Aging and Metabolism Research Program, Oklahoma Medical Research Foundation (OMRF), Oklahoma City, OK 73104, USA; Reynolds Oklahoma Center on Aging and Departments of Biochemistry and Molecular Biology, Physiology, and Geriatric Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Aging and Metabolism Research Program, Oklahoma Medical Research Foundation (OMRF), Oklahoma City, OK 73104, USA.
J Sport Health Sci. 2020 Mar;9(2):119-131. doi: 10.1016/j.jshs.2019.05.008. Epub 2019 May 24.
Obesity increases knee osteoarthritis (OA) risk through metabolic, inflammatory, and biomechanical factors, but how these systemic and local mediators interact to drive OA pathology is not well understood. We tested the effect of voluntary running exercise after chronic diet-induced obesity on knee OA-related cartilage and bone pathology in mice. We then used a correlation-based network analysis to identify systemic and local factors associated with early-stage knee OA phenotypes among the different diet and exercise groups.
Male C57BL/6J mice were fed a defined control (10% kcal fat) or high fat (HF) (60% kcal fat) diet from 6 to 37 weeks of age. At 25 weeks, one-half of the mice from each diet group were housed in cages with running wheels for the remainder of the study. Histology, micro computed tomography, and magnetic resonance imaging were used to evaluate changes in joint tissue structure and OA pathology. These local variables were then compared to systemic metabolic (body mass, body fat, and glucose tolerance), inflammatory (serum adipokines and inflammatory mediators), and functional (mechanical tactile sensitivity and grip strength) outcomes using a correlation-based network analysis. Diet and exercise effects were evaluated by two-way analysis of variance.
An HF diet increased the infrapatellar fat pad size and posterior joint osteophytes, and wheel running primarily altered the subchondral cortical and trabecular bone. Neither HF diet nor exercise altered average knee cartilage OA scores compared to control groups. However, the coefficient of variation was ≥25% for many outcomes, and some mice in both diet groups developed moderate OA (≥33% maximum score). This supported using correlation-based network analyses to identify systemic and local factors associated with early-stage knee OA phenotypes. In wheel-running cohorts, an HF diet reduced the network size compared to the control diet group despite similar running distances, suggesting that diet-induced obesity dampens the effects of exercise on systemic and local OA-related factors. Each of the 4 diet and activity groups showed mostly unique networks of local and systemic factors correlated with early-stage knee OA.
Despite minimal group-level effects of chronic diet-induced obesity and voluntary wheel running on knee OA pathology under the current test durations, diet and exercise substantially altered the relationships among systemic and local variables associated with early-stage knee OA. These results suggest that distinct pre-OA phenotypes may exist prior to the development of disease.
肥胖通过代谢、炎症和生物力学因素增加膝骨关节炎(OA)的风险,但这些系统性和局部介质如何相互作用以驱动 OA 病理学尚不清楚。我们测试了慢性饮食诱导肥胖后自愿跑步运动对小鼠膝关节 OA 相关软骨和骨病理学的影响。然后,我们使用基于相关性的网络分析来确定不同饮食和运动组中与早期膝关节 OA 表型相关的系统性和局部因素。
雄性 C57BL/6J 小鼠从 6 至 37 周龄喂食特定对照(10%热量脂肪)或高脂肪(HF)(60%热量脂肪)饮食。在 25 周时,每个饮食组的一半小鼠被安置在带有跑步轮的笼子中进行研究的其余部分。使用组织学、微计算机断层扫描和磁共振成像来评估关节组织结构和 OA 病理学的变化。然后,使用基于相关性的网络分析将这些局部变量与系统性代谢(体重、体脂肪和葡萄糖耐量)、炎症(血清脂肪因子和炎症介质)和功能(机械触觉敏感性和握力)结果进行比较。通过双因素方差分析评估饮食和运动的影响。
HF 饮食增加了髌下脂肪垫的大小和关节后骨赘,而跑步轮主要改变了软骨下皮质和小梁骨。与对照组相比,HF 饮食或运动均未改变平均膝关节软骨 OA 评分。然而,许多结果的变异系数≥25%,并且两个饮食组中的一些小鼠都发展为中度 OA(≥33%最大评分)。这支持使用基于相关性的网络分析来确定与早期膝关节 OA 表型相关的系统性和局部因素。在跑步轮组中,尽管跑步距离相似,但 HF 饮食导致网络大小小于对照饮食组,这表明饮食诱导的肥胖削弱了运动对系统性和局部 OA 相关因素的影响。每组饮食和活动都显示了与早期膝关节 OA 相关的局部和系统性因素的独特网络。
尽管在当前测试持续时间下慢性饮食诱导肥胖和自愿跑步对膝关节 OA 病理学的组间影响很小,但饮食和运动极大地改变了与早期膝关节 OA 相关的系统性和局部变量之间的关系。这些结果表明,在疾病发生之前可能存在不同的前 OA 表型。