肝素对急性和慢性缺氧大鼠血流动力学和结构反应的影响。

L M Hu, R Geggel, P Davies, L Reid
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引用次数: 0

摘要

在小鼠中,间歇性给予肝素,已被证明可以减少缺氧引起的右心室肥厚(RVH)。我们在大鼠身上研究了肝素对缺氧引起的血流动力学和肺血管结构重塑的影响,特别是外周动脉的新肌肉化。以30和50 u/kg/h两种剂量的肝素,通过微渗透泵连续静脉输注给大鼠,观察其对平均肺动脉压(PPa)、RVH的影响,并利用形态计量学技术观察血管结构重塑。缺氧产生了先前在该模型中描述的血流动力学和结构变化。肝素对PPa无显著影响;高剂量肝素组RVH略有降低。肝素治疗后,缺氧引起的轴向肺动脉管腔狭窄减少:肝素降低了动脉肌肉化的比例,特别是在肺泡管水平,其中周细胞是前体平滑肌细胞。肝素并没有减少肌肉动脉内侧厚度的增加和外径的减小。有些大鼠在慢性缺氧后,对急性缺氧没有反应,但在其他血流动力学和结构特征上与“应答者”没有什么不同。包括所有大鼠在内,肝素对缺氧的平均急性升压反应不受影响:仅在有反应的大鼠中,肝素明显降低了急性缺氧时PPa的升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of heparin on the haemodynamic and structural response in the rat to acute and chronic hypoxia.

In the mouse, heparin administered intermittently, has been shown to reduce the right ventricular hypertrophy (RVH) caused by hypoxia. We have investigated in the rat the effect of heparin on the haemodynamic and pulmonary vascular structural remodelling produced by hypoxia, with special reference to the new muscularization of peripheral arteries. Heparin at one of two doses (30 and 50 u/kg/h) was administered by continuous intravenous infusion from a miniosmotic pump to rats during 10 days exposure to hypobaric hypoxia and its effect examined on mean pulmonary artery pressure (PPa), RVH and, using morphometric techniques, vascular structural remodelling. Hypoxia produced the haemodynamic and structural changes previously described in this model. Heparin had no significant effect on PPa; a slight reduction in RVH was seen in the high-dose heparin group. After heparin, the narrowing of the axial pulmonary artery lumen caused by hypoxia was less: heparin reduced the proportion of arteries that became muscularized, particularly at alveolar duct level where the pericyte is the precursor smooth muscle cell. Heparin did not diminish the increase in medial thickness or reduction in external diameter of muscular arteries. Some rats, after chronic hypoxia, did not respond to an acute hypoxic challenge yet were no different from 'responders' in other haemodynamic and structural features. Including all rats, the mean acute pressor response to hypoxia was unaffected by heparin: taking only responder rats, a trend was apparent that heparin reduced the rise in PPa on acute hypoxic challenge.

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