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首页> 外文期刊>Osteoarthritis and cartilage >Perturbations in the HDL metabolic pathway predispose to the development of osteoarthritis in mice following long-term exposure to western-type diet
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Perturbations in the HDL metabolic pathway predispose to the development of osteoarthritis in mice following long-term exposure to western-type diet

机译:长期接触西式饮食后,HDL代谢途径的紊乱易诱发小鼠骨关节炎的发展

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摘要

Objective: Recent data suggest that obesity and related metabolic aberrations are associated with osteoarthritis (OA) development, a phenomenon that is attributed at least in part to the consumption of lipid-rich diets. To date, the molecular mechanisms that govern the lipid-OA connection remain largely unknown. Given the important role of high-density lipoprotein (HDL) in plasma and tissue lipid metabolism, the main purpose of the present study was to investigate the role of HDL metabolism in the pathobiology of OA. Methods: We used apolipoprotein A-I (apoA-I)-/- mice that lack classical apoA-I containing HDL, LCAT-/- mice that have only immature HDL and relatively reduced HDL-cholesterol levels and control C57BL/6 mice. Mice were placed on chow or western-type (WTD) and monitored for 24 weeks. Knee joints were removed and articular cartilage was isolated for further analyses. Results: The LCAT-/- mice were significantly more sensitive to the development of diet-induced obesity compared to the C57BL/6 and apoA-I-/- mice. Morphological, biochemical and molecular analyses revealed that the LCAT-/- obese mice developed OA, while the C57BL/6 mice that were fed WTD did not. Notably, apoA-I-/- mice that received WTD also developed OA although their body-weight gain was similar to their wild-type counterparts. Interestingly, bone marrow from LCAT-/- and apoA-I-/- mice contained significantly increased number of adipocytes, compared to the other groups. Conclusions: Our findings suggest that perturbations in HDL metabolism predispose to OA following chronic insult with WTD and raise the challenging possibility that HDL has a causative relation to OA in patients with metabolic syndrome. ? 2012 Osteoarthritis Research Society International.
机译:目的:最新数据表明,肥胖症和相关的代谢异常与骨关节炎(OA)的发展有关,这种现象至少部分归因于食用富含脂质的饮食。迄今为止,控制脂质-OA连接的分子机制仍是未知的。鉴于高密度脂蛋白(HDL)在血浆和组织脂质代谢中的重要作用,本研究的主要目的是研究HDL代谢在OA病理学中的作用。方法:我们使用了缺乏经典的含apoA-I的HDL的载脂蛋白A-I(apoA-I)-/-小鼠,仅具有不成熟的HDL和相对降低的HDL-胆固醇水平的LCAT-/-小鼠以及对照组C57BL / 6小鼠。将小鼠置于食物或西部型(WTD)上并监测24周。去除膝关节,分离关节软骨以进行进​​一步分析。结果:与C57BL / 6和apoA-I-/-小鼠相比,LCAT-/-小鼠对饮食诱导的肥胖的发展更加敏感。形态,生化和分子分析表明,LCAT-/-肥胖小鼠发展为OA,而喂食WTD的C57BL / 6小鼠则没有。值得注意的是,接受WTD的apoA-I-/-小鼠也出现了OA,尽管它们的体重增加与野生型相似。有趣的是,与其他组相比,来自LCAT-/-和apoA-I-/-小鼠的骨髓中脂肪细胞的数量明显增加。结论:我们的发现表明,长期感染WTD后,HDL代谢紊乱易患OA,并增加了HDL与代谢综合征患者与OA之间存在因果关系的挑战性可能性。 ? 2012年国际骨关节炎研究学会。

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