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体外循环期间血浆中的普萘洛尔结合情况。

Propranolol binding in plasma during cardiopulmonary bypass.

作者信息

Wood M, Shand D G, Wood A J

出版信息

Anesthesiology. 1979 Dec;51(6):512-6. doi: 10.1097/00000542-197912000-00006.

Abstract

The effect of cardiopulmonary bypass on the plasma binding of propranolol was examined in seven patients. The fraction of propranolol free in plasma doubled, increasing from 6.6 to 13.5 per cent (P less than 0.001) following the administration of heparin, 400 IU/kg. Once cardiopulmonary bypass was concluded and protamine, 8 mg/kg, given, the free fraction decreased from 13.4 to 8.7 per cent (P less than 0.005). There was a further significant decrease to 6.5 per cent over the next 3.1 hours (SE +/- 0.3). Those alterations in the free fraction, which would result in more drug being available for binding to receptor sites and for exerting its pharmacologic effect, were due principally to the changes in free fatty acid levels produced by heparin and protamine, but also to the hemodilution produced by the pump prime.

摘要

研究了体外循环对7例患者血浆中普萘洛尔结合率的影响。给予400 IU/kg肝素后,血浆中游离普萘洛尔的比例增加了一倍,从6.6%增至13.5%(P<0.001)。体外循环结束并给予8 mg/kg鱼精蛋白后,游离比例从13.4%降至8.7%(P<0.005)。在接下来的3.1小时内,游离比例进一步显著降至6.5%(标准误±0.3)。游离比例的这些变化会使更多药物能够与受体部位结合并发挥药理作用,其主要原因是肝素和鱼精蛋白引起的游离脂肪酸水平变化,同时也与泵预充液导致的血液稀释有关。

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