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麦冬皂苷 D 对急性分离的大鼠气管旁神经元钾离子电导的激活作用。

Activation of potassium conductance by ophiopogonin-D in acutely dissociated rat paratracheal neurones.

作者信息

Ishibashi H, Mochidome T, Okai J, Ichiki H, Shimada H, Takahama K

机构信息

Department of Hygienic Chemistry, Faculty of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-Honmachi, Kumamoto 862-0973, Japan.

出版信息

Br J Pharmacol. 2001 Jan;132(2):461-6. doi: 10.1038/sj.bjp.0703818.

Abstract
  1. The effect of ophiopogonin-D (OP-D), a steroidal glycoside and an active component of Bakumondo-to, a Chinese herbal antitussive, on neurones acutely dissociated from paratracheal ganglia of 2-week-old Wistar rats was investigated using the nystatin-perforated patch recording configuration. 2. Under current-clamp conditions, OP-D (10 microM) hyperpolarized the paratracheal neurones from a resting membrane potential of -65.7 to -73.5 mV. 3. At the concentration of 1 microM and above, OP-D concentration-dependently activated an outward current accompanied by an increase in the membrane conductance under voltage-clamp conditions at a holding potential of -40 mV. 4. The reversal potential of the OP-D-induced current (I(OP-D)) was -79.4 mV, which is close to the K(+) equilibrium potential of -86.4 mV. The changes in the reversal potential for a 10 fold change in extracellular K(+) concentration was 53.1 mV, indicating that the current was carried by K(+). 5. The I(OP-D) was blocked by an extracellular application of 1 mM Ba2+ by 59.0%, but other K(+) channel blockers, including 4-aminopyridine (3 mM), apamin (1 microM), charybdotoxin (0.3 microM), glibenclamide (1 microM), tolbutamide (0.3 mM) and tetraethylammonium (10 mM), did not inhibit the I(OP-D). 6. OP-D also inhibited the ACh- and bradykinin-induced depolarizing responses which were accompanied with firing of action potentials. 7. The results suggest that OP-D may be of benefit in reducing the excitability of airway parasympathetic ganglion neurones and consequently cholinergic control of airway function and further, that the hyperpolarizing effect of OP-D on paratracheal neurones via an activation of K(+) channels might explain a part of mechanisms of the antitussive action of the agent.
摘要
  1. 麦冬皂苷-D(OP-D)是一种甾体糖苷,也是中药止咳剂八味地黄丸的活性成分,本研究采用制霉菌素穿孔膜片钳记录技术,研究其对2周龄Wistar大鼠气管旁神经节急性分离神经元的作用。2. 在电流钳条件下,OP-D(10μM)使气管旁神经元的静息膜电位从-65.7mV超极化至-73.5mV。3. 在-40mV的钳制电位下,电压钳条件下,浓度为1μM及以上时,OP-D浓度依赖性地激活外向电流,并伴有膜电导增加。4. OP-D诱导电流(I(OP-D))的反转电位为-79.4mV,接近K(+)平衡电位-86.4mV。细胞外K(+)浓度变化10倍时,反转电位变化53.1mV,表明该电流由K(+)携带。5. 细胞外应用1mM Ba2+可使I(OP-D)阻断59.0%,但其他K(+)通道阻滞剂,包括4-氨基吡啶(3mM)、蜂毒明肽(1μM)、大蝎毒素(0.3μM)、格列本脲(1μM)、甲苯磺丁脲(0.3mM)和四乙铵(10mM),均不抑制I(OP-D)。6. OP-D还抑制ACh和缓激肽诱导的去极化反应,这些反应伴有动作电位发放。7. 结果表明,OP-D可能有助于降低气道副交感神经节神经元的兴奋性,从而减少气道功能的胆碱能控制;此外,OP-D通过激活K(+)通道对气管旁神经元的超极化作用可能解释了该药物止咳作用的部分机制。

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本文引用的文献

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