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Age-Related Loss in Bone Mineral Density of Rats Fed Lifelong on a Fish Oil-Based Diet Is Avoided by Coenzyme Q10 Addition

机译:通过添加辅酶Q10避免了以鱼油为基础的饮食终生饲喂的大鼠年龄相关的骨矿物质密度损失

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摘要

During aging, bone mass declines increasing osteoporosis and fracture risks. Oxidative stress has been related to this bone loss, making dietary compounds with antioxidant properties a promising weapon. Male Wistar rats were maintained for 6 or 24 months on diets with fish oil as unique fat source, supplemented or not with coenzyme Q10 (CoQ10), to evaluate the potential of adding this molecule to the n-3 polyunsaturated fatty acid (n-3 PUFA)-based diet for bone mineral density (BMD) preservation. BMD was evaluated in the femur. Serum osteocalcin, osteopontin, receptor activator of nuclear factor-κB ligand, ostroprotegerin, parathyroid hormone, urinary F2-isoprostanes, and lymphocytes DNA strand breaks were also measured. BMD was lower in aged rats fed a diet without CoQ10 respect than their younger counterparts, whereas older animals receiving CoQ10 showed the highest BMD. F2-isoprostanes and DNA strand breaks showed that oxidative stress was higher during aging. Supplementation with CoQ10 prevented oxidative damage to lipid and DNA, in young and old animals, respectively. Reduced oxidative stress associated to CoQ10 supplementation of this n-3 PUFA-rich diet might explain the higher BMD found in aged rats in this group of animals.
机译:在衰老期间,骨质下降,增加了骨质疏松症和骨折的风险。氧化应激与骨质流失有关,这使得具有抗氧化特性的膳食化合物成为有前途的武器。将雄性Wistar大鼠以鱼油为唯一脂肪来源,并辅以或不辅以辅酶Q10(CoQ10)的饮食维持6或24个月,以评估将该分子添加至n-3多不饱和脂肪酸(n-3以PUFA为基础的饮食,可保护骨骼矿物质密度(BMD)。在股骨中评估BMD。还测量了血清骨钙素,骨桥蛋白,核因子-κB配体的受体激活剂,骨轮蛋白,甲状旁腺激素,尿中的F2-异前列腺素和淋巴细胞的DNA链断裂。饲喂无CoQ10饮食的老年大鼠的BMD低于年轻大鼠,而接受CoQ10的老年动物的BMD最高。 F2-异前列腺素和DNA链断裂表明,老化过程中氧化应激较高。补充CoQ10分别防止了幼小和成年动物对脂质和DNA的氧化损伤。富含这种富含n-3 PUFA饮食的辅酶Q10引起的氧化应激降低可能解释了这组动物中老年大鼠中发现的较高BMD。

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