van Dijk D J, Boner G, Giler S, Erman A
Institute of Hypertension and Kidney Diseases, Rabin Medical Center, Tel-Aviv, Israel.
J Renin Angiotensin Aldosterone Syst. 2001 Sep;2(3):193-8. doi: 10.3317/jraas.2001.027.
The renin-angiotensin system (RAS) plays an important role in the regulation of blood pressure, electrolyte balance and renal function in normal human pregnancy. The present study was designed to assess various components of the RAS and renal function during pregnancy and immediately after pregnancy in the streptozotocin (STZ)-diabetic rat.
Pregnant Wistar rats were allocated to three groups: I-control, non-diabetic rats (n=24), II-STZ-diabetic rats (STZ 55 mg/kg body weight, i.v. on day 10 of pregnancy, n=24), III-diabetic rats, as above, treated with insulin (4 units/day, s.c. n=21). On days 17-18 of pregnancy, or within 24 hours after delivery, the rats were sacrificed and the various components of the RAS were determined.
Urinary protein excretion (UP) and creatinine clearance(CCr) were greater in group II, four days after STZ, than in group I (UP: I-7.6+/-2.8, II-18.6+/-6.3 mg/24-hour, p<0.001, CCr: I-1.04+/-0.33, II-2.38+/-0.7 ml/minute, p<0.001). Mean (+/-SD) serum angiotensin-converting enzyme (ACE) activity and plasma angiotensin II(Ang II) levels at days 17-18 of pregnancy were greater in the untreated diabetic rats than in control pregnant rats (ACE: 163+/-18 vs. 111+/-21 nmol/ml/minute, p<0.001, Ang II: 115+/-45 vs. 43+/-10 pg/ml, p<0.005). Postpartum serum ACE activity and plasma Ang II levels were greater in group II (ACE: I-123+/-14, II-142+/-24, III-108+/-21 nmol/ml/minute, p<0.01, Ang II: I-56+/-38, II-148+/-62, III-38+/-17 pg/mI, p<0.001). ACE activity in the lung was greater, whereas the activity in the renal cortex was less, in group II than in group I. Kidney weight in untreated diabetic rats was greater than in the other two groups.
Increased serum ACE activity during pregnancy and postpartum in the untreated diabetic rat is associated with enhanced serum Ang II levels, which may contribute to increased protein excretion and renal hypertrophy.
肾素 - 血管紧张素系统(RAS)在正常人类妊娠期间血压、电解质平衡及肾功能的调节中发挥重要作用。本研究旨在评估链脲佐菌素(STZ)诱导的糖尿病大鼠在孕期及产后即刻RAS的各个组分及肾功能情况。
将怀孕的Wistar大鼠分为三组:I组 - 对照组,非糖尿病大鼠(n = 24);II组 - STZ糖尿病大鼠(孕期第10天静脉注射55 mg/kg体重的STZ,n = 24);III组 - 糖尿病大鼠,如上述,接受胰岛素治疗(4单位/天,皮下注射,n = 21)。在妊娠第17 - 18天或分娩后24小时内,处死大鼠并测定RAS的各个组分。
STZ注射后4天,II组的尿蛋白排泄量(UP)和肌酐清除率(CCr)高于I组(UP:I组 - 7.6±2.8,II组 - 18.6±6.3 mg/24小时,p<0.001;CCr:I组 - 1.04±0.33,II组 - 2.38±0.7 ml/分钟,p<0.001)。妊娠第17 - 18天,未治疗的糖尿病大鼠的平均(±标准差)血清血管紧张素转换酶(ACE)活性和血浆血管紧张素II(Ang II)水平高于对照孕鼠(ACE:163±18对111±21 nmol/ml/分钟,p<0.001;Ang II:115±45对43±10 pg/ml,p<0.005)。产后II组的血清ACE活性和血浆Ang II水平更高(ACE:I组 - 123±14,II组 - 142±24,III组 - 108±21 nmol/ml/分钟,p<0.01;Ang II:I组 - 56±38,II组 - 148±62,III组 -