Stepniakowski K, Lapiński M, Noszczyk B, Januszewicz A, Szczepańska-Sadowska E
Department of Clinical and Applied Physiology, Medical Academy, Warszawa, Poland.
Pol J Pharmacol Pharm. 1991 Nov-Dec;43(6):487-93.
The aim of the present study was to compare effects of intravenous infusion of vasopressin AVP and V1 receptors blockade on blood pressure and heart rate in normotensive (WKY) and spontaneously hypertensive (SHR) rats. A 20 min vasopressin infusion (1.2 ng/kg/min) elicited significantly greater increase in mean blood pressure (MP) in SHR than in WKY. Heart rate was significantly reduced in SHR while nonsignificantly in WKY. A 20 min dEt2 AVP (V1 antagonist) infusion (0.5 microgram/kg/min) elicited significant decrease in MP and increase in heart rate (HR) in SHR, but produced no effect in WKY. The data indicate that SHR are more susceptible to pressor and hypotensive effects of sustained elevation of AVP and AVP antagonist. The results support the hypothesis that AVP may contribute to pathogenesis of hypertension.
本研究的目的是比较静脉输注血管加压素(AVP)和V1受体阻断对正常血压(WKY)大鼠和自发性高血压(SHR)大鼠血压和心率的影响。持续20分钟输注血管加压素(1.2 ng/kg/分钟)后,SHR的平均血压(MP)升高幅度显著大于WKY。SHR的心率显著降低,而WKY的心率无显著变化。持续20分钟输注dEt2 AVP(V1拮抗剂,0.5微克/千克/分钟)可使SHR的MP显著降低,心率(HR)升高,但对WKY无影响。数据表明,SHR对AVP持续升高和AVP拮抗剂的升压及降压作用更敏感。这些结果支持了AVP可能参与高血压发病机制的假说。