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地高辛与庆大霉素之间的一些药代动力学和药效学相互作用。

Some pharmacokinetic and pharmacodynamic interactions between digoxin and gentamicin.

作者信息

Staneva-Stoytcheva D, Kristeva E, Prodanova K

机构信息

Institute of Physiology, Bulgarian Academy of Sciences, Sofia.

出版信息

Acta Physiol Pharmacol Bulg. 1991;17(4):27-36.

PMID:1668708
Abstract

Some pharmacokinetic and pharmacodynamic interactions between digoxin and gentamicin were studied in experiments on rabbits, guinea-pigs and cats. An increase of digoxin serum levels and changes in some basic pharmacokinetic parameters of digoxin (t1/2 alpha, t1/2 beta, AUC, AL) were established in gentamicin-pretreated rabbits, the changes being dependent on the dose and schedule of administration. Most pronounced were the changes in digoxin kinetics during simultaneous 5-day treatment with digoxin (0.035 mg/kg i. p.) and nontoxic doses (10 and 2 mg/kg) of gentamicin. The toxicity of digoxin in guinea-pigs, assessed by lethal doses of digoxin, was increased only after the highest dose of gentamicin (100 mg/kg), while after nontoxic or close to therapeutic doses (10 and 2 mg/kg) of gentamicin the digoxin toxicity was not changed or was even decreased. Digoxin decreased the nerve-muscle blocking effect of gentamicin on cat ischiadicus-gastrocnemius preparation. The possible mechanisms involved are discussed.

摘要

在兔子、豚鼠和猫身上进行的实验研究了地高辛和庆大霉素之间的一些药代动力学和药效学相互作用。在庆大霉素预处理的兔子中,地高辛血清水平升高,且地高辛的一些基本药代动力学参数(t1/2α、t1/2β、AUC、AL)发生变化,这些变化取决于给药剂量和给药方案。在同时用地高辛(0.035mg/kg腹腔注射)和无毒剂量(10和2mg/kg)的庆大霉素进行为期5天的治疗期间,地高辛动力学变化最为明显。通过地高辛致死剂量评估,豚鼠体内地高辛的毒性仅在最高剂量的庆大霉素(100mg/kg)后增加,而在无毒或接近治疗剂量(10和2mg/kg)的庆大霉素后,地高辛毒性未改变甚至降低。地高辛降低了庆大霉素对猫坐骨神经-腓肠肌标本的神经肌肉阻滞作用。文中讨论了可能涉及的机制。

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