Li X C, Widdop R E
Department of Pharmacology, Monash University, Clayton, Victoria, Australia.
Hypertension. 1995 Dec;26(6 Pt 1):989-97. doi: 10.1161/01.hyp.26.6.989.
Angiotensin II subtype 1 (AT1) receptor antagonists reduce mean arterial pressure in various experimental models of hypertension, including two-kidney, one clip (2K1C) renal hypertension. However, the regional hemodynamic mechanisms underlying the hypotensive effect of AT1 receptor antagonists in 2K1C rats under dynamic conditions have not been documented. Therefore, in the present study we determined the hemodynamic profile of the AT1 receptor antagonist CV-11974 in conscious 2K1C rats and sham-operated control rats. Approximately 4 weeks after clipping, rats underwent a further two-stage operation for implantation of Doppler flow probes on the contralateral (left) renal artery, superior mesenteric artery, and distal aorta as well as for the implantation of intravascular catheters. At least 24 hours after the last operation continuous recordings were made of mean arterial pressure; heart rate; and renal, mesenteric, and hindquarters flows and conductances (Doppler shift/mean arterial pressure) in response to three doses of CV-11974 (0.01, 0.1, and 1.0 mg/kg i.v.). CV-11974 caused a small hypotensive effect (decrease of approximately 15 mm Hg) in the sham group, but regional flows and vascular conductances did not change. By contrast, in 2K1C rats CV-11974 caused dose-dependent hypotension that was maximal (-19 +/- 6, -41 +/- 4, and -51 +/- 8 mm Hg, respectively) after 6 hours. These changes were associated with generalized vasodilatation (increased conductance) in all three vascular beds, although there were subtle differences with the different CV-11974 doses.(ABSTRACT TRUNCATED AT 250 WORDS)
血管紧张素II 1型(AT1)受体拮抗剂可降低多种高血压实验模型中的平均动脉压,包括两肾一夹(2K1C)肾性高血压模型。然而,动态条件下AT1受体拮抗剂在2K1C大鼠中产生降压作用的局部血流动力学机制尚未见报道。因此,在本研究中,我们测定了AT1受体拮抗剂CV - 11974对清醒2K1C大鼠和假手术对照大鼠的血流动力学影响。夹闭后约4周,大鼠接受进一步的两阶段手术,在对侧(左)肾动脉、肠系膜上动脉和主动脉远端植入多普勒血流探头,并植入血管内导管。最后一次手术后至少24小时,连续记录平均动脉压、心率以及肾、肠系膜和后肢的血流和传导率(多普勒频移/平均动脉压),以响应三种剂量的CV - 11974(0.01、0.1和1.0 mg/kg静脉注射)。CV - 11974在假手术组引起轻微降压作用(约降低15 mmHg),但局部血流和血管传导率未发生变化。相比之下,在2K1C大鼠中,CV - 11974引起剂量依赖性低血压,6小时后达到最大值(分别为-19±6、-41±4和-51±8 mmHg)。这些变化与所有三个血管床的广泛性血管舒张(传导率增加)相关,尽管不同剂量的CV - 11974存在细微差异。(摘要截短至250字)