Wang Xiaowei, Chen Liaobin, Peng Wei
Department of Orthopedics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, P.R. China.
Department of Orthopedics, The Third People's Hospital of Hubei, Wuhan 430033, P.R. China.
Exp Ther Med. 2017 Nov;14(5):5032-5038. doi: 10.3892/etm.2017.5147. Epub 2017 Sep 20.
The aim of the present study was to determine the protective effects of resveratrol on a rat model of osteoporosis and examine the associated mechanisms of its action. Rats were randomized into the following groups: Control, osteoporosis, osteoporosis + low-dose resveratrol, osteoporosis + middle-dose resveratrol and osteoporosis + high-dose resveratrol groups. Resveratrol treatment was administered 7 days after surgery for 8 weeks. ELISA assay was used to analyze alkaline phosphatase (ALP) and osteocalcin (OC) protein levels. Western blotting was performed to assess the protein expression of sirtuin 1 (SIRT1), nuclear factor (NF)-κB and NF-κB inhibitor (IkB) α. In the present study, the results indicated that resveratrol markedly improved the bone mineral density value, femoral porosity and bone mechanical tests in osteoporosis rats. Administration of resveratrol significantly decreased the serum levels of ALP and OC in rats with osteoporosis. Finally, treatment with resveratrol significantly promoted the protein expression of SIRT1, suppressed NF-κB and activated the IkBα protein expression in rats with osteoporosis. In conclusion, treatment with resveratrol significantly improved the final body weight of the osteoporosis rats via the SIRT1-NF-κB signaling pathway. The present study suggested that resveratrol exerted a protective effect on osteoporosis through activation of the SIRT1-NF-κB signaling pathway in rats.
本研究的目的是确定白藜芦醇对大鼠骨质疏松模型的保护作用,并探讨其相关作用机制。将大鼠随机分为以下几组:对照组、骨质疏松组、骨质疏松 + 低剂量白藜芦醇组、骨质疏松 + 中剂量白藜芦醇组和骨质疏松 + 高剂量白藜芦醇组。术后7天开始给予白藜芦醇治疗,持续8周。采用酶联免疫吸附测定(ELISA)法分析碱性磷酸酶(ALP)和骨钙素(OC)蛋白水平。进行蛋白质免疫印迹法检测沉默信息调节因子1(SIRT1)、核因子(NF)-κB和NF-κB抑制因子(IkB)α的蛋白表达。在本研究中,结果表明白藜芦醇显著改善了骨质疏松大鼠的骨密度值、股骨孔隙率和骨力学测试结果。给予白藜芦醇显著降低了骨质疏松大鼠血清中ALP和OC的水平。最后,白藜芦醇治疗显著促进了骨质疏松大鼠中SIRT1的蛋白表达,抑制了NF-κB,并激活了IkBα蛋白表达。总之,白藜芦醇通过SIRT1-NF-κB信号通路显著改善了骨质疏松大鼠的最终体重。本研究表明,白藜芦醇通过激活大鼠体内的SIRT1-NF-κB信号通路对骨质疏松发挥保护作用。