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拉贝洛尔和普萘洛尔对自发性高血压大鼠高血压发展的影响。

The effect of labetalol and propranolol on the development of hypertension in spontaneously hypertensive rats.

作者信息

Gumułka W S, Zalewska-Rutczyńska Z

出版信息

Acta Physiol Pol. 1984 Jan-Feb;35(1):41-6.

PMID:6534080
Abstract

The effect of long-term administration of propranolol (0.2 and 0.4 mg/kg-1 p.o.) and that of labetalol (2.0, 4.0 and 8.0 mg/kg-1 p.o. and 1 mg/kg-1 i.p.) on the development of hypertension was studied in female rats of SHR/N/Ibn strain. The experiment was started on 6-week-old animals. Rats received the tested drugs once daily between 11 and 12 o'clock. From the 29th day on (i.e. after the age of 10 weeks) the arterial blood pressure was measured bloodlessly twice weekly 2 hours before the daily dose of the drug. Labetalol given p.o. in a dose of 2 mg/kg-1 had no effect on the development of hypertension, while the doses 4.0 and 8.0 mg/kg-1 decreased the arterial pressure by about 4 kPa (30 mm Hg). After drug withdrawal a rapid rise was observed in the arterial pressure to values approaching the values recorded in control animals. In the animals receiving labetalol parenterally (1 mg/kg-1 i.p.) the blood pressure was significantly lower than in control rats. After drug withdrawal the blood pressure increased gradually, however, even on the 54th day of the experiment it was slightly below that in controls. Propranolol given orally in doses of 0.2 mg/kg-1 delayed the development of hypertension, while in the dose of 0.4 mg/kg-1 it prevented its development. After withdrawal of the lower drug dose the blood pressure remained for about 2 weeks at a level similar to the previous one, later on it increased steeply to the values observed in controls.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在SHR/N/Ibn品系的雌性大鼠中,研究了长期口服普萘洛尔(0.2和0.4毫克/千克)以及拉贝洛尔(口服2.0、4.0和8.0毫克/千克以及腹腔注射1毫克/千克)对高血压发展的影响。实验从6周龄的动物开始。大鼠于每天11点至12点接受一次受试药物。从第29天起(即10周龄后),每周两次在每日给药前2小时采用无创方法测量动脉血压。口服剂量为2毫克/千克的拉贝洛尔对高血压发展无影响,而4.0和8.0毫克/千克的剂量可使动脉血压降低约4千帕(30毫米汞柱)。停药后,观察到动脉血压迅速上升至接近对照动物记录的值。腹腔注射1毫克/千克拉贝洛尔的动物血压显著低于对照大鼠。停药后血压逐渐升高,然而,即使在实验的第54天,仍略低于对照组。口服0.2毫克/千克剂量的普萘洛尔可延缓高血压的发展,而0.4毫克/千克剂量可预防其发展。较低剂量药物停药后,血压在约2周内维持在与之前相似的水平,随后急剧上升至对照值。(摘要截断于250字)

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