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腺苷和三磷酸腺苷对患者房室传导的影响。

Effect of adenosine and adenosine-5'-triphosphate on atrioventricular conduction in patients.

作者信息

Favale S, Di Biase M, Rizzo U, Belardinelli L, Rizzon P

出版信息

J Am Coll Cardiol. 1985 May;5(5):1212-9. doi: 10.1016/s0735-1097(85)80027-9.

Abstract

This study was carried out to further elucidate the effects of adenosine and adenosine-5'-triphosphate (ATP) on atrioventricular (AV) conduction in patients. Adenosine (0.24 mg/kg) and ATP (0.28 mg/kg) were administered intravenously to 37 patients undergoing intracardiac electrophysiologic evaluation. Both adenosine and ATP depressed AV conduction by lengthening the atrial to His bundle (AH) interval. The effects of adenosine and ATP after rapid intravenous bolus administration were fast in onset (15 +/- 0.5 and 15 +/- 1.5 s, respectively), but transient in duration (10.5 +/- 0.5 s for ATP and 17 +/- 3 s for adenosine). Although muscarinic blockade with 0.04 mg/kg atropine shortened the AH interval from a control value of 123 +/- 12 to 74 +/- 4 ms, it did not modify the effects of adenosine or ATP, or both (that is, latency and duration of the effects were not significantly different from before atropine administration). In contrast, aminophylline, a competitive antagonist of adenosine, completely prevented the effects of adenosine and ATP. Aminophylline alone also shortened the AH interval from a control value of 98 +/- 9 to 74 +/- 9 ms. This decrease was blocked by propranolol (0.1 mg/kg), whereas propranolol did not influence the ability of aminophylline to antagonize the effects of adenosine or ATP, or both. Thus, the catecholamines released by aminophylline are unlikely to account for the ability of aminophylline to antagonize the effects of adenosine and ATP. In conclusion, these findings indicate that intravenously administered adenosine and ATP are equally effective in producing AV block that is antagonized by aminophylline but not by atropine.

摘要

本研究旨在进一步阐明腺苷和三磷酸腺苷(ATP)对患者房室传导的影响。对37例接受心内电生理评估的患者静脉注射腺苷(0.24mg/kg)和ATP(0.28mg/kg)。腺苷和ATP均通过延长心房至希氏束(AH)间期来抑制房室传导。快速静脉推注后,腺苷和ATP的作用起效迅速(分别为15±0.5秒和15±1.5秒),但持续时间短暂(ATP为10.5±0.5秒,腺苷为17±3秒)。尽管用0.04mg/kg阿托品进行毒蕈碱阻断可使AH间期从123±12毫秒的对照值缩短至74±4毫秒,但它并未改变腺苷或ATP或两者的作用(即作用的潜伏期和持续时间与阿托品给药前相比无显著差异)。相比之下,腺苷的竞争性拮抗剂氨茶碱完全阻断了腺苷和ATP的作用。单独使用氨茶碱也可使AH间期从98±9毫秒的对照值缩短至74±9毫秒。这种缩短被普萘洛尔(0.1mg/kg)阻断,而普萘洛尔并不影响氨茶碱拮抗腺苷或ATP或两者作用的能力。因此,氨茶碱释放的儿茶酚胺不太可能解释氨茶碱拮抗腺苷和ATP作用的能力。总之,这些发现表明静脉注射腺苷和ATP在产生房室传导阻滞方面同样有效,且这种阻滞可被氨茶碱拮抗,但不能被阿托品拮抗。

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