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氨力农与豚鼠心房内源性腺苷的相互作用。

Interaction of amrinone with endogenous adenosine in guinea-pig atria.

作者信息

Dorigo P, Maragno I

出版信息

Br J Pharmacol. 1986 Apr;87(4):623-9. doi: 10.1111/j.1476-5381.1986.tb14578.x.

Abstract

In spontaneously beating atria from reserpine-treated guinea-pigs, amrinone (10 microM to 2 mM) induced a positive inotropic and chronotropic effect that was preceded by a transient reduction in contractile force and in frequency. Both the positive and negative effects were concentration-dependent. The inotropic action of amrinone was antagonized by low concentrations of 8-phenyltheophylline that compete with adenosine at R-receptors on plasma membrane without significantly influencing phosphodiesterase activity. Cumulative concentrations of amrinone (1 mM) antagonized the reduction of rate of contraction and amplitude induced by dipyridamole 1 microM in spontaneously beating atria and restored the maximum contractile effect reached in the absence of dipyridamole. In spontaneously beating preparations incubated in the presence of adenosine deaminase (1 u ml-1), amrinone lost its positive effects on the atria and only reduction of rate and contractile force was evident. Both effects were antagonized by scopolamine 1 mM thus indicating their cholinergic nature. Adenosine at 0.1 microM and 0.5 microM significantly inhibited the inotropic effect induced by amrinone (0.03 to 3 mM) and the concentration-effect curves of amrinone obtained in the absence and presence of adenosine clearly indicate a competitive antagonism between the two drugs. Thus the contractile activity of amrinone in spontaneously beating atria from reserpine-treated guinea-pigs originates from a displacement of adenosine from its R-receptor sites in the cardiac cell.

摘要

在利血平处理的豚鼠的自发搏动心房中,氨力农(10微摩尔至2毫摩尔)诱导了正性肌力和变时性效应,在此之前收缩力和频率有短暂降低。正负效应均呈浓度依赖性。低浓度的8-苯基茶碱可拮抗氨力农的正性肌力作用,该物质在质膜上的R受体处与腺苷竞争,而不显著影响磷酸二酯酶活性。氨力农(1毫摩尔)的累积浓度可拮抗1微摩尔双嘧达莫在自发搏动心房中诱导的收缩速率和幅度的降低,并恢复在无双嘧达莫时达到的最大收缩效应。在腺苷脱氨酶(1单位/毫升)存在下孵育的自发搏动制剂中,氨力农对心房失去其正性效应,仅明显降低速率和收缩力。这两种效应均被1毫摩尔东莨菪碱拮抗,因此表明它们具有胆碱能性质。0.1微摩尔和0.5微摩尔的腺苷显著抑制氨力农(0.03至3毫摩尔)诱导的正性肌力效应,在有无腺苷情况下获得的氨力农浓度-效应曲线清楚地表明两种药物之间存在竞争性拮抗作用。因此,氨力农在利血平处理的豚鼠自发搏动心房中的收缩活性源自腺苷从其在心肌细胞的R受体位点上被置换。

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