Halushka P V, Wohltmann H, Privitera P J, Hurwitz G, Margolius H S
Ann Intern Med. 1977 Sep;87(3):281-6. doi: 10.7326/0003-4819-87-3-281.
The urinary excretions of prostaglandin E-like material (iPGE) and kallikrein were measured in two children with Bartter's syndrome. Urinary iPGE excretion was three and 10 times greater than normal, and urinary kallikrein was five and 10 times greater than normal in the two subjects. Furthermore, excretions of iPGE and kallikrein were highly correlated (P less than 0.005) with each other before and during treatment with indomethacin, a prostaglandin synthetase inhibitor. Indomethacin significantly (P less than 0.001) reduced urinary iPGE, urinary kallikrein, and plasma renin activity, while increasing the sensitivity to intravenous angiotensin II and the serum potassium to normal. The results confirm that renal prostaglandins may be involved in the pathogenesis of Bartter's syndrome and suggest that renal prostaglandins and the kallikrein-kinin system are linked.
对两名患有巴特综合征的儿童进行了前列腺素E样物质(iPGE)和激肽释放酶的尿排泄量测定。两名受试者的尿iPGE排泄量分别比正常水平高3倍和10倍,尿激肽释放酶则分别比正常水平高5倍和10倍。此外,在使用前列腺素合成酶抑制剂吲哚美辛治疗之前和治疗期间,iPGE和激肽释放酶的排泄量彼此高度相关(P<0.005)。吲哚美辛显著(P<0.001)降低了尿iPGE、尿激肽释放酶和血浆肾素活性,同时增加了对静脉注射血管紧张素II的敏感性,并使血清钾恢复正常。结果证实,肾前列腺素可能参与巴特综合征的发病机制,并提示肾前列腺素与激肽释放酶-激肽系统相关联。