McGrath Cody, Sankaran Jeyantt S, Misaghian-Xanthos Negin, Sen Buer, Xie Zhihui, Styner Martin A, Zong Xiaopeng, Rubin Janet, Styner Maya
Department of Medicine, Division of Endocrinology, University of North Carolina, Chapel Hill, NC, USA.
Department of Computer Science, University of North Carolina, Chapel Hill, NC, USA.
J Bone Miner Res. 2020 Jan;35(1):106-115. doi: 10.1002/jbmr.3872. Epub 2019 Oct 25.
Marrow adipose tissue (MAT) and its relevance to skeletal health during caloric restriction (CR) is unknown: It remains unclear whether exercise, which is anabolic to bone in a calorie-replete state, alters bone or MAT in CR. We hypothesized that response of bone and MAT to exercise in CR differs from the calorie-replete state. Ten-week-old female B6 mice fed a regular diet (RD) or 30% CR diet were allocated to sedentary (RD, CR, n = 10/group) or running exercise (RD-E, CR-E, n = 7/group). After 6 weeks, CR mice weighed 20% less than RD, p < 0.001; exercise did not affect weight. Femoral bone volume (BV) via 3D MRI was 20% lower in CR versus RD (p < 0.0001). CR was associated with decreased bone by μCT: Tb.Th was 16% less in CR versus RD, p < 0.003, Ct.Th was 5% less, p < 0.07. In CR-E, Tb.Th was 40% less than RD-E, p < 0.0001. Exercise increased Tb.Th in RD (+23% RD-E versus RD, p < 0.003) but failed to do so in CR. Cortical porosity increased after exercise in CR (+28%, p = 0.04), suggesting exercise during CR is deleterious to bone. In terms of bone fat, metaphyseal MAT/ BV rose 159% in CR versus RD, p = 0.003 via 3D MRI. Exercise decreased MAT/BV by 52% in RD, p < 0.05, and also suppressed MAT in CR (-121%, p = 0.047). Histomorphometric analysis of adipocyte area correlated with MAT by MRI (R = 0.6233, p < 0.0001). With respect to bone, TRAP and Sost mRNA were reduced in CR. Intriguingly, the repressed Sost in CR rose with exercise and may underlie the failure of CR-bone quantity to increase in response to exercise. Notably, CD36, a marker of fatty acid uptake, rose 4088% in CR (p < 0.01 versus RD), suggesting that basal increases in MAT during calorie restriction serve to supply local energy needs and are depleted during exercise with a negative impact on bone. © 2019 The Authors. Journal of Bone and Mineral Research published by American Society for Bone and Mineral Research.
骨髓脂肪组织(MAT)及其在热量限制(CR)期间与骨骼健康的相关性尚不清楚:目前仍不清楚在热量充足状态下对骨骼具有合成代谢作用的运动,在CR期间是否会改变骨骼或MAT。我们假设CR期间骨骼和MAT对运动的反应与热量充足状态不同。将10周龄雌性B6小鼠分为正常饮食(RD)组或30%CR饮食组,每组再分为久坐组(RD、CR,每组n = 10)或跑步运动组(RD-E、CR-E,每组n = 7)。6周后,CR小鼠体重比RD小鼠轻20%,p < 0.001;运动对体重无影响。通过三维磁共振成像(3D MRI)测量,CR组股骨骨体积(BV)比RD组低20%(p < 0.0001)。μCT显示CR与骨量减少有关:与RD组相比,CR组骨小梁厚度(Tb.Th)减少16%,p < 0.003,皮质厚度(Ct.Th)减少5%,p < 0.07。在CR-E组中,Tb.Th比RD-E组减少40%,p < 0.0001。运动使RD组的Tb.Th增加(RD-E组比RD组增加23%,p < 0.003),但在CR组中未能增加。CR组运动后皮质骨孔隙率增加(+28%,p = 0.04),表明CR期间运动对骨骼有害。在骨脂肪方面,通过3D MRI测量,CR组干骺端MAT/BV比RD组增加159%,p = 0.003。运动使RD组的MAT/BV降低52%,p < 0.05,在CR组中也抑制了MAT(-121%,p = 0.047)。脂肪细胞面积的组织形态计量学分析与MRI测量的MAT相关(R = 0.6233,p < 0.0001)。在骨骼方面,CR组中抗酒石酸酸性磷酸酶(TRAP)和硬化蛋白(Sost)mRNA水平降低。有趣的是,CR组中受抑制的Sost随着运动而升高,这可能是CR组骨量未能因运动而增加的原因。值得注意的是,脂肪酸摄取标志物CD36在CR组中升高了4088%(与RD组相比,p < 0.01),这表明热量限制期间MAT的基础增加有助于满足局部能量需求,而在运动期间会被消耗,对骨骼产生负面影响。© 2019作者。《骨与矿物质研究杂志》由美国骨与矿物质研究学会出版。