Bongrani S, Razzetti R, Papotti M, Pastore F, Bergamaschi M
Pharmacological Department, Chiesi Farmaceutici S.p.A., Parma, Italy.
Arzneimittelforschung. 1990 Feb;40(2 Pt 1):169-74.
The cardiac effects of bamifylline (Bamifix), an alkylxanthine derivative, were evaluated on in vivo and in vitro cardiac preparations and compared with those of theophylline and enprofylline. In isolated rat and guinea-pig right atria bamifylline, in contrast to the other xanthines, left the rate of contraction unchanged or reduced it. In isolated rat and guinea-pig left atria the compound induced only slight inotropic effects showing an intrinsic activity significantly lower than that of theophylline and enprofylline. In isolated rabbit papillary muscles bamifylline administration was without effect up to 10(-3) mol/l and decreased the contractile force at a higher concentration, while theophylline dose-dependently increased inotropism. Also in anaesthetized rabbits intravenous administration of bamifylline produced negative chronotropic and dromotropic effects that were associated, at the highest dose, with a reduction of myocardial contractility. Theophylline and enprofylline, at the same equimolar doses, induced positive chronotropic and inotropic effects. The results show that bamifylline is devoid of cardiostimulant effects in respect to other xanthine derivatives. Moreover, they suggest that bamifylline acts on cardiac muscle by a mechanism, probably linked to the Ca+(+)-movements across the cardiac membrane, able to outweigh the effects due to its antiphosphodiesterase activity.
对烷基黄嘌呤衍生物巴米茶碱(Bamifix)的心脏效应进行了体内和体外心脏制剂评估,并与茶碱和恩丙茶碱进行了比较。与其他黄嘌呤不同,在离体大鼠和豚鼠右心房中,巴米茶碱使收缩速率保持不变或降低。在离体大鼠和豚鼠左心房中,该化合物仅产生轻微的正性肌力作用,其内在活性明显低于茶碱和恩丙茶碱。在离体兔乳头肌中,给予巴米茶碱至10(-3)mol/l均无作用,在较高浓度时可降低收缩力,而茶碱则剂量依赖性地增加正性肌力作用。同样在麻醉兔中,静脉注射巴米茶碱产生负性变时和变传导作用,在最高剂量时与心肌收缩力降低有关。相同等摩尔剂量的茶碱和恩丙茶碱则产生正性变时和正性肌力作用。结果表明,与其他黄嘌呤衍生物相比,巴米茶碱没有心脏刺激作用。此外,它们提示巴米茶碱对心肌的作用机制可能与Ca+(+)跨心肌膜的移动有关,该机制能够超过其抗磷酸二酯酶活性所产生的效应。