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母亲和新生儿血浆药物结合及α1-酸性糖蛋白的变化。

Changes in plasma drug binding and alpha 1-acid glycoprotein in mother and newborn infant.

作者信息

Wood M, Wood A J

出版信息

Clin Pharmacol Ther. 1981 Apr;29(4):522-6. doi: 10.1038/clpt.1981.73.

Abstract

A number of drugs bind to alpha 1-acid glycoprotein in plasma. To determine whether age-related changes in alpha 1-acid glycoprotein influence drug binding in mother and newborn infant and also the effects of sex, pregnancy, and oral contraceptives on drug binding, the binding of lidocaine, diazepam, propranolol, d-tubocurarine, and metocurine was determined by equilibrium dialysis in 17 men, 16 nonpregnant women, 16 nonpregnant women on oral contraceptives, and 15 mothers and their newborn infants at delivery. The free fraction of d-tubocurarine (p less than 0.05), metocurine (p less than 0.01), propranolol (p less than 0.001), and lidocaine (p less than 0.02) was higher in neonatal blood than in maternal blood, whereas the free fraction of diazepam was less in fetal cord blood than the mother's (p less than 0.02), but higher than that in nonpregnant women (p less than 0.001). The free fractions of diazepam, propranolol, and lidocaine were higher (p less than 0.001) in pregnant women compared with nonpregnant women while the diazepam and lidocaine free fractions were higher (p less than 0.05) in nonpregnant women and oral contraceptives than in women not using them. Alpha 1-acid glycoprotein was lower in the fetus (15.3 +/- 4.7 mg/100 ml) than the mother (49.6 +/- 6.5 mg/100 ml) (p less than 0.002). There was a positive correlation between plasma alpha 1-acid glycoprotein concentrations and the binding ratio (bound/free concentrations) of lidocaine (p less than 0.001; r = 0.623) and propranolol (p less than 0.001); r = 0.652), indicating that it is likely that the elevation of the free fraction of these drugs in the fetus is due in part to lower levels of alpha 1-acid glycoprotein.

摘要

许多药物与血浆中的α1-酸性糖蛋白结合。为了确定α1-酸性糖蛋白的年龄相关变化是否会影响母婴体内的药物结合,以及性别、妊娠和口服避孕药对药物结合的影响,通过平衡透析法测定了17名男性、16名未怀孕女性、16名口服避孕药的未怀孕女性以及15名产妇及其新生儿分娩时利多卡因、地西泮、普萘洛尔、d-筒箭毒碱和米库氯铵的结合情况。d-筒箭毒碱(p<0.05)、米库氯铵(p<0.01)、普萘洛尔(p<0.001)和利多卡因(p<0.02)在新生儿血液中的游离分数高于母体血液,而地西泮在胎儿脐带血中的游离分数低于母体(p<0.02),但高于未怀孕女性(p<0.001)。与未怀孕女性相比,孕妇体内地西泮、普萘洛尔和利多卡因的游离分数更高(p<0.001),而未怀孕女性口服避孕药后地西泮和利多卡因的游离分数高于未服用者(p<0.05)。胎儿体内的α1-酸性糖蛋白(15.3±4.7mg/100ml)低于母体(49.6±6.5mg/100ml)(p<0.002)。血浆α1-酸性糖蛋白浓度与利多卡因(p<0.001;r=0.623)和普萘洛尔(p<0.001;r=0.652)的结合率(结合/游离浓度)呈正相关,表明胎儿体内这些药物游离分数的升高可能部分归因于α1-酸性糖蛋白水平较低。

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