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茶碱对麻醉犬心肌反应性充血的时间依赖性影响。

Time-dependent effects of theophylline on myocardial reactive hyperaemias in the anaesthetized dog.

作者信息

Gidday J M, Esther J W, Ely S W, Rubio R, Berne R M

机构信息

Department of Physiology, University of Virginia Health Sciences Center, Charlottesville 22908.

出版信息

Br J Pharmacol. 1990 May;100(1):95-101. doi: 10.1111/j.1476-5381.1990.tb12058.x.

Abstract
  1. The effects of a loading dose of theophylline (5 mg kg-1 i.v.) on the hyperaemias resulting from short-term (15 and 30 s) interruptions in coronary blood flow and intracoronary adenosine were studied at given intervals over a 2 h period in the anaesthetized dog. 2. These hyperaemic responses were affected differently by theophylline and each effect was time-dependent. The reactive hyperaemic response progressively decreased after drug delivery, reaching 46% of control at 2 h. In contrast, after a maximal attenuation to 23% of control 5 min after theophylline, the hyperaemia resulting from intracoronary adenosine progressively increased over the same period, reaching 64% of control 2 h after the loading dose. 3. Two-compartment model results based on plasma theophylline measurements and the time course of theophylline accumulation in pericardial infusates, suggested that complete drug distribution throughout the heart may require at least 20 min following a single intravenous dose. 4. If it is assumed that theophylline blocks coronary vascular adenosine receptors, these pharmacokinetics are consistent with the time-dependent pattern of response attenuation we observed for the adenosine-induced hyperaemias, but they cannot entirely explain the pattern of response attenuation observed for the occlusion-induced hyperaemias. The continued increase in attenuation of this response after complete drug distribution suggests an additional pharmacodynamic action of theophylline. 5. We conclude that a single therapeutic dose of theophylline results in distinct time-dependent pharmacological effects with respect to the ability of the coronary vasculature to dilate in response to temporary interruptions in oxygen supply and in response to exogenously administered adenosine. These effects deserve consideration in both experimental studies in which adenosine antagonists are used to assess adenosine action in vivo, and in clinical practice where theophylline pharmacotherapy for pulmonary disorders is commonplace.
摘要
  1. 在麻醉犬身上,研究了静脉注射负荷剂量氨茶碱(5毫克/千克)对冠状动脉血流短期中断(15秒和30秒)及冠状动脉内注射腺苷所导致的充血的影响,在2小时内按给定间隔进行观察。2. 氨茶碱对这些充血反应的影响各不相同,且每种影响都与时间相关。给药后反应性充血反应逐渐降低,2小时时降至对照值的46%。相反,氨茶碱给药5分钟后最大程度衰减至对照值的23%,冠状动脉内注射腺苷所导致的充血在同一时期逐渐增加,负荷剂量后2小时达到对照值的64%。3. 基于血浆氨茶碱测量值及心包灌注液中氨茶碱蓄积的时间过程的二室模型结果表明,单次静脉给药后,药物在心脏内完全分布可能至少需要20分钟。4. 如果假设氨茶碱阻断冠状动脉血管腺苷受体,这些药代动力学与我们观察到的腺苷诱导充血反应衰减的时间依赖性模式一致,但不能完全解释闭塞诱导充血反应衰减的模式。药物完全分布后该反应衰减的持续增加提示氨茶碱存在额外的药效学作用。5. 我们得出结论,单次治疗剂量的氨茶碱就冠状动脉血管对暂时中断供氧及外源性给予腺苷的扩张能力而言,会产生明显的时间依赖性药理作用。在使用腺苷拮抗剂评估体内腺苷作用的实验研究以及茶碱用于肺部疾病药物治疗很常见的临床实践中,都应考虑这些作用。

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本文引用的文献

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Role of adenosine in postocclusion coronary vasodilation.
Am J Physiol. 1980 Feb;238(2):H214-9. doi: 10.1152/ajpheart.1980.238.2.H214.
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4
Theophylline. A "state of the art" review.茶碱。一篇“前沿技术”综述。
Pharmacotherapy. 1983 Jan-Feb;3(1):2-44. doi: 10.1002/j.1875-9114.1983.tb04531.x.
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Adenosine receptors and behavioral actions of methylxanthines.腺苷受体与甲基黄嘌呤的行为作用
Proc Natl Acad Sci U S A. 1981 May;78(5):3260-4. doi: 10.1073/pnas.78.5.3260.
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Kinetics of pharmacologic effects.药理效应动力学
Clin Pharmacol Ther. 1966 May-Jun;7(3):362-72. doi: 10.1002/cpt196673362.

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