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Short-Term Increased Physical Activity During Early Life Affects High-Fat Diet–Induced Bone Loss in Young Adult Mice

机译:早期生命期间的短期增加的身体活动会影响年轻成年小鼠的高脂饮食诱导的骨质损失

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Mechanical stresses associated with physical activity (PA) have beneficial effects on increasing BMD and improving bone quality. However, a high-fat diet (HFD) and obesity tend to have negative effects on bone, by increasing bone marrow adiposity leading to increased excretion of proinflammatory cytokines, which activate RANKL-induced bone resorption. In the current study, whether short-term increased PA via access to voluntary wheel running during early life has persistent and protective effects on HFD-induced bone resorption was investigated. Sixty 4-week-old male C57BL6/J mice were divided into two groups postweaning: without or with PA (access to voluntary running wheel 7–8?km/day) for 4?weeks. After 4?weeks with or without PA, mice were further subdivided into control diet or HFD groups for 8?weeks, and then all animals were switched back to control diet for an additional 4?weeks. Mice from the HFD groups were significantly heavier and obese; however, after 4?weeks of additional control diet their body weights returned to levels of mice on continuous control diet. Using μ-CT and confirmed by pQCT of tibias and spines ex vivo, it was determined that bone volume and trabecular BMD were significantly increased with PA in control diet animals compared with sedentary animals without access to wheels, and such anabolic effects of PA on bone were sustained after ceasing PA in adult mice. Eight weeks of a HFD deteriorated bone development in mice. Unexpectedly, early-life PA did not prevent persistent effects of HFD on deteriorating bone quality; in fact, it exacerbated a HFD-induced inflammation, osteoclastogenesis, and trabecular bone loss in adult mice. In accordance with these data, signal transduction studies revealed that a HFD-induced Ezh2, DNA methyltransferase 3a, and nuclear factor of activated T-cells 1 expression were amplified in nonadherent hematopoietic cells. In conclusion, short-term increased PA in early life is capable of increasing bone mass; however, it alters the HFD-induced bone marrow hematopoietic cell-differentiation program to exacerbate increased bone resorption if PA is halted. ? 2021 Arkansas Children's Nutrition Center. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
机译:与物理活性(PA)相关的机械应力对增加BMD和改善骨质质量有益的影响。然而,通过增加骨髓肥胖导致促炎细胞因子的排泄增加的骨髓肥胖,它倾向于对骨骼产生负面影响的高脂饮食(HFD)和肥胖趋于对骨骼产生负面影响。在目前的研究中,是否通过早期生命期间通过志愿车轮进行短期增加的PA,对HFD诱导的骨吸收进行了持续和保护作用。六十四周雄性C57BL6 / J小鼠分为两组后切换:没有或PA(访问自愿运行轮7-8?KM /日)4?周。在4个?有或没有PA的周后,小鼠进一步细分为控制饮食或HFD组8?周,然后将所有动物切换回控制饮食另外4个时间。来自HFD组的小鼠显着较重和肥胖;然而,在4个?几周的额外控制饮食后,他们的体重恢复到连续对照饮食中的小鼠水平。使用μ-CT并通过胫骨的PQCT证实,并确定骨体积和小梁BMD与久入动物的PA与久坐动植物相比显着增加,无需轮子,以及PA在骨骼上的这种合成代谢效应在成人小鼠中停止PA后持续。八十周的氢乳头在小鼠中骨骼发育劣化。出乎意料的是,早期PA并没有阻止HFD对骨质质量恶化的持续影响;事实上,它加剧了成年小鼠的HFD诱导的炎症,骨质细胞发生和小梁骨质损失。根据这些数据,信号转导研究表明,在非相继的造血细胞中扩增了HFD诱导的EZH2,DNA甲基转移酶3a和活化T细胞1表达的核因子。总之,早期生命中的短期增加了PA能够增加骨量;然而,如果PA停止,它会改变HFD诱导的骨髓造血细胞分化计划以加剧骨吸收增加。还2021年阿肯色州儿童营养中心。 JBMR Plus由Wiley Moustiongs LLC发布代表美国骨骼和矿物学研究。

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