Antioxidant Effect of Fructus Ligustri Lucidi Aqueous Extract in Ovariectomized Rats Is Mediated through Nox4-ROS-NF-κB Pathway

Purpose: This study is designed to explore whether Fructus ligustri lucidi (FLL) exhibits antioxidant effect in ovariectomized (OVX) rats, and to identify the signaling pathway involved in this process.Methods: OVX rats were treated with FLL aqueous extract (3.5 g/kg) for 12 weeks. Serum, uteri, and...

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Main Authors: Lili Wang (Author), Rufeng Ma (Author), Yubo Guo (Author), Jing Sun (Author), Haixia Liu (Author), Ruyuan Zhu (Author), Chenyue Liu (Author), Jun Li (Author), Lin Li (Author), Beibei Chen (Author), Liping Sun (Author), Jinfa Tang (Author), Dandan Zhao (Author), Fangfang Mo (Author), Jianzhao Niu (Author), Guangjian Jiang (Author), Min Fu (Author), Dieter Brömme (Author), Dongwei Zhang (Author), Sihua Gao (Author)
Format: Book
Published: Frontiers Media S.A., 2017-05-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Lili Wang  |e author 
700 1 0 |a Rufeng Ma  |e author 
700 1 0 |a Yubo Guo  |e author 
700 1 0 |a Jing Sun  |e author 
700 1 0 |a Haixia Liu  |e author 
700 1 0 |a Ruyuan Zhu  |e author 
700 1 0 |a Chenyue Liu  |e author 
700 1 0 |a Jun Li  |e author 
700 1 0 |a Lin Li  |e author 
700 1 0 |a Beibei Chen  |e author 
700 1 0 |a Liping Sun  |e author 
700 1 0 |a Jinfa Tang  |e author 
700 1 0 |a Dandan Zhao  |e author 
700 1 0 |a Fangfang Mo  |e author 
700 1 0 |a Jianzhao Niu  |e author 
700 1 0 |a Guangjian Jiang  |e author 
700 1 0 |a Min Fu  |e author 
700 1 0 |a Dieter Brömme  |e author 
700 1 0 |a Dongwei Zhang  |e author 
700 1 0 |a Sihua Gao  |e author 
245 0 0 |a Antioxidant Effect of Fructus Ligustri Lucidi Aqueous Extract in Ovariectomized Rats Is Mediated through Nox4-ROS-NF-κB Pathway 
260 |b Frontiers Media S.A.,   |c 2017-05-01T00:00:00Z. 
500 |a 1663-9812 
500 |a 10.3389/fphar.2017.00266 
520 |a Purpose: This study is designed to explore whether Fructus ligustri lucidi (FLL) exhibits antioxidant effect in ovariectomized (OVX) rats, and to identify the signaling pathway involved in this process.Methods: OVX rats were treated with FLL aqueous extract (3.5 g/kg) for 12 weeks. Serum, uteri, and tibias were harvested from the rats and the levels of total antioxidant capacity (TAC), nitric oxide (NO), malondialdehyde (MDA), 8-hydroxy-desoxyguanosine (8-OHdG), and superoxide dismutase (SOD) were determined. Changes in the levels of NF-κB-p65, phosphorylation of NF-κB-p65 (NF-κB-pp65), NF-κB inhibitor alpha (IκBα), phosphorylation of IκBα (p-IκBα), and NADPH oxidase 4 (Nox4) in uteri and tibias were determined by western blot, immunofluorescent and immunohistochemical analysis, respectively. In addition, the expression of cytochrome C (Cyto-C) and B-cell lymphoma-2 (Bcl-2) were determined in the tibias of rats. Histopathological changes in the bones were evaluated by hematoxylin-eosin staining. Bone mineral density (BMD) was determined in rat femurs by dual X-ray absorptiometry.Results: Treatment of OVX rats with FLL aqueous extract improved redox homeostasis by increasing the levels of TAC and NO as well as decreasing the levels of MDA and 8-OHdG in serum, tibias, and uteri. Further, FLL extract also downregulated the expression of Nox4, NF-κB-p65, NF-κB-pp65, and p-IκBα in the uteri and tibias. Furthermore, administration of FLL-OVX rats increased Bcl-2 expression and prevented cytoplasmic release of mitochondrial Cyto-C in the tibias. In addition, FLL treatment also improved bone microstructure and increased cortical bone thickness as well as increased BMD values in the femurs of OVX rats.Conclusions: FLL treatment may suppress oxidative stress response in OVX rats via regulating the Nox4/ROS/NF-κB signaling pathway. These results suggest the potential of using FLL as a natural antioxidant agent in preventing the development of osteoporosis. 
546 |a EN 
690 |a Fructus Ligustri Lucidi 
690 |a ovariectomy 
690 |a NADPH oxidase 4 (Nox4) 
690 |a nuclear factor kappa B (NF-κB) 
690 |a oxidative stress 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pharmacology, Vol 8 (2017) 
787 0 |n http://journal.frontiersin.org/article/10.3389/fphar.2017.00266/full 
787 0 |n https://doaj.org/toc/1663-9812 
856 4 1 |u https://doaj.org/article/4e63eaeae1d84d3ba0a949d0aa9fccb6  |z Connect to this object online.