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氯丙嗪对狗体内普萘洛尔的处置及β-肾上腺素能阻断活性的影响。

Effects of chlorpromazine on the disposition and beta-adrenergic blocking activity of propranolol in the dog.

作者信息

Bai S A, Abramson F P

出版信息

J Pharmacokinet Biopharm. 1984 Jun;12(3):333-49. doi: 10.1007/BF01061724.

Abstract

The effects of chlorpromazine (100 mg p.o., 2 hr before propranolol) on the disposition and beta-adrenergic blocking actions of both intravenous (6 mg) and oral (40 mg) propranolol were studied in the dog. Chlorpromazine pretreatment significantly reduced (69%) the oral clearance of propranolol, resulting in significant increases in propranolol bioavailability (159%), and in the total beta-adrenergic blocking activity (111%) after the oral dose. The increase in the total beta-adrenergic blocking activity of oral propranolol after chlorpromazine pretreatment was mostly due to an increased contribution from the parent compound; the apparent activity from active propranolol metabolites was not affected by chlorpromazine. Chlorpromazine pretreatment had no significant influence on the systemic clearance, elimination half-life, apparent volume of distribution, and plasma binding of propranolol, or on the apparent hepatic blood flow. After intravenous propranolol, chlorpromazine pretreatment had no effect on either the total amount of beta-adrenergic blocking activity or the amount of activity attributable to active metabolites. The decreased oral propranolol clearance by chlorpromazine was seen as a shift to the left in the propranolol dose vs. AUC relationship, eliminating the apparent nonlinear kinetic behavior of oral propranolol, and reducing the apparent oral threshold dose. Chlorpromazine's major, if not only, effect on propranolol disposition was to reduce the presystemic elimination of propranolol, possibly through inhibition of its metabolism via a pathway other than ring oxidation.

摘要

研究了氯丙嗪(口服100毫克,在普萘洛尔给药前2小时)对犬静脉注射(6毫克)和口服(40毫克)普萘洛尔的处置及β-肾上腺素能阻断作用的影响。氯丙嗪预处理显著降低了普萘洛尔的口服清除率(69%),导致普萘洛尔生物利用度显著增加(159%),且口服给药后总β-肾上腺素能阻断活性增加(111%)。氯丙嗪预处理后口服普萘洛尔总β-肾上腺素能阻断活性的增加主要归因于母体化合物的贡献增加;活性普萘洛尔代谢物的表观活性不受氯丙嗪影响。氯丙嗪预处理对普萘洛尔的全身清除率、消除半衰期、表观分布容积、血浆结合率或表观肝血流量均无显著影响。静脉注射普萘洛尔后,氯丙嗪预处理对β-肾上腺素能阻断活性总量或活性代谢物所致活性量均无影响。氯丙嗪使口服普萘洛尔清除率降低,表现为普萘洛尔剂量与AUC关系向左移位,消除了口服普萘洛尔明显的非线性动力学行为,并降低了表观口服阈剂量。氯丙嗪对普萘洛尔处置的主要(如果不是唯一)作用是减少普萘洛尔的首过消除,可能是通过抑制其除环氧化以外的代谢途径。

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