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Effects of cholestyramine and colestipol on the plasma concentrations of propranolol.

机译:消胆胺和考来替泊对心得安的血浆浓度的影响。

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摘要

The effect of equivalent hypolipidaemic doses of cholestyramine (8 g) or colestipol (10 g) on the plasma concentrations of propranolol and 4'-hydroxypropranolol was studied in 12 normal volunteers following the oral administration of 120 mg of normal release propranolol tablets. When two doses of either cholestyramine or colestipol were administered prior to the propranolol, the peak plasma concentrations and area under the curve for both propranolol and the metabolite 4'-hydroxypropranolol were reduced significantly (P less than 0.05). We conclude that the drug interaction between cholestyramine or colestipol and propranolol leads to significant reductions in plasma concentrations of propranolol and 4'-hydroxypropranolol which may cause a clinically diminished effect for a given dosage. Therefore, patients should be observed when either of these resins are added to or deleted from a therapeutic regimen.
机译:在口服120 mg正常释放的普萘洛尔片剂后,在12名正常志愿者中研究了当量降血脂剂量的胆固醇(8 g)或colestipol(10 g)对普萘洛尔和4'-羟基普萘洛尔血浆浓度的影响。在普萘洛尔之前服用两剂胆甾醇胺或考来替泊时,普萘洛尔和代谢物4'-羟基普萘洛尔的血浆峰值浓度和曲线下面积均显着降低(P小于0.05)。我们得出的结论是,胆甾胺或colestipol与普萘洛尔之间的药物相互作用导致血浆中普萘洛尔和4'-羟基普萘洛尔的浓度显着降低,这对于给定剂量可能会导致临床效果减弱。因此,当在治疗方案中添加或删除这些树脂中的任何一种时,应观察患者。

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