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运动和他汀类药物对大鼠股骨强度的协同作用。

Synergistic effect of exercise and statins on femoral strength in rats.

机构信息

Department of Kinesiology, The University of Texas at Austin, Austin, TX 78712, United States.

出版信息

Exp Gerontol. 2013 Aug;48(8):751-5. doi: 10.1016/j.exger.2013.04.007. Epub 2013 Apr 26.

Abstract

It is now widely recognized that in order to optimize bone health in the later years, bone healthy behaviors should begin at a young age and continue throughout life. Prescribed orally to lower lipid levels in adults of all ages, statins have also been shown to stimulate bone formation in vitro by promoting bone morphogenic protein-2 (BMP-2) activity and to stimulate bone formation in vivo. Weight bearing exercise is well known to stimulate bone formation through a mechanism whereby mechanical loading is 'sensed' by the mechano-sensors leading to a cascade of events involving the activation of osteoblasts. For individuals with high cholesterol levels, both of these interventions are recommended throughout adult life. Since statins and exercise stimulate bone formation via different mechanisms, we hypothesized that exercise in combination with oral simvastatin synergistically increases bone mineral density and strength. Mature adult female, Sprague Dawley rats were divided into 4 groups: control (n=9), statin only (n=8), exercise only (n=11), and statin plus exercise (n=11). Simvastatin was given to the two groups at a dose of 10 mg/kg/day in standard rat chow for the entire 5 week period. All rats ate the same mass of food. The two exercise groups ran on a treadmill with progressively greater speeds and time, ending on week 5 at 30 m/min for 60 min. After 5 weeks, rats were euthanized, and excised femurs were scanned for areal bone mineral density (BMD) and tested by three point bending to obtain the following performance measures: maximum force (strength), stiffness, and work-to-fracture. Only the group treated with statins and exercise showed a positive effect on the biomechanical performance of the femurs. Compared to controls, this group had increased maximum force, stiffness, moment of inertia, and BMD. Linear regression analysis revealed that the increased performance was related to increased BMD. We conclude that the combination of oral statins and appropriate exercise increases bone strength better than either individual treatment and may provide optimal protection against osteoporosis.

摘要

现在人们普遍认识到,为了优化晚年的骨骼健康,骨骼健康的行为应该从年轻时开始,并贯穿一生。他汀类药物被规定用于降低所有年龄段成年人的血脂水平,也已被证明可以通过促进骨形态发生蛋白-2(BMP-2)活性来刺激体外骨形成,并刺激体内骨形成。负重运动通过一种机制众所周知可以刺激骨形成,即机械负荷被机械感受器“感知”,导致涉及成骨细胞激活的级联事件。对于胆固醇水平高的个体,这两种干预措施在整个成年期都被推荐。由于他汀类药物和运动通过不同的机制刺激骨形成,我们假设运动与口服辛伐他汀联合使用会协同增加骨密度和骨强度。成熟的成年雌性 Sprague Dawley 大鼠被分为 4 组:对照组(n=9)、他汀类药物组(n=8)、运动组(n=11)和他汀类药物加运动组(n=11)。辛伐他汀以 10mg/kg/天的剂量添加到标准大鼠饲料中,连续 5 周。所有大鼠都吃相同质量的食物。两组运动大鼠在跑步机上以逐渐增加的速度和时间跑步,在第 5 周结束时以 30m/min 的速度跑 60 分钟。5 周后,大鼠被安乐死,取出股骨进行面积骨密度(BMD)扫描,并通过三点弯曲测试获得以下性能指标:最大力(强度)、刚度和断裂功。只有接受他汀类药物和运动治疗的组对股骨的生物力学性能有积极影响。与对照组相比,该组的最大力、刚度、转动惯量和 BMD 增加。线性回归分析表明,性能的提高与 BMD 的增加有关。我们得出结论,口服他汀类药物和适当运动的结合比单独治疗更能增强骨强度,可以为骨质疏松症提供最佳保护。

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