Kröll F, Karlsson J A, Ryrfeldt A, Persson C G
Department of Clinical Pharmacology, University Hospital, Lund, Sweden.
Pulm Pharmacol. 1988;1(2):85-92. doi: 10.1016/s0952-0600(88)80004-8.
Effects of purine nucleosides and asthma mediators on airway tone have been examined in the guinea-pig isolated perfused lung preparation. Acetylcholine (10 pmol-0.3 nmol), histamine (1-10 nmol), adenosine (10 nmol-0.3 mumol), ATP (10 nmol-0.3 mumol) and inosine (10 mumol-0.1 mmol) all produced a dose dependent increase in lung resistance (RL) and a decrease in dynamic compliance (CDYN). ATP was equipotent with adenosine whereas inosine was about 500 times less potent. The adenosine-induced bronchoconstriction was affected neither by disodium cromoglycate (150 microM) nor by the histamine H1-receptor antagonist, mepyramine (1 microM) suggesting that histamine is not involved in this response. Furthermore, it was studied whether the xanthines theophylline and enprofylline specifically interacted with the adenosine induced bronchoconstriction. Theophylline significantly (P less than 0.01-0.001) and concentration dependently prevented both acetylcholine and adenosine-induced increase in RL. The response to 0.1 nmol acetylcholine was reduced by 32.8 +/- 8.4% (mean +/- SEM) and 58.1 +/- 4.0%, respectively, by 75 and 150 microM theophylline. Theophylline, 75 and 150 microM, also inhibited the increase in RL caused by 0.1 mumol of adenosine by 61.4 +/- 9.6% and 83.4 +/- 5.2%, respectively. Theophylline, was significantly (P less than 0.05-0.01) more potent in preventing the RL increase produced by adenosine than that by acetylcholine. Enprofylline, 30 microM, equally well as 75 microM theophylline reduced the acetylcholine-induced bronchoconstriction by 41.8 +/- 7.6% (P less than 0.001).(ABSTRACT TRUNCATED AT 250 WORDS)
在豚鼠离体灌注肺标本中研究了嘌呤核苷和哮喘介质对气道张力的影响。乙酰胆碱(10皮摩尔 - 0.3纳摩尔)、组胺(1 - 10纳摩尔)、腺苷(10纳摩尔 - 0.3微摩尔)、ATP(10纳摩尔 - 0.3微摩尔)和肌苷(10微摩尔 - 0.1毫摩尔)均使肺阻力(RL)呈剂量依赖性增加,动态顺应性(CDYN)降低。ATP与腺苷的效力相当,而肌苷的效力约低500倍。色甘酸钠(150微摩尔)和组胺H1受体拮抗剂美吡拉敏(1微摩尔)均不影响腺苷诱导的支气管收缩,提示组胺不参与此反应。此外,还研究了黄嘌呤类药物茶碱和恩丙茶碱是否与腺苷诱导的支气管收缩特异性相互作用。茶碱显著(P小于0.01 - 0.001)且呈浓度依赖性地抑制乙酰胆碱和腺苷诱导的RL增加。75和150微摩尔的茶碱分别使对0.1纳摩尔乙酰胆碱的反应降低32.8±8.4%(平均值±标准误)和58.1±4. %。75和150微摩尔的茶碱也分别使由0.1微摩尔腺苷引起的RL增加抑制61.4±9.6%和83.4±5.2%。茶碱在预防腺苷引起的RL增加方面比乙酰胆碱更有效(P小于0.05 - 0.01)。30微摩尔的恩丙茶碱与75微摩尔的茶碱一样,使乙酰胆碱诱导的支气管收缩降低41.8±7.6%(P小于0.001)。(摘要截短于250字)