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首页> 外文期刊>American Journal of Physiology >Aneurysm-type plexiform lesions form in supernumerary arteries in pulmonary arterial hypertension: potential therapeutic implications
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Aneurysm-type plexiform lesions form in supernumerary arteries in pulmonary arterial hypertension: potential therapeutic implications

机译:肺动脉高血压中占状动脉中的动脉瘤型络合物形状:潜在的治疗意义

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摘要

Histological observations in human pulmonary arterial hypertension (PAH) suggest a link between plexiform lesions and pulmonary supernumerary arteries. Pulmonary microvascular endothelial cells are characterized as hyperproliferative and progenitor-like. This study investigates the hypothesis that aneurysm-type plexiform lesions form in pulmonary supernumerary arteries because of their anatomical properties and endothelial characteristics similar to pulmonary microvascular endothelial cells. To induce PAH, rats were injected with Sugen5416, and exposed to hypoxia (10% O_2) for 3 days (early stage) or 3 wk (mid-stage), or 3 wk of hypoxia with an additional 10 wk of normoxia (late-stage PAH). We examined morphology of pulmonary vasculature and vascular remodeling in lung serial sections from PAH and normal rats. Aneurysm-type plexiform lesions formed in small side branches of pulmonary arteries with morphological characteristics similar to supernumerary arteries. Over the course of PAH development, the number of Ki67-positive cells increased in small pulmonary arteries, including supernumerary arteries, whereas the number stayed consistently low in large pulmonary arteries. The increase in Ki67-positive cells was delayed in supernumerary arteries compared with small pulmonary arteries. In late-stage PAH, -90% of small unconventional side branches that were likely to be supernumerary arteries were nearly closed. These results support our hypothesis that supernumerary arteries are the predominant site for aneurysm-type plexiform lesions in Sugen5416/hypoxia/normoxia-exposed PAH rats partly because of the combination of their unique anatomical properties and the hyperproliferative potential of endothelial cells. We propose that the delayed and extensive occlusive lesion formation in supernumerary arteries could be a preventive therapeutic target in patients with PAH.
机译:人肺动脉高血压(PAH)中的组织学观察表明丛状病变与肺叠观术中的联系。肺部微血管内皮细胞的特征在于过度增殖和祖先样。本研究调查了由于其解剖学性质和内皮特性与肺部微血管内皮细胞类似的原因和内皮特征,调查动脉瘤型络合物形状损伤形式的假设。为了诱导PAH,用SUGEN5416注射大鼠,并暴露于缺氧(10%O_2)3天(早期)或3周(中阶段),或3周的缺氧,另外10周的常氧(晚)阶段pah)。我们在PAH和正常大鼠肺部序列部分中检查了肺脉管系统和血管重塑的形态。形成在肺动脉小侧分支的动脉瘤型络合物,其形态学特性类似于占式动脉。在PAH的发展过程中,小肺动脉的KI67阳性细胞数量增加,包括上列动脉,而大量肺动脉均持续低位。与小型肺动脉相比,在上列动脉中延迟了Ki67阳性细胞的增加。在晚期PAH中,可能是占星动脉的小型非传统侧分支的-90%几乎关闭。这些结果支持我们的假设,以至于,占星术是Sugen5416 /缺氧/常氧暴露的PAH大鼠动脉瘤型丛状病灶的主要部位,部分原因是它们独特的解剖学性质和内皮细胞的过增殖潜力的组合。我们提出,宿主中延迟和广泛的闭塞性病变形成可以是PAH患者的预防治疗靶标。

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