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高龄 C57BL/6JRj 小鼠在西方饮食暴露下不会发生肥胖。

Advanced-age C57BL/6JRj mice do not develop obesity upon western-type diet exposure.

机构信息

a Center for Molecular and Vascular Biology, Department of Cardiovascular Sciences , KU Leuven , Leuven , Belgium.

出版信息

Adipocyte. 2019 Dec;8(1):105-113. doi: 10.1080/21623945.2019.1590893. Epub 2019 Mar 26.

DOI:10.1080/21623945.2019.1590893
PMID:30860940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6768272/
Abstract

Obesity has become a global health-threat for every age group. It is well known that young mice (10-12 weeks of age) fed a western-type diet (WD) become obese and develop higher cholesterol levels and liver steatosis whereas insulin sensitivity is reduced. Less is known, however, about the effect of a WD on advanced-age mice. Therefore, 10 week-old (young) and 22 month-old (advanced-age), male C57BL/6JRj mice were kept on either a WD or a control diet (SFD) for 15 weeks. In contrast to young mice, advanced-age mice on WD did not show a higher body weight or adipose tissue (AT)-masses, suggesting a protection against diet-induced obesity. Furthermore, plasma adiponectin and leptin levels were not affected upon WD-feeding. A WD, however, did induce more hepatic lipid accumulation as well as increased hepatic expression of the macrophage marker F4/80, in advanced-age mice. There were no significant differences in mRNA levels of uncoupling protein-1 or F4/80 in brown AT (BAT) or of several intestinal integrity markers in colon suggesting that the protection against obesity is not due to excessive BAT or to impaired intestinal absorption of fat. Thus, advanced-age mice, in contrast to their younger counterparts, appeared to be protected against diet-induced obesity.

摘要

肥胖已成为全年龄段的全球性健康威胁。众所周知,食用西式饮食(WD)的年轻老鼠(10-12 周龄)会肥胖,并导致胆固醇水平升高和肝脏脂肪变性,而胰岛素敏感性降低。然而,对于 WD 对老年老鼠的影响知之甚少。因此,10 周龄(年轻)和 22 月龄(老年)雄性 C57BL/6JRj 老鼠分别喂食 WD 或对照饮食(SFD)15 周。与年轻老鼠不同,WD 喂养的老年老鼠体重或脂肪组织(AT)质量没有增加,这表明它们对饮食诱导的肥胖具有保护作用。此外,WD 喂养不会影响血浆脂联素和瘦素水平。然而,WD 确实会导致老年老鼠肝脏中脂质积累增加,以及巨噬细胞标志物 F4/80 的肝表达增加。在棕色 AT(BAT)或结肠中几种肠道完整性标志物中,没有观察到解偶联蛋白-1 或 F4/80 的 mRNA 水平有显著差异,这表明对肥胖的保护不是由于 BAT 过度或脂肪吸收受损所致。因此,与年轻老鼠相比,老年老鼠似乎对饮食诱导的肥胖具有保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ecd/6768272/6fdd78d5ea06/kadi-08-01-1590893-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ecd/6768272/a4762c5d9ff4/kadi-08-01-1590893-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ecd/6768272/6fdd78d5ea06/kadi-08-01-1590893-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ecd/6768272/a4762c5d9ff4/kadi-08-01-1590893-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ecd/6768272/6fdd78d5ea06/kadi-08-01-1590893-g002.jpg

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