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首页> 外文期刊>The Journal of Nutritional Biochemistry >High fat diet-induced animal model of age-associated obesity and osteoporosis.
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High fat diet-induced animal model of age-associated obesity and osteoporosis.

机译:高脂饮食诱发的年龄相关性肥胖和骨质疏松症动物模型。

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Osteoporosis and obesity remain a major public health concern through its associated fragility and fractures. Several animal models for the study of osteoporotic bone loss, such as ovariectomy (OVX) and denervation, require unique surgical skills and expensive set up. The challenging aspect of these age-associated diseases is that no single animal model exactly mimics the progression of these human-specific chronic conditions. Accordingly, to develop a simple and novel model of post menopausal bone loss with obesity, we fed either a high fat diet containing 10% corn oil (CO) or standard rodent lab chow (LC) to 12-month-old female C57Bl/6J mice for 6 months. As a result, CO fed mice exhibited increased body weight, total body fat mass, abdominal fat mass and reduced bone mineral density (BMD) in different skeletal sites measured by dual energy X-ray absorptiometry. We also observed that decreased BMD with age in CO fed obese mice was accompanied by increased bone marrow adiposity, up-regulation of peroxisome proliferator-activated receptor gamma, cathepsin k and increased proinflammatory cytokines (interleukin 6 and tumor necrosis factor alpha) in bone marrow and splenocytes, when compared to that of LC fed mice. Therefore, this appears to be a simple, novel and convenient age-associated model of post menopausal bone loss, in conjunction with obesity, which can be used in pre-clinical drug discovery to screen new therapeutic drugs or dietary interventions for the treatment of obesity and osteoporosis in the human population.
机译:骨质疏松症和肥胖症由于其相关的脆弱性和骨折而仍然是主要的公共卫生问题。用于研究骨质疏松性骨丢失的几种动物模型,例如卵巢切除术(OVX)和去神经支配,需要独特的手术技巧和昂贵的设备。这些与年龄有关的疾病具有挑战性的方面是,没有任何一种动物模型能够准确地模仿这些人类特异性慢性病的进展。因此,为建立一个更简单,更新颖的肥胖型绝经后骨质疏松模型,我们向12月龄的雌性C57Bl / 6J喂了含10%玉米油(CO)或标准啮齿动物实验室食物(LC)的高脂饮食小鼠6个月。结果,用双能X射线吸收法测定,用CO喂养的小鼠在不同骨骼部位显示出体重增加,身体总脂肪量,腹部脂肪量减少和骨矿物质密度(BMD)降低。我们还观察到,用CO喂养的肥胖小鼠的BMD随着年龄的增长而降低,同时伴有骨髓脂肪增多,过氧化物酶体增殖物激活受体γ,组织蛋白酶k上调以及骨髓中促炎细胞因子(白介素6和肿瘤坏死因子α)的增加。与饲喂LC的小鼠相比,脾细胞和脾细胞都好。因此,这似乎是绝经后骨质疏松与肥胖症相关的简单,新颖和方便的年龄相关模型,可用于临床前药物发现,以筛选用于治疗肥胖症的新治疗药物或饮食干预措施和人口中的骨质疏松症。

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