Tamm C, Favre L, Spence S, Pfister S, Vallotton M B
Department of Medicine, University Hospital, Geneva, Switzerland.
Eur J Clin Pharmacol. 1989;37(1):17-21. doi: 10.1007/BF00609417.
Oxindanac, a moderately active cyclo-oxygenase inhibitor in vitro, is a new antiinflammatory agent under clinical investigation. Its effects on frusemide-induced natriuresis have now been studied. Eight male volunteers receiving frusemide 40 mg b.d. were also given either oxindanac 300 mg b.d. or placebo in two consecutive periods separated by a treatment-free period, according to a randomized cross-over study design. Urinary prostaglandin excretion (PGF2 alpha) fell by 75% after 3 days on oxindanac. Frusemide-induced renin activity reached 66% of the control value in the presence of oxindanac. However, the natriuresis induced by frusemide did not differ significantly whether oxindanac or placebo was administered, despite the inhibitory action of the former on prostaglandin synthesis in vivo.
羟吲哚酸,一种在体外具有中等活性的环氧化酶抑制剂,是一种正在进行临床研究的新型抗炎药。现已对其对速尿诱导的利钠作用的影响进行了研究。根据随机交叉研究设计,8名每天服用40毫克速尿的男性志愿者在两个连续的时间段内,分别接受每天300毫克羟吲哚酸或安慰剂治疗,两个时间段之间有一个无治疗期。服用羟吲哚酸3天后,尿前列腺素排泄量(PGF2α)下降了75%。在服用羟吲哚酸的情况下,速尿诱导的肾素活性达到对照值的66%。然而,尽管羟吲哚酸在体内对前列腺素合成有抑制作用,但无论给予羟吲哚酸还是安慰剂,速尿诱导的利钠作用均无显著差异。