Schwertschlag U, Hackenthal E
Naunyn Schmiedebergs Arch Pharmacol. 1982 Jun;319(3):239-42. doi: 10.1007/BF00495872.
The renal effects of histamine, histamine receptor agonists and antagonists were studied in the isolated rat kidney, which was perfused with a synthetic medium at constant perfusion pressure in a single pass system. Histamine induced a concentration-dependent increase of renin release ranging from a two-fold increase at 0.5 microM to a four-fold increase at 10 microM. No change in renal vascular resistance, glomerular filtration rate and sodium excretion occurred. Histamine-H2-antagonists (ranitidine and cimetidine) were more effective to block the response to histamine than was the histamine H1-antagonist diphenhydramine. Histamine-H2-agonists (impromidine and dimaprit, 2.5 microM each) were potent stimulators of renin release, their effect was blunted by H2-antagonists. The histamine-H1-agonist pyridyl-2-ethylamine had a low stimulatory activity at 10 microM final concentration, which may reflect partial H2-agonistic effects. It is concluded that histamine stimulates renin release via H2-receptor activation.
在离体大鼠肾脏中研究了组胺、组胺受体激动剂和拮抗剂对肾脏的作用,该离体肾脏在单通道系统中以恒定灌注压力用合成培养基进行灌注。组胺诱导肾素释放呈浓度依赖性增加,从0.5微摩尔时增加两倍到10微摩尔时增加四倍。肾血管阻力、肾小球滤过率和钠排泄没有变化。组胺H2拮抗剂(雷尼替丁和西咪替丁)比组胺H1拮抗剂苯海拉明更有效地阻断对组胺的反应。组胺H2激动剂(每一种均为2.5微摩尔的英普咪定和二甲替啶)是肾素释放的有效刺激剂,它们的作用被H2拮抗剂减弱。组胺H1激动剂吡啶-2-乙胺在终浓度为10微摩尔时具有低刺激活性,这可能反映了部分H2激动效应。得出的结论是,组胺通过H2受体激活刺激肾素释放。