Van der Meer P, de Jong J W
Thoraxcenter, Erasmus University Rotterdam, The Netherlands.
Am J Physiol. 1990 Sep;259(3 Pt 2):H759-65. doi: 10.1152/ajpheart.1990.259.3.H759.
To test whether inosine interferes with the action of adenosine, we investigated the effects of intracoronary administration of inosine, adenosine, 8-phenyltheophylline, and adenosine deaminase on isolated rat heart. Inosine did not change heart rate or developed tension but increased the effluent adenosine concentration. Inosine also decreased exogenous adenosine uptake and breakdown. After the start of the inosine infusion (20 microM), a transient 30% decrease of coronary flow took place within 0.5 min. The nucleoside caused sustained vasodilation, dependent on the concentration (30-400 microM). After the infusion we observed a transient vasodilation. A nonvasoactive inosine concentration (10 microM) combined with an adenosine concentration that increased flow by 60% (0.1 microM) raised vasodilation by another 60%. Infusion of adenosine, adenosine deaminase, or 8-phenyltheopylline did not influence the inosine-induced transient decrease of flow, suggesting that this decrease is independent of adenosine and its receptor. We conclude that inosine 1) potentiates the vasodilation induced by adenosine and 2) is a coronary vasodilator but probably also a vasoconstrictor.
为了测试肌苷是否会干扰腺苷的作用,我们研究了冠状动脉内注射肌苷、腺苷、8-苯基茶碱和腺苷脱氨酶对离体大鼠心脏的影响。肌苷并未改变心率或舒张张力,但增加了流出液中腺苷的浓度。肌苷还减少了外源性腺苷的摄取和分解。在开始输注肌苷(20微摩尔)后,冠状动脉血流量在0.5分钟内出现短暂的30%下降。这种核苷引起持续的血管舒张,其程度取决于浓度(30 - 400微摩尔)。输注后我们观察到短暂的血管舒张。非血管活性浓度的肌苷(10微摩尔)与使血流量增加60%的腺苷浓度(0.1微摩尔)相结合,使血管舒张程度再提高60%。输注腺苷、腺苷脱氨酶或8-苯基茶碱均未影响肌苷诱导的血流量短暂下降,这表明这种下降与腺苷及其受体无关。我们得出结论:1)肌苷增强了腺苷诱导的血管舒张;2)肌苷是一种冠状动脉血管舒张剂,但可能也是一种血管收缩剂。