Encina J L, Hartung F, Tripathi O, Nawrath H
Pharmakologisches Institut der Universität Mainz, Federal Republic of Germany.
Naunyn Schmiedebergs Arch Pharmacol. 1988 Apr;337(4):435-9. doi: 10.1007/BF00169536.
The effects of forskolin on action potential configuration and on both uptake and efflux of 86Rb+ were studied in guinea-pig left atria. The action potential was prolonged by forskolin in the plateau range but shortened at the end of repolarization; maximal upstroke velocity and amplitude of slow response potentials were enhanced. In partially depolarized preparations, the resting potential was increased by forskolin; this effect was not prevented by atropine 1 mumol/l. Forskolin augmented the rate constant of 86Rb+ efflux in beating and in resting preparations. The uptake of 86Rb+ was enhanced by forskolin in resting preparations. It is concluded that forskolin stimulates the Na+,K+-pump and activates a background potassium conductance. Both effects may account for the shortening effect of the drug on the action potential and the increase in resting potential seen in partially depolarized preparations.
在豚鼠左心房中研究了福斯高林对动作电位形态以及86Rb+摄取和流出的影响。福斯高林使动作电位在平台期延长,但在复极化末期缩短;慢反应电位的最大上升速度和幅度增加。在部分去极化的标本中,福斯高林使静息电位升高;1 μmol/L阿托品不能阻止这种作用。福斯高林增加了跳动和静息标本中86Rb+的流出速率常数。在静息标本中,福斯高林增强了86Rb+的摄取。结论是福斯高林刺激Na+,K+-泵并激活背景钾电导。这两种作用可能解释了该药物对动作电位的缩短作用以及在部分去极化标本中观察到的静息电位增加。