Dyslipidemic high-fat diet affects adversely bone metabolism in mice associated with impaired antioxidant capacity

被引:72
作者
Xiao, Ying [1 ]
Cui, Jue [1 ]
Li, Ya-Xin [1 ]
Shi, Yong-Hui [1 ]
Wang, Bin [1 ]
Le, Guo-Wei [1 ]
Wang, Zhou-Ping [1 ]
机构
[1] Jiangnan Univ, Sch Food Sci & Technol, State Key Lab Food Sci & Technol, Wuxi, Peoples R China
关键词
Antioxidant; Oxidative stress; Hyperlipidemia; Bone formation; Bone resorption; IGF-1; TNF-a; KAPPA-B LIGAND; OXIDATIVE STRESS; RECEPTOR ACTIVATOR; GROWTH-HORMONE; MESSENGER-RNA; FREE-RADICALS; RESORPTION; ALPHA; DNA; ATHEROSCLEROSIS;
D O I
10.1016/j.nut.2009.11.012
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
Objective: The present study examined impacts of dyslipidemic high-fat diet on the bone antioxidant system and bone metabolism in growing mice. Furthermore, the relationship was studied between them. Methods: Male C57BL/6 mice (4 wk old) were fed with normal diet, high-fat diet (HFD), or HFD supplemented with 0.1% antioxidant lipoic acid (LA). After 13-wk feeding, the markers of plasma lipids status, bone metabolism in plasma and in urine, and femora oxidative stress were measured. To provide molecular evidence for abnormal bone metabolism affected by HFD, bone cell-specific mRNA levels were tested by real-time quantitative polymerase chain reaction. Moreover, insulin-like growth factor! and tumor necrosis factor-alpha in plasma and their mRNA levels in femur were measured. Results: The feeding dyslipidemic HFD induced both inhibitory bone formation reactions and enhancement of bone resorption reactions, accompanied by impaired bone antioxidant system, low levels of insulin-like growth factor I in plasma and in bone, and high levels of tumor necrosis factor-alpha in plasma but not in bone. In contrast, these alternatives were prevented completely or partially in mice fed LA supplement. Further, plasma propeptide of I collagen C-propeptide as a marker of bone formation was positively correlated with both total antioxidant capacity (r=0.683. P<0.001) and reduced glutathione/oxidized glutathione ratio (r = 0.565, P<0.003) of bone. Cross-linked N-telopeptides of bone type 1 collagen as a marker of bone resorption was negatively correlated with both total antioxidant capacity (r = -0.753, P<0.001) and glutathione/oxidized glutathione ratio (r=-0.786, P<0.001). Conclusion: Dyslipidemia induces impaired bone antioxidant system. Oxidative stress could be an important mediator of hyperlipidemia-induced bone loss. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:214 / 220
页数:7
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