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中枢注射苄amil对 Dahl S 大鼠高血压的影响。

Effect of central infusion of benzamil on Dahl S rat hypertension.

作者信息

Gomez-Sanchez E P, Gomez-Sanchez C E

机构信息

Research Service, Harry S Truman Memorial Veterans Hospital, Columbia, Missouri, USA.

出版信息

Am J Physiol. 1995 Sep;269(3 Pt 2):H1044-7. doi: 10.1152/ajpheart.1995.269.3.H1044.

DOI:10.1152/ajpheart.1995.269.3.H1044
PMID:7573500
Abstract

The effect of continuous central infusion of benzamil, a Na+ channel-selective amiloride analogue, on the salt-induced hypertension in inbred Dahl salt-sensitive (SS/jr) rats was assessed. The continuous intracerebroventricular or subcutaneous infusion of benzamil at doses which have no effect when infused systemically was started at the same time or 2 wk after saline was substituted for drinking water, when the rats' blood pressures had become significantly elevated. Within 13 days, drinking saline caused a similar and significant increase in the blood pressures of rats receiving the vehicle intracerebroventricularly and 1 microgram/h of benzamil subcutaneously, which persisted throughout the 4-wk experiment. The intracerebroventricular infusion of 1 or 0.3 microgram/h benzamil, started at the same time the salt challenge was instituted, significantly deterred the increase in blood pressure over 4 wk. The intracerebroventricular, but not the subcutaneous, infusion of benzamil at 0.5 microgram/h arrested the increase in blood pressure in rats that were already hypertensive after 12 days on saline. Within 3 days the pressures in the intracerebroventricular and subcutaneous benzamil groups became significantly different, due to the further increase of the blood pressure in those animals receiving the intracerebroventricular vehicle with subcutaneous benzamil. There was no significant difference in weight gain throughout the experiment or in 24-h urine volumes and urinary Na(+)-to-K+ ratio at days 5 and 12 of benzamil infusion between groups.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

评估了持续脑室内输注苯扎米(一种钠通道选择性氨氯地平类似物)对近交系 Dahl 盐敏感(SS/jr)大鼠盐诱导高血压的影响。当大鼠血压显著升高时,在改用盐水作为饮用水的同时或 2 周后,开始持续脑室内或皮下输注苯扎米,其剂量在全身输注时无作用。在 13 天内,饮用盐水使脑室内接受载体和皮下接受 1 微克/小时苯扎米的大鼠血压出现相似且显著的升高,并在整个 4 周实验中持续存在。在开始盐负荷的同时开始脑室内输注 1 或 0.3 微克/小时苯扎米,可显著抑制 4 周内血压的升高。脑室内而非皮下输注 0.5 微克/小时苯扎米可阻止在饮用盐水 12 天后已患高血压大鼠的血压升高。3 天内,脑室内和皮下苯扎米组的血压出现显著差异,这是由于接受脑室内载体和皮下苯扎米的动物血压进一步升高所致。各组在整个实验期间的体重增加、苯扎米输注第 5 天和第 12 天的 24 小时尿量及尿钠钾比均无显著差异。(摘要截断于 250 字)

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