Hiruta M, Furuhashi N, Tanaka M, Takahashi T, Kohno H, Suzuki M
Nihon Sanka Fujinka Gakkai Zasshi. 1986 Feb;38(2):177-80.
In this study, urinary kallikrein quantity and activity were measured by the kallikrein direct RIA and kininogenase activity with human low molecular weight kininogen in 32 non pregnant healthy women, 20 normal 3rd trimester pregnant women and 18 3rd trimester hypertension type toxemia patients. There was no significant difference in urinary kallikrein quantity between non pregnant women (n = 32, 64.0 +/- 6.3 micrograms/day, mean +/- SE) and normal pregnant women (n = 20, 68.1 +/- 10.1 micrograms/day). There was a significant difference (p less than 0.001) between non pregnant women and toxemia patients (n = 18, 22.5 +/- 3.3 micrograms/day). There was a significant difference (p less than 0.001) between toxemia patients and normal pregnant women. There was a significant difference (p less than 0.05) in urinary kallikrein activity between non pregnant women (n = 32, 496.2 +/- 57.2 micrograms kinin/day) and normal pregnant women (n = 20, 319.5 +/- 48.1 micrograms kinin/day). There was a significant difference (p less than 0.0001) between non pregnant women and toxemia patients (n = 18, 82.6 +/- 13.6 micrograms kinin/day). There was a significant difference (p less than 0.01) between normal pregnant women and toxemia patients. There were no correlation in both urinary kallikrein quantity and activity between severe type toxemia patients (systolic blood pressure greater than or equal to 160mmHg or diastolic blood pressure greater than or equal to 110mmHg) and mild type toxemia patients (160mmHg greater than systolic blood pressure greater than or equal to 140mmHg and 110mmHg greater than diastolic blood pressure greater than or equal to 90mmHg).(ABSTRACT TRUNCATED AT 250 WORDS)
在本研究中,采用激肽释放酶直接放射免疫分析法测定了32名未孕健康女性、20名孕晚期正常孕妇和18名孕晚期高血压型毒血症患者的尿激肽释放酶含量及活性,并用人低分子量激肽原测定了激肽原酶活性。未孕女性(n = 32,64.0±6.3微克/天,均值±标准误)与正常孕妇(n = 20,68.1±10.1微克/天)的尿激肽释放酶含量无显著差异。未孕女性与毒血症患者(n = 18,22.5±3.3微克/天)之间存在显著差异(p<0.001)。毒血症患者与正常孕妇之间存在显著差异(p<0.001)。未孕女性(n = 32,496.2±57.2微克激肽/天)与正常孕妇(n = 20,319.5±48.1微克激肽/天)的尿激肽释放酶活性存在显著差异(p<0.05)。未孕女性与毒血症患者(n = 18,82.6±13.6微克激肽/天)之间存在显著差异(p<0.0001)。正常孕妇与毒血症患者之间存在显著差异(p<0.01)。重度毒血症患者(收缩压≥160mmHg或舒张压≥110mmHg)与轻度毒血症患者(160mmHg>收缩压≥140mmHg且110mmHg>舒张压≥90mmHg)的尿激肽释放酶含量及活性均无相关性。(摘要截选至250词)