Tokimasa T
Jpn Heart J. 1981 Mar;22(2):227-37. doi: 10.1536/ihj.22.227.
The effect of 5-hydroxytryptamine (5-HT) on the isometric contraction, membrane potential, and membrane current of isolated bullfrog (Rama catesbeiana) atrium was investigated. 5-HT depressed the isometric contraction and this negative inotropism was atropine-resistant. 5-HT reduced both peak amplitude and duration of the action potential, but caused no detectable changes in the resting membrane potential and membrane input resistance. The final, or "secondary depolarization phase"1) in the rising phase of the action potential was found to be selectively depressed by 5-HT. These inhibitory effects on the action potential was also atropine-resistant. A single sucrose-gap voltage-clamp experiment revealed that 5-HT caused a reduction of the slow inward (Ca++/Na+) current. The membrane slope conductance near the resting membrane potential and the degree of activation of the of the time-dependent potassium current showed no detectable change in the presence of 5-HT. It was concluded on the basis of the present results that 5-HT directly controlled the action potential by selectively depressing the slow inward (Ca++/Na+) current. This may be responsible for the negative inotropic effect of 5-HT on bullfrog atrium.
研究了5-羟色胺(5-HT)对离体牛蛙(Rana catesbeiana)心房等长收缩、膜电位和膜电流的影响。5-HT抑制等长收缩,这种负性肌力作用对阿托品不敏感。5-HT降低了动作电位的峰值幅度和持续时间,但对静息膜电位和膜输入电阻没有可检测到的变化。发现动作电位上升相中的终末或“次级去极化期”1)被5-HT选择性抑制。这些对动作电位的抑制作用对阿托品也不敏感。单次蔗糖间隙电压钳实验表明,5-HT导致缓慢内向(Ca++/Na+)电流减小。在存在5-HT的情况下,静息膜电位附近的膜斜率电导和时间依赖性钾电流的激活程度没有可检测到的变化。根据目前的结果得出结论,5-HT通过选择性抑制缓慢内向(Ca++/Na+)电流直接控制动作电位。这可能是5-HT对牛蛙心房负性肌力作用的原因。