Krstew E, McPherson G A, Malta E, Molenaar P, Raper C
Br J Pharmacol. 1984 Jun;82(2):501-8. doi: 10.1111/j.1476-5381.1984.tb10786.x.
Ro 03-7894 (0.6 mM) produced a non-parallel shift to the right of dose-response curves to (-)-isoprenaline in K+ depolarized uterine preparations from the guinea-pig. The displacement of the curves was readily reversed by washing. A rightward shift of similar magnitude was also produced by Ro 03-7894 in transmurally stimulated ileal preparations. The relaxant effects of fenoterol in carbachol-contracted guinea-pig tracheal preparations (in the presence of 2 microM atenolol) were not altered by 0.6 mM Ro 03-7894. In the three tissues there was no evidence of a reduction in the maximal inhibitory response to the agonists. In uterine and tracheal preparations, Ro 03-7894 (0.6 mM) depressed contractile responses to exogenous calcium. The depression of responses was enhanced after washout of Ro 03-7894 for 80 min. Contractile responses of ileal preparations to transmural stimulation were also depressed by Ro 03-7894. Concentration-effect curves for the positive inotropic effects of (-)-isoprenaline in guinea-pig left atrial preparations were markedly shifted to the right and the maximum response depressed by 0.6 mM Ro 03-7894. Although the rightward shift of the curves was fully reversed during the 120 min washout period, the maximal responses remained depressed. In similar experiments, Ro 03-7894 produced a washout-resistant depression of inotropic responses to histamine and calcium. The results of radioligand binding studies in left atria using (-)-[125I]-iodocyanopindolol indicated that, when compared to the untreated atria, there was no reduction in the maximal density of binding sites 120 min after washout of 0.6 mM Ro 03-7894. 5 On the basis of the present results it is concluded that Ro 03-7894 induces a non-specific depressant effect on smooth and cardiac muscle preparations during exposure to the drug. This depressant effect persists following washout of the drug. There is no evidence for an irreversible effect of Ro 03-7894 at beta-adrenoceptor sites.
Ro 03-7894(0.6 mM)使豚鼠子宫制备物中K⁺去极化后对(-)-异丙肾上腺素的剂量反应曲线向右非平行移动。经冲洗后,曲线的位移很容易逆转。Ro 03-7894在经透壁刺激的回肠制备物中也产生了类似幅度的右移。在豚鼠气管制备物中,卡巴胆碱收缩状态下(存在2 microM阿替洛尔),非诺特罗的舒张作用不受0.6 mM Ro 03-7894的影响。在这三种组织中,没有证据表明对激动剂的最大抑制反应降低。在子宫和气管制备物中,Ro 03-7894(0.6 mM)抑制对外源性钙的收缩反应。在冲洗Ro 03-7894 80分钟后,反应的抑制作用增强。Ro 03-7894也抑制回肠制备物对透壁刺激的收缩反应。在豚鼠左心房制备物中,(-)-异丙肾上腺素的正性肌力作用的浓度-效应曲线明显右移,0.6 mM Ro 03-7894使最大反应降低。尽管在120分钟的冲洗期内曲线的右移完全逆转,但最大反应仍降低。在类似实验中,Ro 03-7894对组胺和钙的肌力反应产生了冲洗后仍持续存在的抑制作用。使用(-)-[¹²⁵I]-碘氰吲哚洛尔对左心房进行放射性配体结合研究的结果表明,与未处理的心房相比,在冲洗0.6 mM Ro 03-7894 120分钟后,结合位点的最大密度没有降低。基于目前的结果得出结论,Ro 03-7894在药物暴露期间对平滑肌和心肌制备物诱导非特异性抑制作用。药物冲洗后,这种抑制作用仍然存在。没有证据表明Ro 03-7894在β-肾上腺素受体位点有不可逆作用。