Caputo L, Tedgui A, Lévy B I
Institut National de la Santé et de la Recherche Médicale INSERM, Unit 141, IFR Circulation Lariboisière, Paris, France.
Circ Res. 1995 Aug;77(2):303-9. doi: 10.1161/01.res.77.2.303.
To investigate the relation between the tissue renin-angiotensin system (RAS) and the local vasomotor tone of large arteries, we used in vitro isolated carotid arteries from 14-week-old Wistar-Kyoto rats (WKY; n = 80) and spontaneously hypertensive rats (SHR; n = 80). Diameters were measured with the use of an ultrasonic echo-tracking system (12 MHz) under flow (2 mL/min) (F+) or no-flow (Fo) conditions, with intact endothelium (Endo+) or after endothelium removal (Endo-). The role of tissue RAS was assessed by incubating isolated carotid arteries with an angiotensin-converting enzyme inhibitor (ACE I; lisinopril, 10(-6) mol/L) or with a specific antagonist of angiotensin II AT1 receptors (AT1A; losartan, 10(-6) mol/L). In addition, maximal dilation of carotid arteries was measured after poisoning with KCN (100 mg/L). In all experiments, KCN significantly increased carotid diameters (WKY, 23 +/- 0.9%; SHR, 19 +/- 0.8%; P < .001 versus control conditions). In intact carotid arteries, flow caused significant dilation in WKY (7 +/- 0.5%, P < .001) but had no effect in SHR. In the presence or absence of flow, ACE I and AT1A induced similar dilations in both strains, and a specific antagonist of bradykinin B2 receptors (Hoe 140, 10(-7) mol/L) had no effect on ACE I-induced dilation. After endothelium removal, carotid artery diameters were significantly increased (P < .001) in both strains, although more in SHR (13 +/- 0.8%) than in WKY (8 +/- 1.1%) (P < .001). Also, flow did not modify the diameter of deendothelialized vessels and ACE I had no effect in either strain.(ABSTRACT TRUNCATED AT 250 WORDS)
为研究组织肾素 - 血管紧张素系统(RAS)与大动脉局部血管舒缩张力之间的关系,我们使用了来自14周龄Wistar - Kyoto大鼠(WKY;n = 80)和自发性高血压大鼠(SHR;n = 80)的体外分离颈动脉。在有血流(2 mL/分钟)(F +)或无血流(F0)条件下,以及在内皮完整(Endo +)或去除内皮后(Endo -),使用超声回声跟踪系统(12 MHz)测量血管直径。通过用血管紧张素转换酶抑制剂(ACE I;赖诺普利,10^(-6) mol/L)或血管紧张素II AT1受体特异性拮抗剂(AT1A;氯沙坦,10^(-6) mol/L)孵育分离的颈动脉来评估组织RAS的作用。此外,在用KCN(100 mg/L)中毒后测量颈动脉的最大扩张。在所有实验中,KCN均显著增加颈动脉直径(WKY,23±0.9%;SHR,19±0.8%;与对照条件相比,P <.001)。在内皮完整的颈动脉中,血流导致WKY显著扩张(7±0.5%,P <.001),但对SHR无影响。在有或无血流的情况下,ACE I和AT1A在两种品系中诱导相似的扩张,并且缓激肽B2受体特异性拮抗剂(Hoe 140,10^(-7) mol/L)对ACE I诱导的扩张无影响。去除内皮后,两种品系的颈动脉直径均显著增加(P <.001),尽管SHR(13±