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在哮喘患者中口服特布他林。

Oral administration of terbutaline in asthmatic patients.

作者信息

Ripe E, Hörnblad Y, Tegnér K

出版信息

Eur J Respir Dis Suppl. 1984;134:171-9.

PMID:6586478
Abstract

The absorption and excretion profiles of orally administered terbutaline were investigated in 10 asthmatic patients who received a solution containing 5 mg of [3H]terbutaline sulphate. Bronchodilating effect and side-effects were followed. The mean serum concentration curve reached its maximum of 3.0 +/- 0.3 (SEM) ng/mL at 60-90 min. Renal clearance data indicated that terbutaline was excreted only via glomerular filtration. Approximately 30% of the dose was excreted in the urine in 12 h and 40% in 72 h. Three compounds appeared in the urine: unchanged terbutaline, a sulphate conjugate, and a glucuronide, the main metabolite being the sulphate conjugate. The maximum mean increase in volume of air expelled in the first second of forced expiration (FEV1) was 35%, attained 90-120 min after intake of terbutaline. There was a correlation (r = 0.74) between the serum level and the bronchodilator effect. No significant effects on heart rate or blood pressure were found. Tremor, as objectively measured with the aid of an accelerometer, was experienced by the patients when it increased to twice its basal level. The observed tremor did not appear to parallel either the serum level or the bronchodilating effect. A comparative study in 3 of the patients showed that [3H]terbutaline formulated as a tablet had similar bioavailability.

摘要

在10名哮喘患者中研究了口服特布他林的吸收和排泄情况,这些患者服用了含有5毫克[³H]硫酸特布他林的溶液。同时观察了支气管扩张作用和副作用。血清浓度曲线在60 - 90分钟时达到最大值,为3.0±0.3(标准误)纳克/毫升。肾脏清除率数据表明,特布他林仅通过肾小球滤过排泄。约30%的剂量在12小时内随尿液排出,40%在72小时内排出。尿液中出现了三种化合物:未变化的特布他林、一种硫酸酯结合物和一种葡萄糖醛酸结合物,主要代谢产物是硫酸酯结合物。用力呼气第一秒呼出气体量(FEV1)的最大平均增加量为35%,在摄入特布他林后90 - 120分钟达到。血清水平与支气管扩张作用之间存在相关性(r = 0.74)。未发现对心率或血压有显著影响。借助加速度计客观测量发现,当震颤增加到基础水平的两倍时,患者会出现震颤。观察到的震颤似乎与血清水平或支气管扩张作用均无平行关系。对3名患者进行的一项对比研究表明,制成片剂的[³H]特布他林具有相似的生物利用度。

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