首页> 美国卫生研究院文献>Postgraduate Medical Journal >Absence of potentiation of the skin response to intradermal bradykinin by a long-acting angiotensin converting enzyme inhibitor trandolapril at conventional antihypertensive dosage in human volunteers: a double-blind randomized cross-over placebo-controlled trial.
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Absence of potentiation of the skin response to intradermal bradykinin by a long-acting angiotensin converting enzyme inhibitor trandolapril at conventional antihypertensive dosage in human volunteers: a double-blind randomized cross-over placebo-controlled trial.

机译:在人类志愿者中使用常规降压剂量的长效血管紧张素转换酶抑制剂trandolapril不能增强皮肤对皮内缓激肽的反应:双盲随机交叉安慰剂对照试验。

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摘要

A double-blind, randomized, cross-over, placebo-controlled study was carried out to determine the extent and duration of potentiation of the action of bradykinin introduced intradermally by a long-acting novel angiotensin converting enzyme (ACE) inhibitor, trandolapril. The investigations were performed in a temperature and humidity-controlled laboratory. Intradermal injections of 1 microgram, 2.5 micrograms and 5 micrograms of bradykinin and normal saline (as control) were made into the forearm skin of eight healthy normotensive male volunteers aged 21-33 years (mean 28 years) at baseline, 2, 4, 8, 24, 48, 72 and 96 hours after either 2 mg trandolapril or placebo given orally. Skin blood flow outside the induced weal was monitored by laser Doppler flowmetry (mean of recordings at four sites adjacent to the weal within the flare area). Flare area and weal volume were also measured. Trandolapril reduced the mean arterial pressure. However, there was no evidence that this activity was associated with a potentiation of the cutaneous action of bradykinin. In conclusion, it would appear that potentiation of the action of bradykinin may not be an important contributing factor to the fall in total peripheral vascular resistance associated with ACE inhibition in humans in the control of hypertension.
机译:进行了一项双盲,随机,交叉,安慰剂对照研究,以确定长效新型血管紧张素转化酶(ACE)抑制剂trandolapril在皮内引入缓激肽作用的作用增强的程度和持续时间。研究是在温度和湿度受控的实验室中进行的。在基线,2、4、8时,对年龄在21-33岁(平均28岁)的8位健康的血压正常男性志愿者的前臂皮肤进行了1微克,2.5微克和5微克缓激肽和生理盐水(作为对照)的皮内注射。口服2 mg trandolapril或安慰剂后第24、48、72和96小时。通过激光多普勒血流仪(在耀斑区域内与血脂相邻的四个位置处的记录平均值)监控诱导血脂外的皮肤血流量。还测量了喇叭口面积和体积。 Trandolapril降低了平均动脉压。但是,没有证据表明这种活性与缓激肽的皮肤作用增强有关。总之,在控制高血压的人中,缓激肽的作用增强可能不是导致与ACE抑制相关的总外周血管阻力下降的重要因素。

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