Fujita S, Ishida Y, Izumi K, Moritoki H, Ohara M, Takei M
Br J Pharmacol. 1980 Feb;68(2):343-9. doi: 10.1111/j.1476-5381.1980.tb10423.x.
1 Dilazep, a coronary dilator, has been reported to potentiate the negative inotropic and negative chronotropic responses of guinea-pig atria to adenosine. Studies were made on the mechanism of the potentiating action of dilazep with special reference to the degradation and uptake of adenosine. 2 The negative inotropic actions of adenosine and adenine nucleotides, such as ATP, ADP, AMP and cyclic AMP, on guinea-pig atria were selectively and dose-dependently augmented by dilazep at concentrations insufficient to produce any effect alone (0.01 to 1 microM). 3 Incubation of atrial tissue with 8.8 nM adenosine, containing 0.1 microCi of [3H]-adenosine, resulted in accumulation of [3H]-adenosine in the tissue; dilazep (0.01 to 1 microM) inhibited this accumulation. 4 Adenosine (10 microM to 10 mM) was degraded to inosine and hypoxanthine during incubation with atrial tissue; dilazep (0.1 to 10 microM) retarded the disappearance of adenosine and the formation of inosine and hypoxanthine. 5 These results suggest that dilazep potentiates the negative inotropic effect of adenosine on guinea-pig atria by preventing both its accumulation by atrial tissue and degradation by deaminase.
1 已报道冠脉扩张剂地拉卓可增强豚鼠心房对腺苷的负性肌力和负性变时反应。特别参照腺苷的降解和摄取,对地拉卓增强作用的机制进行了研究。2 地拉卓在不足以单独产生任何作用的浓度(0.01至1微摩尔)下,可选择性且剂量依赖性地增强腺苷及腺嘌呤核苷酸(如ATP、ADP、AMP和环磷腺苷)对豚鼠心房的负性肌力作用。3 用含0.1微居里[³H] - 腺苷的8.8纳摩尔腺苷孵育心房组织,导致组织中[³H] - 腺苷蓄积;地拉卓(0.01至1微摩尔)抑制这种蓄积。4 腺苷(10微摩尔至10毫摩尔)在与心房组织孵育期间降解为次黄苷和次黄嘌呤;地拉卓(0.1至10微摩尔)延缓腺苷的消失以及次黄苷和次黄嘌呤的形成。5 这些结果表明,地拉卓通过阻止心房组织对腺苷的蓄积以及脱氨酶对其的降解,增强了腺苷对豚鼠心房的负性肌力作用。