Suppr超能文献

硝苯地平与多潘立酮在高血压患者中的血流动力学(全身和肾脏)及体液相互作用。

Haemodynamic (systemic and renal) and humoral interactions between nicardipine and domperidone in hypertensives.

作者信息

Lucarini A R, Salvetti A

机构信息

Clinica Medica I, University of Pisa, Italy.

出版信息

J Hypertens Suppl. 1987 Dec;5(5):S571-4.

PMID:3327930
Abstract

We studied the haemodynamic (systemic and renal) and humoral effects of nicardipine, a dihydropyridine calcium entry blocker in essential hypertensives and whether DA2 dopaminergic receptor blockade, induced by domperidone, might modify these effects. Eight uncomplicated mild to moderate hypertensives received placebo (saline) for 30 min followed by i.v. nicardipine (0.06 mg/min) for 30 min and repeated the same sequence introducing domperidone (10 mg i.v.) between saline and nicardipine; the effects of each treatment were followed for 30 min. The sequence was randomized with a 72-h interval between each study. Compared with placebo, nicardipine significantly reduced mean blood pressure (-14%) and renovascular resistance (-28%), increased heart rate (+15%), renal plasma flow (RPF; +21%), glomerular filtration rate (GFR; +43%) and urinary sodium excretion (+181%). The acute natriuretic effect of nicardipine was associated with an increase in the amount of filtered sodium (+43%) and with fractional sodium excretion (+110%), and a direct correlation was found between changes in RPF and in urinary sodium excretion (r = 0.68) and fractional sodium excretion (r = 0.57). Plasma renin activity (PRA) did not change, plasma aldosterone was significantly reduced (-10%) and plasma noradrenaline significantly increased (+63%). Domperidone pretreatment prevented the GFR increase induced by nicardipine and increased the noradrenaline response (+107%), but did not change the other actions of nicardipine. These data show that nicardipine, when acutely infused in essential hypertensives, while reducing blood pressure and reflexly activating the sympathetic nervous system, significantly increases urinary sodium excretion, RPF and GFR.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们研究了二氢吡啶类钙通道阻滞剂尼卡地平对原发性高血压患者的血流动力学(全身和肾脏)及体液影响,以及由多潘立酮诱导的DA2多巴胺能受体阻滞是否会改变这些影响。8例无并发症的轻度至中度高血压患者先接受30分钟的安慰剂(生理盐水)静脉输注,随后接受30分钟的尼卡地平静脉输注(0.06毫克/分钟),并重复相同顺序,在生理盐水和尼卡地平之间加入多潘立酮(静脉注射10毫克);每种治疗的效果持续观察30分钟。该顺序是随机的,每次研究之间间隔72小时。与安慰剂相比,尼卡地平显著降低平均血压(-14%)和肾血管阻力(-28%),增加心率(+15%)、肾血浆流量(RPF;+21%)、肾小球滤过率(GFR;+43%)和尿钠排泄(+181%)。尼卡地平的急性利钠作用与滤过钠量增加(+43%)和钠排泄分数增加(+110%)相关,并且发现RPF变化与尿钠排泄变化(r = 0.68)和钠排泄分数变化(r = 0.57)之间存在直接相关性。血浆肾素活性(PRA)未改变,血浆醛固酮显著降低(-10%),血浆去甲肾上腺素显著增加(+63%)。多潘立酮预处理可防止尼卡地平诱导的GFR增加,并增强去甲肾上腺素反应(+107%),但不改变尼卡地平的其他作用。这些数据表明,在原发性高血压患者中急性输注尼卡地平时,在降低血压并反射性激活交感神经系统的同时,可显著增加尿钠排泄、RPF和GFR。(摘要截选至250字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验