%±6%、49%±6%、67%±4%、69%±6%、86%±8%和87%±9%。半数抑制浓度(IC50)为(1.2±0.4)微摩尔/升。双向方差分析显示膜电位变化与胍丁胺的阻断作用存在显著交互作用。
胍丁胺以浓度和电压依赖的方式可逆性阻断大鼠海马神经元电压门控钙通道。胍丁胺可能部分通过阻断钙通道发挥其生理和药理作用。