Verbascoside Inhibits/Repairs the Damage of LPS-Induced Inflammation by Regulating Apoptosis, Oxidative Stress, and Bone Remodeling

被引:7
作者
Akyer, Sahika Pinar [1 ]
Karagur, Ege Riza [2 ]
Ata, Melek Tunc [3 ]
Toprak, Emine Kilic [3 ]
Donmez, Aysegul Cort [4 ]
Donmez, Baris Ozgur [1 ]
机构
[1] Pamukkale Univ, Sch Med, Dept Anat, Kinikli, Str 11, TR-20160 Denizli, Turkiye
[2] Pamukkale Univ, Sch Med, Dept Med Genet, Str 11, TR-20160 Denizli, Turkiye
[3] Pamukkale Univ, Sch Med, Dept Physiol, Str 11, TR-20160 Denizli, Turkiye
[4] Pamukkale Univ, Sch Med, Dept Med Biochem, Str 11, TR-20160 Denizli, Turkiye
关键词
MLO-Y4; cell; bone metabolism; verbascoside; LPS; bone proteins; OSTEOCYTE; PROTEIN; PRODUCTS; DISEASE; CELLS; RISK;
D O I
10.3390/cimb45110550
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Osteocytes play an important role as regulators of both osteoclasts and osteoblasts, and some proteins that are secreted from them play a role in bone remodeling and modeling. LPS affects bone structure because it is an inflammatory factor, despite verbascoside's potential for bone preservation and healing. Osteocytes may also be involved in the control of the bone's response to immunological changes in inflammatory situations. MLO-Y4 cells were cultured in either supplemented -MEM alone with a low serum to inhibit cell growth or media with LPS (10 ng/mL) and/or verbascoside (50 g/mL) to show the LPS effect. In our research, LPS treatment increased RANKL levels while decreasing OPG and RUNX2 expression. Treatment with verbascoside reduced RANKL expression. In our work, verbascoside increased the expression of OPG and RUNX2. In MLO-Y4 cells exposed to verbascoside, SOD, CAT, and GSH activities as well as the expression levels of bone mineralization proteins like PHEX, RUNX2, and OPG were all elevated.
引用
收藏
页码:8755 / 8766
页数:12
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