A novel rat model of fatty organ degeneration induced by poloxamer 407

Na Yin, Ting Chu, Yin Peng, Yuanchun Yao, Jingjing Li, B. Xiang, Bo Yang, T. Johnston, Maosheng Yang
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Abstract

Abstract Traditional methods of inducing hyperlipidemia in animal models are either costly (genetic manipulation) or it is difficult to control for the effects of other variables. For example, during high-fat feeding, the amount of high-fat diet intake per animal cannot be precisely controlled. The aim of this study was to develop an experimental model of fatty organ degeneration induced by poloxamer 407 (P-407). The study was conducted in 2-month-old, male Sprague-Dawley rats that were administered intraperitoneally with either 10% (w/w) P-407 (1 g/kg) or saline (10 mL/kg) for 4 months. Their lipid profile, organ degeneration due to fat deposition, and body mass were assessed. Intraperitoneal administration of P-407 resulted in significant increases in plasma triglycerides (P ⩽ 0.001), total cholesterol (P < 0.001), high-density lipoprotein-cholesterol (P ⩽ 0.001), and low-density lipoprotein (P < 0.001) cholesterol. In contrast to the control group, fatty tissue degeneration was observed in the liver, spleen, and kidneys of P-407-treated rats. Positive correlations between fatty tissue degeneration, and the atherogenic index of plasma (P < 0.001) and the ratio of total cholesterol to high-density-lipoprotein (P < 0.001) were identified. In addition, treatment with P-407 for 3 to 4 months caused a significant reduction in body mass relative to controls (P < 0.001). Thus, this study describes the development of a cost-effective experimental rat model of organ degeneration, characterized by fat accumulation in the liver, spleen, and kidneys, which could be used for the study of steatosis and related diseases arising from sustained untreated dyslipidemia. Furthermore, both the atherogenic index of plasma and the ratio of total cholesterol to high-density lipoprotein-cholesterol can be used to predict the risk of fatty tissue degeneration in this model. The study was approval of the University of Jishou Biomedical Research Ethics Committee, China.
波洛沙姆407致大鼠脂肪器官变性的新模型
在动物模型中诱导高脂血症的传统方法要么成本高(基因操作),要么难以控制其他变量的影响。例如,在高脂肪饲养过程中,每只动物的高脂肪饲料摄取量无法精确控制。本研究的目的是建立波洛沙姆407 (P-407)致脂肪器官变性的实验模型。该研究在2个月大的雄性Sprague-Dawley大鼠中进行,腹腔注射10% (w/w) P-407 (1 g/kg)或生理盐水(10 mL/kg) 4个月。评估了他们的脂质谱、脂肪沉积引起的器官变性和体重。腹腔注射P-407导致血浆甘油三酯(P < 0.001)、总胆固醇(P < 0.001)、高密度脂蛋白-胆固醇(P < 0.001)和低密度脂蛋白(P < 0.001)胆固醇显著升高。与对照组相比,p -407处理大鼠的肝脏、脾脏和肾脏均出现脂肪组织变性。脂肪组织变性与血浆动脉粥样硬化指数(P < 0.001)和总胆固醇/高密度脂蛋白比值(P < 0.001)呈正相关。此外,与对照组相比,P-407治疗3 -4个月导致体重显著降低(P < 0.001)。因此,本研究描述了一种具有成本效益的器官变性实验大鼠模型的发展,其特征是肝脏、脾脏和肾脏的脂肪积累,可用于研究脂肪变性和持续未经治疗的血脂异常引起的相关疾病。此外,血浆的动脉粥样硬化指数和总胆固醇与高密度脂蛋白-胆固醇的比值都可以用来预测该模型中脂肪组织变性的风险。本研究已获中国吉首大学生物医学研究伦理委员会批准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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