MODELING OF MICE AS TEST ANIMALS FOR A PRECLINICAL STUDY OF HYPOLIPIDEMIC AGENTS

Setiyo Budi Santoso, Widarika Santi Hapsari, Renny Setyowati
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Abstract

Animal models suitable for preclinical research are necessary for the discovery of hypolipidemic agents. Various publications have presented alternative dyslipidemia animal models, but identifying a feasible and stable method would serve as a solid reference for researchers. This investigation aimed to establish a sustained dyslipidemia induction that persists after several days of intervention with a hypolipidemic agent. Six groups of mice, each consisting of five primary test animals and one reserve test animal, were used. After a seven-day acclimatization period, we induced each group for 14 days using three different methods: (1) 5% body weight of quail egg yolks (5% QEY), (2) 10% body weight of used cooking oil (10% UCOs), and (3) a combination of 5% QEY and 10% UCOs. Once all mice reached their peak lipid levels, we evaluated lipid performance through a seven-day intervention with simvastatin (0.026 mg/20-gram body weight) in one of the paired groups. A 14-day combined induction of 5% QEY and 10% UCOs resulted in a 39% elevation in mouse lipids compared to baseline levels. Our findings offer an alternative to traditional dyslipidemia models. However, the development of an animal model for dyslipidemia still poses challenges. Therefore, the identification of novel biomarkers capable of targeting dyslipidemia in humans is crucial.
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建立小鼠模型作为临床前研究降血脂药物的实验动物
适合临床前研究的动物模型是发现降血脂药物的必要条件。各种出版物已经提出了其他血脂异常动物模型,但确定一种可行且稳定的方法将为研究人员提供坚实的参考。本研究旨在建立一种持续的诱导血脂异常,持续数天的干预降脂剂。采用6组小鼠,每组5只主要实验动物和1只备用实验动物。经过7 d的驯化,每组采用3种不同的诱导方法(1)5%体重的鹌鹑蛋黄(5% QEY),(2) 10%体重的废食用油(10% UCOs), (3) 5% QEY和10% UCOs的组合诱导,每组诱导14 d。一旦所有小鼠达到其脂质峰值水平,我们通过对其中一组进行为期7天的辛伐他汀(0.026 mg/20克体重)干预来评估脂质表现。在14天的联合诱导下,5%的QEY和10%的UCOs导致小鼠脂质较基线水平升高39%。我们的发现为传统的血脂异常模型提供了另一种选择。然而,血脂异常动物模型的开发仍然面临挑战。因此,鉴定能够靶向人类血脂异常的新型生物标志物至关重要。
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0.00%
发文量
70
审稿时长
12 weeks
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