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Confirmation of the guinea pig as an experimental model of inflammation with dietary-induced atherosclerosis.

机译:确认豚鼠为饮食诱发的动脉粥样硬化炎症的实验模型。

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Inflammation plays a major role in the development of atherosclerotic vascular disease through its diverse affects on arterial wall biology and lipoprotein metabolism. Inflammatory cells are a prominent feature of atherosclerotic lesions, both in humans and cholesterol-fed animal models of atherosclerosis. Given the critical nature of inflammation, an ideal animal model of atherosclerosis should have a resemblance to the human disease in terms of both cholesterol and lipoprotein metabolism and the inflammatory process. The primary aim of this study was to develop the guinea pig as an experimental animal model of inflammation in dietary-induced atherosclerosis. A secondary aim was to compare the effects of a high-cholesterol diet either high or low in carbohydrate on inflammatory markers. Thirty male Hartley guinea pigs were randomly assigned to one of three diet treatments for 12 wk (Low-Cholesterol, High-Cholesterol/High-Carbohydrate and High-Cholesterol/Low-Carbohydrate Groups). Animals were euthanized after 12 weeks and blood samples taken for determination of plasma lipids and serum total ketone bodies. The aorta was dissected and separated into three sections for measurement of cytokine protein concentrations (INF-gamma, TNF-alpha, IL-1beta, IL-6 and GM-CSF), mRNA expression (IFN-gamma, TNF-alpha, IL-1beta, MCP-1 and IL-8) and cholesterol concentration in the aorta. There was a significant increase in all cytokine protein concentrations in the high-cholesterol/high-carbohydrate group compared to the low-cholesterol group. The high-cholesterol/low-carbohydrate group also demonstrated a significant increase in all cytokine protein concentrations except GM-CSF. Real-time RT-PCR showed a significant increase in the expression of IFN-gamma and TNF-alpha mRNA for both high-cholesterol groups compared to the low-cholesterol group. This study is the first to confirm that guinea pigs do demonstrate an increased vascular inflammatory response after the intake of an atherogenic diet. This novel finding is important as it will allow for the use of guinea pigs in future studies by where a system-wide animal model can be evaluated for the cellular and molecular components involved in the immunomodulation of atherosclerosis.
机译:炎症通过对动脉壁生物学和脂蛋白代谢的多种影响,在动脉粥样硬化性血管疾病的发展中起主要作用。在人类和胆固醇喂养的动脉粥样硬化动物模型中,炎症细胞都是动脉粥样硬化病变的突出特征。考虑到炎症的关键性质,理想的动脉粥样硬化动物模型在胆固醇和脂蛋白代谢以及炎症过程方面应与人类疾病相似。这项研究的主要目的是开发豚鼠作为饮食诱导的动脉粥样硬化炎症的实验动物模型。第二个目的是比较高胆固醇饮食(碳水化合物含量高或低)对炎症指标的影响。将30只雄性Hartley豚鼠随机分配到三种饮食疗法中,每周12周(低胆固醇,高胆固醇/高碳水化合物和高胆固醇/低碳水化合物组)之一。 12周后对动物实施安乐死,并采集血样以确定血浆脂质和血清总酮体。将主动脉解剖并分成三部分,以测量细胞因子蛋白浓度(INF-γ,TNF-α,IL-1β,IL-6和GM-CSF),mRNA表达(IFN-γ,TNF-α,IL- 1beta,MCP-1和IL-8)和主动脉中的胆固醇浓度。与低胆固醇组相比,高胆固醇/高碳水化合物组的所有细胞因子蛋白浓度均显着增加。高胆固醇/低碳水化合物组还显示除GM-CSF外所有细胞因子蛋白浓度均显着增加。实时RT-PCR显示,与低胆固醇组相比,两个高胆固醇组的IFN-γ和TNF-αmRNA的表达均显着增加。这项研究是第一个证实豚鼠在摄取致动脉粥样化饮食后确实表现出血管炎性反应增强的研究。这一新发现很重要,因为它将允许在以后的研究中使用豚鼠,通过该动物可以评估全系统动物模型中涉及动脉粥样硬化免疫调节的细胞和分子成分。

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