Kasai Y, Abe K, Yasujima M, Tajima J, Seino M, Chiba S, Sato K, Goto T, Omata K, Tanno M
Tohoku J Exp Med. 1983 Dec;141(4):417-22. doi: 10.1620/tjem.141.417.
Acute effects of MK421 were examined in 11 male normal volunteers. Oral administration of 5 mg of MK421 did not induce any changes in blood pressure or pulse rate. Plasma renin activity increased significantly from 7.3 +/- 2.9 ng/ml to 22.2 +/- 7.1 (p less than 0.05), whereas plasma aldosterone concentration did not change. Blood kinin, or urinary excretion of kallikrein and of prostaglandin E did not change. However, urinary excretion of sodium increased significantly from 44.0 +/- 6.8 mEq/4 hr to 56.5 +/- 6.5 (p less than 0.02) following the administration of MK421. The present results show that an increased renin release induced by MK421 is independent of change in blood pressure, and also suggest that MK421 may have a direct action on the renal tubules.
在11名男性正常志愿者身上研究了MK421的急性效应。口服5毫克MK421未引起血压或脉搏率的任何变化。血浆肾素活性从7.3±2.9纳克/毫升显著增加至22.2±7.1(p<0.05),而血浆醛固酮浓度未改变。血激肽、激肽释放酶的尿排泄量以及前列腺素E的尿排泄量均未改变。然而,服用MK421后,钠的尿排泄量从44.0±6.8毫当量/4小时显著增加至56.5±6.5(p<0.02)。目前的结果表明,MK421诱导的肾素释放增加与血压变化无关,并且还提示MK421可能对肾小管有直接作用。