Collins K H, Reimer R A, Seerattan R A, Leonard T R, Herzog W
Human Performance Laboratory, University of Calgary, AB, Canada; McCaig Institute for Bone and Joint Health, University of Calgary, AB, Canada.
Human Performance Laboratory, University of Calgary, AB, Canada; Department of Biochemistry and Molecular Biology, University of Calgary, AB, Canada.
Osteoarthritis Cartilage. 2015 Jun;23(6):957-65. doi: 10.1016/j.joca.2015.01.015. Epub 2015 Feb 3.
Osteoarthritis (OA) in obese individuals is often attributed to joint loading. However, a subtype of OA, Metabolic OA, may be due to obesity-related intrinsic factors but remains to be evaluated experimentally against a known OA progression model.
To evaluate if obesity contributes to OA onset using a high fat/high sucrose diet-induced obesity (DIO) model with anterior cruciate ligament-transected rats (ACL-X).
Sprague Dawley rats (n = 33) consumed high fat/high sucrose or chow diets for 12 weeks, were randomized to one of three groups: a unilateral ACL-X group, sham surgery group, or naïve non-surgical group. These animals were followed for an additional 16 weeks. At sacrifice, body composition, knee joint Modified Mankin scores, and 27 serum and synovial fluid cytokines and adipokines were measured.
Experimental limbs of obese ACL-X, obese Sham, and lean ACL-X animals had similar Modified Mankin scores that were greater than those obtained from lean Sham and naïve animals. Obese contralateral limbs had similar OA damage as ACL-X and Sham limbs of obese and ACL-X limbs of lean animals. Obese contralateral limb Modified Mankin scores had a strong correlation (r = 0.75, P < 0.001) with body fat percentage. Serum leptin and synovial fluid IP10/CXCL10 best described Modified Mankin scores in contralateral limbs of obese animals.
Mechanical factors produced OA damage in experimental limbs, as expected. Interestingly, OA damage in obese contralateral limbs was similar to mechanically perturbed limbs, suggesting that obesity may induce OA in a non-mechanical manner.
肥胖个体的骨关节炎(OA)通常归因于关节负荷。然而,OA的一种亚型,即代谢性OA,可能是由肥胖相关的内在因素引起的,但仍有待根据已知的OA进展模型进行实验评估。
使用高脂/高糖饮食诱导肥胖(DIO)模型和前交叉韧带切断大鼠(ACL-X)来评估肥胖是否会导致OA发病。
33只Sprague Dawley大鼠食用高脂/高糖或普通饮食12周,然后随机分为三组之一:单侧ACL-X组、假手术组或未手术的单纯组。这些动物再随访16周。处死时,测量身体成分、膝关节改良曼金评分以及27种血清和滑液细胞因子及脂肪因子。
肥胖ACL-X组、肥胖假手术组和瘦ACL-X组动物的实验肢体具有相似的改良曼金评分,且高于瘦假手术组和未手术单纯组动物。肥胖对侧肢体的OA损伤与肥胖动物的ACL-X和假手术肢体以及瘦动物的ACL-X肢体相似。肥胖对侧肢体改良曼金评分与体脂百分比具有强相关性(r = 0.75,P < 0.001)。血清瘦素和滑液IP10/CXCL10最能描述肥胖动物对侧肢体的改良曼金评分。
正如预期的那样,机械因素在实验肢体中造成了OA损伤。有趣的是,肥胖对侧肢体的OA损伤与机械扰动肢体相似,这表明肥胖可能以非机械方式诱发OA。