Anti-inflammatory effect of avenanthramides via NF-κB pathways in C2C12 skeletal muscle cells

被引:39
|
作者
Kang, Chounghun [2 ]
Shin, Woo Shik [3 ]
Yeo, Dongwook [1 ]
Lim, Wonchung [4 ]
Zhang, Tianou [1 ]
Ji, Li Li [1 ]
机构
[1] Univ Minnesota, Sch Kinesiol, Lab Physiol Hyg & Exercise Sci, Minneapolis, MN 55455 USA
[2] Inha Univ, Dept Phys Educ, Incheon, South Korea
[3] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[4] Cheongju Univ, Coll Hlth Sci, Dept Sports Med, Cheongju, South Korea
关键词
Avenanthramides; NF-kappa B; Inflammation; Skeletal muscle; TRANSCRIPTION FACTOR; ANTIOXIDANT ACTIVITY; OXIDATIVE STRESS; EXERCISE; OATS; POLYPHENOLS; MARKERS;
D O I
10.1016/j.freeradbiomed.2018.01.020
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
Avenanthramides (Avns), the polyphenol compounds found only in oats, have been shown to exhibit anti-inflammatory effects mainly by inhibiting nuclear factor (NF)-kappa B activation in select cell lines. However, the molecular mechanism by which Avns regulate the NF-kappa B pathway is still unclear. The purpose of this study was to investigate (1) the molecular mechanism by which three main fractions of Avns (AvnA, AvnB and AvnC) interact with I kappa B Kinase beta (IKK beta); and (2) whether this interaction results in reduced inflammatory responses in skeletal muscle cells. The protein-ligand docking and molecular dynamics simulation studies suggest that Avns acted as an allosteric inhibitor for modulating IKK beta's affinity for the NF-kappa B complex. Thus, Avns reduced IKK beta kinase activity in response to tert-butyl hydroperoxide (tBHP) stimulation and attenuated tBHP-induced TNF alpha and IL-1 beta mRNA expression. Furthermore, the three-fold increases in cyclooxygenase-2 (COX-2) protein and luciferase activity with tBHP treatment were reduced by 50% with Avns (P < .01), along with decreased prostaglandin E2 levels (P < .01). These data indicate that Avns are potent inhibitors of NF kappa B-mediated inflammatory response due to the downregulation of IKK beta activity in C2C12 cells.
引用
收藏
页码:30 / 36
页数:7
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