Diabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.
Food and Pharmacy College, Xuchang University, 88 Bayi Road, Xuchang 461000, China.
Nutrients. 2024 May 10;16(10):1443. doi: 10.3390/nu16101443.
Recent interest in preventing the development of osteoporosis has focused on the regulation of redox homeostasis. However, the action of lycopene (LYC), a strong natural antioxidant compound, on osteoporotic bone loss remains largely unknown. Here, we show that oral administration of LYC to OVX rats for 12 weeks reduced body weight gain, improved lipid metabolism, and preserved bone quality. In addition, LYC treatment inhibited ROS overgeneration in serum and bone marrow in OVX rats, and in BMSCs upon HO stimulation, leading to inhibiting adipogenesis and promoting osteogenesis during bone remodeling. At the molecular level, LYC improved bone quality via an increase in the expressions of FoxO1 and Runx2 and a decrease in the expressions of PPARγ and C/EBPα in OVX rats and BMSCs. Collectively, these findings suggest that LYC attenuates osteoporotic bone loss through promoting osteogenesis and inhibiting adipogenesis via regulation of the FoxO1/PPARγ pathway driven by oxidative stress, presenting a novel strategy for osteoporosis management.
最近,人们对预防骨质疏松症的发展的兴趣集中在调节氧化还原平衡上。然而,番茄红素(LYC)作为一种强大的天然抗氧化化合物,其对骨质疏松性骨丢失的作用在很大程度上尚不清楚。在这里,我们表明,LYC 经口给予去卵巢大鼠 12 周可减少体重增加,改善脂代谢,并保持骨质量。此外,LYC 治疗抑制了 OVX 大鼠血清和骨髓中 ROS 的过度生成,以及 HO 刺激下 BMSCs 中的 ROS 过度生成,从而在骨重塑过程中抑制脂肪生成并促进成骨。在分子水平上,LYC 通过增加 OVX 大鼠和 BMSCs 中 FoxO1 和 Runx2 的表达,降低 PPARγ和 C/EBPα的表达,改善了骨质量。总之,这些发现表明,LYC 通过调节由氧化应激驱动的 FoxO1/PPARγ 通路,促进成骨和抑制脂肪生成,从而减轻骨质疏松性骨丢失,为骨质疏松症的管理提供了一种新策略。