Chen Jin-Ran, Lazarenko Oxana P, Carvalho Eugenia, Blackburn Michael L, Shankar Kartik, Wankhade Umesh D, Børsheim Elisabet
Arkansas Children's Nutrition Center Little Rock AR USA.
Department of Pediatrics University of Arkansas for Medical Sciences Little Rock AR USA.
JBMR Plus. 2021 May 14;5(7):e10508. doi: 10.1002/jbm4.10508. eCollection 2021 Jul.
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. published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
与体育活动(PA)相关的机械应力对增加骨密度和改善骨质量具有有益作用。然而,高脂饮食(HFD)和肥胖往往对骨骼产生负面影响,通过增加骨髓脂肪量导致促炎细胞因子排泄增加,从而激活RANKL诱导的骨吸收。在本研究中,研究了在生命早期通过自愿轮转跑步短期增加PA是否对HFD诱导的骨吸收具有持续的保护作用。60只4周龄雄性C57BL6/J小鼠在断奶后分为两组:不进行PA组或进行PA组(可自愿使用跑步轮,每天跑7-8公里),持续4周。在有或没有PA的情况下饲养4周后,小鼠进一步分为对照饮食组或HFD组,持续8周,然后所有动物再换回对照饮食,持续4周。HFD组的小鼠明显更重且肥胖;然而,在额外的对照饮食4周后,它们的体重恢复到持续食用对照饮食的小鼠的水平。通过μ-CT并经离体胫骨和脊柱的pQCT证实,与没有使用轮子的久坐动物相比,对照饮食动物中PA显著增加了骨体积和小梁骨密度,并且在成年小鼠停止PA后,PA对骨骼的这种合成代谢作用仍然持续。8周的HFD会使小鼠的骨骼发育恶化。出乎意料的是,生命早期的PA并不能预防HFD对骨骼质量恶化的持续影响;事实上,它加剧了成年小鼠中HFD诱导的炎症、破骨细胞生成和小梁骨丢失。根据这些数据,信号转导研究表明,HFD诱导的Ezh2、DNA甲基转移酶3a和活化T细胞核因子1在非贴壁造血细胞中的表达被放大。总之,生命早期短期增加PA能够增加骨量;然而,如果停止PA,它会改变HFD诱导的骨髓造血细胞分化程序,加剧骨吸收增加。©2021阿肯色儿童营养中心。由Wiley Periodicals LLC代表美国骨与矿物质研究学会出版。