首页> 外文期刊>Hypertension: An Official Journal of the American Heart Association >Effects of alpha 1-blockade on arterial compliance in normotensive and hypertensive rats.
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Effects of alpha 1-blockade on arterial compliance in normotensive and hypertensive rats.

机译:α1受体阻滞对正常血压和高血压大鼠动脉顺应性的影响。

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The effects of blockade of alpha 1-adrenergic receptors on the mechanical properties of the arterial wall were studied in 10 spontaneously hypertensive rats (SHR) as compared with 10 matched normotensive Wistar-Kyoto (WKY) rats. Ascending aortic pressure and flow were recorded in open-chest anesthetized rats, and the systemic arterial compliance was calculated. Intravenous injection (1 mg/kg) of Urapidil, a selective alpha 1-adrenergic antagonist, induced a significant decrease in arterial pressure (-26%, p less than 0.01 and -37%, p less than 0.001 in WKY rats and SHR, respectively) without significant changes in cardiac output. In control conditions, systemic arterial compliance was lower in SHR (3.29 +/- 1.52 microliters/mm Hg) than in WKY rats (4.35 +/- 1.35 microliters/mm Hg, p less than 0.01). Urapidil injection induced significant increases in systemic arterial compliance values in both strains (p less than 0.001). In another set of experiments (15 WKY rats and 15 SHR), the carotid compliance (microliters/mm Hg) was determined from the arterial volume-pressure relation under control conditions, after local incubation with Urapidil, and after total abolition of the vascular smooth muscle by KCN. In WKY rats, the carotid compliance increased markedly after incubation with Urapidil at doses corresponding to 1 mg/kg (+31%, p less than 0.01). A further increase in the carotid compliance was observed after KCN poisoning (+11%, p less than 0.05). In SHR, incubation with Urapidil at doses corresponding to 2 mg/kg were necessary to induce a significant increase in compliance (+38%). At this dosage, there was no further increase in compliance after KCN poisoning.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:与10只正常血压的Wistar-Kyoto(WKY)大鼠相比,在10只自发性高血压大鼠(SHR)中研究了α1-肾上腺素受体阻断对动脉壁力学性能的影响。记录开胸麻醉大鼠的升主动脉压力和流量,并计算全身动脉顺应性。静脉注射(1 mg / kg)的Urapidil,一种选择性的α1-肾上腺素能拮抗剂,导致WKY大鼠和SHR的动脉压显着降低(-26%,p小于0.01和-37%,p小于0.001,并没有明显的心输出量变化。在对照条件下,SHR(3.29 +/- 1.52微升/毫米汞柱)的全身动脉顺应性低于WKY大鼠(4.35 +/- 1.35微升/毫米汞柱,p小于0.01)。乌拉地尔注射液在两种菌株中均导致全身动脉顺应性值显着增加(p小于0.001)。在另一组实验中(15只WKY大鼠和15只SHR),在对照条件下,与Urapidil进行局部温育以及完全消除血管平滑肌后,根据动脉体积-压力关系确定颈动脉顺应性(微升/ mm Hg)。 KCN制作的肌肉。在WKY大鼠中,以1 mg / kg的剂量与Urapidil孵育后,颈动脉顺应性显着增加(+ 31%,p小于0.01)。 KCN中毒后观察到颈动脉顺应性进一步增加(+ 11%,p小于0.05)。在SHR中,与Urapidil以2 mg / kg的剂量温育是诱导依从性显着增加(+ 38%)所必需的。在此剂量下,KCN中毒后依从性没有进一步增加。(摘要以250字截断)

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