Frankincense and myrrh suppress inflammation via regulation of the metabolic profiling and the MAPK signaling pathway

被引:47
|
作者
Su, Shulan [1 ,2 ,3 ]
Duan, Jinao [1 ,2 ,3 ]
Chen, Ting [1 ,2 ,3 ]
Huang, Xiaochen [1 ,2 ,3 ]
Shang, Erxin [1 ,2 ,3 ]
Yu, Li [1 ,2 ,3 ]
Wei, Kaifeng [4 ]
Zhu, Yue [1 ,2 ,3 ]
Guo, Jianming [1 ,2 ,3 ]
Guo, Sheng [1 ,2 ,3 ]
Liu, Pei [1 ,2 ,3 ]
Qian, Dawei [1 ,2 ,3 ]
Tang, Yuping [1 ,2 ,3 ]
机构
[1] Natl & Local Collaborat Engn Ctr Chinese Med Reso, Jiangsu Collaborat Innovat Ctr Chinese Med Resour, Nanjing 210023, Jiangsu, Peoples R China
[2] Nanjing Univ Chinese Med, Nanjing 210023, Jiangsu, Peoples R China
[3] Nanjing Univ Chinese Med, Jiangsu Key Lab High Technol Res TCM Formulae, Nanjing 210023, Jiangsu, Peoples R China
[4] Nanjing Univ Chinese Med, Basic Med Coll, Nanjing 210023, Jiangsu, Peoples R China
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
基金
中国国家自然科学基金;
关键词
ADJUVANT-INDUCED ARTHRITIS; RHEUMATOID-ARTHRITIS; NITRIC-OXIDE; SJOGRENS-SYNDROME; BOSWELLIC ACIDS; RISK; GLUCOCORTICOIDS; PATHOGENESIS; EXTRACT;
D O I
10.1038/srep13668
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Frankincense and myrrh are highly effective in treatment of inflammatary diseases, but lacking of the therapy mechanisms. We undertook this stuty to evaluate the effects on Adjuvant-induced Arthritis (AIA) rats and to explore the underlying mechanisms by analyzing the metabolic profiling and signaling pathway evaluated by expression of inflammatory cytokines, c-jun and c-fos and corresponding phosphorylation levels. The results stated the elevated expression levels of TNFa, PGE(2), IL-2, NO, and MDA in serum and swelling paw of AIA rats were significantly decreased after treatment, which exerted more remarkable inhibitive effects of combined therapy. The metbolic profiling of plasma and urine were clearly improved and twenty-one potential biomarkers were identified. Moreover, the inhibited effects of five bioactive components on cytokine transcription in PHA stimulated-PBMC showed the MAPK pathway might account for this phenomenon with considerable reduction in phosphorylated forms of all the three MAPK (ERK1/2, p38 and JNK) and down regulation of c-jun and c-fos.
引用
收藏
页数:14
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