首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Dose-related effects of doxazosin on plasma lipids and aortic fatty streak formation in the hypercholesterolemic hamster model.
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Dose-related effects of doxazosin on plasma lipids and aortic fatty streak formation in the hypercholesterolemic hamster model.

机译:在高胆固醇血症仓鼠模型中多沙唑嗪对血浆脂质和主动脉脂肪条纹形成的剂量相关影响。

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摘要

Doxazosin, an alpha 1-adrenergic inhibitor, has been shown to decrease hypertension and plasma lipids, especially total cholesterol (TC) and low-density lipoprotein cholesterol (LDL-C), thus reducing certain risk factors associated with increased incidence of cardiovascular disease. One preliminary report indicated that the decrease in LDL-C in hypercholesterolemic hamsters treated with doxazosin was associated with a reduction in fatty streak formation. However, since the effects of doxazosin on plasma lipids, aortic fatty streak development, or the relationship between the two have not been studied in a dose-dependent manner, these effects were further investigated over varying doses of doxazosin (0, 1, 5, 10, and 20 mg/kg body wt/day) during a 10-week period. Doxazosin administration was associated with a dose-dependent decrease in LDL-C of 2%, 29%, 52%, and 60%, whereas the degree of fatty streak formation was reduced 11%, 45%, 76%, and 92% compared with controls, with the first statistically significant decrease for both parameters at the 10 mg/kg dose. Significant correlations between LDL-C concentrations and fatty streak area suggest that doxazosin altered aortic lipid infiltration primarily by its effect on plasma lipids. However, the 20 mg/kg dose of doxazosin significantly decreased lesion area compared with the 10 mg/kg dose without a further effect on plasma lipid concentrations. Three animals at these higher doses demonstrated no stainable lipid inclusions while maintaining plasma lipid values similar to their cohorts. These exceptions to the lipid-lesion relationship raise the possibility of additional effects of doxazosin, which may occur independent of or in concert with lipoprotein cholesterol lowering, on lesion formation.
机译:多沙唑嗪是一种α1肾上腺素能抑制剂,已显示可降低高血压和血浆脂质,尤其是总胆固醇(TC)和低密度脂蛋白胆固醇(LDL-C),从而降低与心血管疾病发生率增加相关的某些危险因素。一份初步报告表明,用多沙唑嗪处理的高胆固醇仓鼠中LDL-C的减少与脂肪条纹形成的减少有关。但是,由于尚未以剂量依赖性的方式研究多沙唑嗪对血浆脂质,主动脉脂肪条纹形成或两者之间的关系的影响,因此在不同剂量的多沙唑嗪中进一步研究了这些影响(0、1、5, 10和20 mg / kg体重/天),持续10周。多沙唑嗪的给药使LDL-C的剂量依赖性降低分别为2%,29%,52%和60%,而脂肪条纹形成的程度与降低相比降低了11%,45%,76%和92%与对照组相比,在10 mg / kg剂量下,这两个参数的统计上均首次出现显着下降。 LDL-C浓度与脂肪条纹面积之间的显着相关性表明,多沙唑嗪主要通过其对血浆脂质的作用来改变主动脉脂质的浸润。但是,与10 mg / kg剂量相比,20 mg / kg剂量的多沙唑嗪显着降低了病变面积,而对血浆脂质浓度没有进一步影响。在这些较高剂量下的三只动物在保持血浆脂质值与其队列相似的同时,没有显示出可染色的脂质包裹体。这些脂质-病变关系的例外情况增加了多沙唑嗪对病变形成的影响,该作用可能独立于脂蛋白胆固醇降低或与脂蛋白胆固醇降低协同发生。

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