Avia Paz, Kareem Midlej, Osayd Zohud, Iqbal M. Lone, Fuad A. Iraqi
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The CC mice are a genetically diverse panel derived from eight inbred strains.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Our findings demonstrated significant variations in the recorded phenotypes across different CC lines compared to the reference mouse line, C57BL/6J. CC037 line exhibited a substantial increase in body weight on HFD, whereas line CC005 exhibited differing responses based on sex. Glucose tolerance tests revealed significant variations, with some lines like CC005 showing a marked increase in area under the curve (AUC) values on HFD. Organ weights, including brain, spleen, liver, and kidney, varied significantly among the lines and sexes in response to HFD. Behavioral tests using the Morris water maze indicated that cognitive performance was differentially affected by diet and genetic background.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>Our study establishes a foundation for future quantitative trait loci mapping using CC lines and identifying genes underlying the comorbidity of Alzheimer's disease (AD), caused by obesity and T2D. The genetic components may offer new tools for early prediction and prevention.</p>\n </section>\n </div>","PeriodicalId":93869,"journal":{"name":"Animal models and experimental medicine","volume":"8 1","pages":"126-141"},"PeriodicalIF":0.0000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ame2.12488","citationCount":"0","resultStr":"{\"title\":\"The collaborative cross mouse for studying the effect of host genetic background on memory impairments due to obesity and diabetes\",\"authors\":\"Avia Paz, Kareem Midlej, Osayd Zohud, Iqbal M. Lone, Fuad A. Iraqi\",\"doi\":\"10.1002/ame2.12488\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Over the past few decades, a threefold increase in obesity and type 2 diabetes (T2D) has placed a heavy burden on the health-care system and society. 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引用次数: 0
摘要
背景:在过去几十年里,肥胖症和 2 型糖尿病(T2D)患者增加了三倍,给医疗保健系统和社会带来了沉重负担。以往的研究表明,肥胖、T2D 和神经退行性疾病(包括痴呆症)之间存在相关性。当务之急是进一步了解肥胖、T2D 和认知障碍之间的关系:本研究测试并评估了高脂饮食(HFD)诱导的肥胖和T2D对认知能力的影响,以及宿主遗传背景对合作杂交(CC)小鼠因肥胖和T2D导致认知能力下降严重程度的影响。CC小鼠是由8个近交系小鼠组成的遗传多样性小组:结果:我们的研究结果表明,与参考小鼠品系 C57BL/6J 相比,不同 CC 品系记录的表型存在明显差异。CC037品系在高密度脂蛋白膳食中体重大幅增加,而CC005品系则根据性别表现出不同的反应。葡萄糖耐量测试显示出明显的差异,一些品系(如 CC005)在高密度脂蛋白饲料中的曲线下面积(AUC)值明显增加。器官重量(包括脑、脾脏、肝脏和肾脏)在不同品系和性别对高氟日粮的反应中存在显著差异。使用莫里斯水迷宫进行的行为测试表明,认知能力受到饮食和遗传背景的不同影响:结论:我们的研究为今后利用 CC 株系绘制数量性状位点图和鉴定肥胖与 T2D 导致的阿尔茨海默病(AD)并发症的潜在基因奠定了基础。这些基因成分可为早期预测和预防提供新的工具。
The collaborative cross mouse for studying the effect of host genetic background on memory impairments due to obesity and diabetes
Background
Over the past few decades, a threefold increase in obesity and type 2 diabetes (T2D) has placed a heavy burden on the health-care system and society. Previous studies have shown correlations between obesity, T2D, and neurodegenerative diseases, including dementia. It is imperative to further understand the relationship between obesity, T2D, and cognitive deficits.
Methods
This investigation tested and evaluated the cognitive impact of obesity and T2D induced by high-fat diet (HFD) and the effect of the host genetic background on the severity of cognitive decline caused by obesity and T2D in collaborative cross (CC) mice. The CC mice are a genetically diverse panel derived from eight inbred strains.
Results
Our findings demonstrated significant variations in the recorded phenotypes across different CC lines compared to the reference mouse line, C57BL/6J. CC037 line exhibited a substantial increase in body weight on HFD, whereas line CC005 exhibited differing responses based on sex. Glucose tolerance tests revealed significant variations, with some lines like CC005 showing a marked increase in area under the curve (AUC) values on HFD. Organ weights, including brain, spleen, liver, and kidney, varied significantly among the lines and sexes in response to HFD. Behavioral tests using the Morris water maze indicated that cognitive performance was differentially affected by diet and genetic background.
Conclusions
Our study establishes a foundation for future quantitative trait loci mapping using CC lines and identifying genes underlying the comorbidity of Alzheimer's disease (AD), caused by obesity and T2D. The genetic components may offer new tools for early prediction and prevention.