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普萘洛尔的药代动力学药物相互作用。

Pharmacokinetic drug interactions with propranolol.

作者信息

Wood A J, Feely J

出版信息

Clin Pharmacokinet. 1983 May-Jun;8(3):253-62. doi: 10.2165/00003088-198308030-00004.

DOI:10.2165/00003088-198308030-00004
PMID:6342901
Abstract

Propranolol is widely used in clinical practice and is frequently administered along with other drugs. The co-administration of propranolol and other drugs may result in either propranolol-induced changes in the disposition of other drugs or in effects of the other drugs on the pharmacokinetics of propranolol. These changes may be due to alteration in absorption, metabolism or to haemodynamic effects such as altered liver blood flow. Understanding the pharmacokinetics of propranolol is important to the rational interpretation of the effects of other drugs on propranolol's disposition. The absorption, protein binding and metabolism of propranolol may all be affected by the co-administration of other drugs. Induction of propranolol's metabolism by halofenate, phenytoin, phenobarbitone, rifampicin and alcohol have all been implicated in altering propranolol clearance, while inhibition of hepatic drug metabolising enzymes by chlorpromazine and cimetidine appear to reduce propranolol clearance. Propranolol may also affect the metabolism of other drugs such as antipyrine, chlorpromazine, theophylline and thyroid hormones. Suggestions that propranolol may alter quinidine's elimination have not been substantiated. By reducing liver blood flow propranolol may reduce the systemic clearance of other high extraction drugs such as lignocaine.

摘要

普萘洛尔在临床实践中广泛应用,且常与其他药物联合使用。普萘洛尔与其他药物联合使用可能导致普萘洛尔引起其他药物处置的变化,或者其他药物对普萘洛尔药代动力学产生影响。这些变化可能是由于吸收、代谢改变,或者是由于血流动力学效应,如肝血流量改变。了解普萘洛尔的药代动力学对于合理诠释其他药物对普萘洛尔处置的影响很重要。普萘洛尔的吸收、蛋白结合和代谢都可能受到其他药物联合使用的影响。卤芬酯、苯妥英、苯巴比妥、利福平和酒精对普萘洛尔代谢的诱导作用均与普萘洛尔清除率改变有关,而氯丙嗪和西咪替丁对肝药酶的抑制作用似乎会降低普萘洛尔的清除率。普萘洛尔也可能影响其他药物的代谢,如安替比林、氯丙嗪、茶碱和甲状腺激素。关于普萘洛尔可能改变奎尼丁消除的说法尚未得到证实。通过减少肝血流量,普萘洛尔可能会降低其他高摄取药物如利多卡因的全身清除率。

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本文引用的文献

1
Reduction of liver blood flow and propranolol metabolism by cimetidine.西咪替丁对肝血流量及普萘洛尔代谢的影响
N Engl J Med. 1981 Mar 19;304(12):692-5. doi: 10.1056/NEJM198103193041202.
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Effects of acute alcohol administration on propranolol absorption.急性酒精摄入对普萘洛尔吸收的影响。
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Effects of metoprolol and propranolol on theophylline elimination.美托洛尔和普萘洛尔对茶碱消除的影响。
艾司洛尔降低麻醉需求,从而有助于早期拔管:一项针对接受颅内手术患者的前瞻性对照研究。
BMC Anesthesiol. 2015 Nov 28;15:172. doi: 10.1186/s12871-015-0154-1.
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Comparison of effects of intraoperative esmolol and ketamine infusion on acute postoperative pain after remifentanil-based anesthesia in patients undergoing laparoscopic cholecystectomy.比较依托咪酯和氯胺酮输注对瑞芬太尼麻醉后行腹腔镜胆囊切除术患者急性术后疼痛的影响。
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A study of the interaction between ropranolol and NSAIDs in protein binding by gel filtration method.通过凝胶过滤法研究普萘洛尔与非甾体抗炎药在蛋白质结合方面的相互作用。
Indian J Clin Biochem. 2006 Mar;21(1):121-5. doi: 10.1007/BF02913079.
6
The antinociceptive effect of esmolol.艾司洛尔的镇痛作用。
Korean J Anesthesiol. 2010 Sep;59(3):141-3. doi: 10.4097/kjae.2010.59.3.141. Epub 2010 Sep 20.
7
beta-blockers. Drug interactions of clinical significance.β受体阻滞剂。具有临床意义的药物相互作用。
Drug Saf. 1995 Dec;13(6):359-70. doi: 10.2165/00002018-199513060-00005.
8
Lack of a pharmacokinetic interaction between carvedilol and digitoxin or phenprocoumon.
Eur J Clin Pharmacol. 1993;44(6):583-6. doi: 10.1007/BF02440864.
9
Extent of beta 1- and beta 2-receptor occupancy in plasma assesses the antagonist activity of metoprolol, pindolol, and propranolol in the elderly.血浆中β1和β2受体占有率可评估美托洛尔、吲哚洛尔和普萘洛尔在老年人中的拮抗活性。
Cardiovasc Drugs Ther. 1993 Dec;7(6):839-49. doi: 10.1007/BF00877714.
10
Pharmacokinetic and pharmacodynamic interaction study of diazepam and metoprolol.地西泮与美托洛尔的药代动力学和药效学相互作用研究。
Eur J Clin Pharmacol. 1984;26(2):223-6. doi: 10.1007/BF00630289.
Clin Pharmacol Ther. 1980 Oct;28(4):463-7. doi: 10.1038/clpt.1980.189.
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Reduction in lidocaine clearance during continuous infusion and by coadministration of propranolol.连续输注利多卡因以及与普萘洛尔合用时,利多卡因清除率降低。
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4-Hydroxypropranolol and its glucuronide after single and long-term doses of propranolol.单次及长期服用普萘洛尔后的4-羟基普萘洛尔及其葡糖醛酸苷。
Clin Pharmacol Ther. 1980 Jan;27(1):22-31. doi: 10.1038/clpt.1980.4.
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Am J Psychiatry. 1982 Sep;139(9):1198-9. doi: 10.1176/ajp.139.9.1198.