Kuznetsova L V, Medvedeva N A, Medvedev O S
Biull Eksp Biol Med. 1993 Jun;115(6):594-6.
The hemodynamic effect of combined V2/V1 arginine vasopressin (AVP) antagonist in conscious rats with acute 24 hour streptozotocin (STZ)--induced diabetes was studied using the microsphere technique. The rats were made diabetic with a single intravenous injection of STZ (60 mg/kg). One day after STZ administration the hemodynamic parameters in the experimental animals were measured before and 10 minutes after AVP antagonist injection (50 mg/kg, i.v.). The hemodynamic alterations observed post-antagonist included: 1) an increase in the total peripheral resistance (1.84 +/- 0.15 vs. 1.31 +/- 0.12 mm Hg/ml/min per 100 g before antagonist administration, p < 0.05), 2) a decrease in the cardiac index (49.0 +/- 3.1 vs. 68.7 +/- 5.2 ml/min/100 g before antagonist administration, p < 0.05) and stroke volume (0.40 +/- 0.03 vs. 0.57 +/- 0.06 ml before antagonist administration, p < 0.05), 3) a significant (p < 0.05) decrease in the blood flow to the skin, skeletal muscle, stomach, small intestine and kidneys. The mean arterial pressure and heart rate remained unchangeable post-antagonist. These data suggest that AVP is responsible, at least in part, for prominent hemodynamic alterations observed in conscious rats with 24 hour STZ-induced diabetes.
采用微球技术研究了V2/V1精氨酸加压素(AVP)联合拮抗剂对急性链脲佐菌素(STZ)诱导糖尿病清醒大鼠的血流动力学影响。通过单次静脉注射STZ(60mg/kg)使大鼠患糖尿病。在给予STZ一天后,测量实验动物在注射AVP拮抗剂(50mg/kg,静脉注射)前和注射后10分钟的血流动力学参数。拮抗剂注射后观察到的血流动力学改变包括:1)总外周阻力增加(拮抗剂给药前为1.31±0.12mmHg/ml/min per 100g,给药后为1.84±0.15,p<0.05),2)心脏指数降低(拮抗剂给药前为68.7±5.2ml/min/100g,给药后为49.0±3.1,p<0.05)和每搏输出量降低(拮抗剂给药前为0.57±0.06ml,给药后为0.40±0.03,p<0.05),3)皮肤、骨骼肌、胃、小肠和肾脏的血流量显著降低(p<0.05)。拮抗剂注射后平均动脉压和心率保持不变。这些数据表明,AVP至少在一定程度上导致了24小时STZ诱导糖尿病清醒大鼠中观察到的显著血流动力学改变。