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呋塞米的利尿和降压作用。

Diuretic and antihypertensive actions of furosemide.

作者信息

Hutcheon D E, Leonard G

出版信息

J Clin Pharmacol J New Drugs. 1967 Jan-Feb;7(1):26-33. doi: 10.1002/j.1552-4604.1967.tb00026.x.

Abstract

Furosemide (4 - chloro - N - (2 - furyl - methyl) - 5 - sulfamoylanthranilic acid) caused a prompt increase in sodium, potassium, and chloride excretions in patients with chronic congestive heart failure. Doses of 50, 100, and 200 mg orally produced progressively increasing diuretic responses. When given over a period of one week to patients with essential hypertension, furosemide in doses of 100 to 200 mg orally per day caused a significant decrease in systolic and diastolic pressure. A significant lowering of blood pressure was also demonstrated in hypertensive patients treated with furosemide over a period of one year. Biochemical alterations during furosemide administration included elevation of fasting blood sugar levels in patients with diabetes mellitus, increased uric acid concentrations, and lowering of plasma potassium levels. All biochemical changes were reversible when the drug was discontinued. No evidence of hematologic or hepatic dysfunction was observed in 16 patients who received furosemide in a daily dose of 40 to 160 mg over a 52-week period. Although furosemide has been recommended primarily for the treatment of edema refractory to other forms of therapy, long-term studies indicate that the drug is also capable of maintaining patients with chronic congestive heart failure without producing serious systemic toxicity.

摘要

速尿(4-氯-N-(2-呋喃甲基)-5-氨磺酰基邻氨基苯甲酸)可使慢性充血性心力衰竭患者的钠、钾和氯排泄迅速增加。口服50、100和200毫克剂量可产生逐渐增强的利尿反应。当给原发性高血压患者服用一周时,每天口服100至200毫克速尿可使收缩压和舒张压显著降低。在接受速尿治疗一年的高血压患者中也显示出血压显著降低。速尿给药期间的生化改变包括糖尿病患者空腹血糖水平升高、尿酸浓度增加和血钾水平降低。停药后所有生化变化均可逆转。在16名患者中,他们在52周内每天服用40至160毫克速尿,未观察到血液学或肝功能障碍的证据。虽然速尿主要推荐用于治疗对其他治疗形式无效的水肿,但长期研究表明,该药物也能够维持慢性充血性心力衰竭患者,而不会产生严重的全身毒性。

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