Anti-Inflammatory Effects, SAR, and Action Mechanism of Monoterpenoids from Radix Paeoniae Alba on LPS-Stimulated RAW264.7 Cells

被引:38
作者
Bi, Xiaoxu [1 ]
Han, Li [1 ]
Qu, Tiange [2 ]
Mu, Yu [1 ]
Guan, Peipei [1 ]
Qu, Xiaodan [1 ]
Wang, Zhanyou [1 ]
Huang, Xueshi [1 ]
机构
[1] Northeastern Univ, Coll Life & Hlth Sci, Shenyang 110819, Peoples R China
[2] Beijing Univ Chinese Med, Dongzhimen Hosp, Clin Med Coll 1, Beijing 100700, Peoples R China
基金
中国国家自然科学基金;
关键词
Radix Paeoniae Alba; monoterpenoids; paeoniflorins; paeonidanins; albiflorin; anti-inflammation; SAR; action mechanism; RAW; 264.7; CELLS; NO PRODUCTION; PAEONIFLORIN; LACTIFLORA; PATHWAY; INFLAMMATION; SUPPRESSION; INHIBITION; ACTIVATION; COMPONENTS;
D O I
10.3390/molecules22050715
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
Nine monoterpenoids from Radix Paeoniae Alba, including paeoniflorin derivatives, paeoniflorin (PF), 4-O-methylpaeoniflorin (MPF), 4-O-methylbenzoylpaeoniflorin (MBPF); paeonidanin derivatives, paeonidanin (PD), paeonidanin A (PDA), albiflorin derivatives, albiflorin (AF), benzoylalbiflorin (BAF), galloylalbiflorin (GAF), and debenzoylalbiflorin (DAF), were obtained in our previous phytochemistry investigations. Their anti-inflammatory effects were determined in the present study. The expression and production of pro-inflammatory cytokines in lipopolysaccharides (LPS)-stimulated RAW 264.7 cells were measured using an Elisa assay and nitric oxide (NO) release was determined using the Griess method. The results demonstrated that the most of the monoterpenoids suppressed the LPS-induced production of NO, interleukin-6 (IL-6), and tumor necrosis factor alpha (TNF-alpha). The anti-inflammatory activities of these monoterpenoids were closely related to their structural characteristics. Paeoniflorins and paeonidanins presented stronger anti-inflammatory activities than those of albiflorin derivatives. Furthermore, the action mechanisms of MBPF, having a strong anti-inflammatory effect, were investigated using quantitative reverse transcription polymerase chain reaction (RT-PCR) and Western blot methods. The results indicated that MBPF could down-regulate the mRNA and protein expression level of inducible nitric oxide synthase (iNOS) in LPS-stimulated RAW 264.7 cells. The mitogen-activated protein kinase (MAPK), phosphatidylinositol 3-kinase (PI3K)/AKT and nuclear factor kappa B (NF-kappa B) signaling pathways are involved in mediating the role of MBPF in suppressing the expression and production of pro-inflammatory cytokines in RAW 264.7 cells.
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页数:9
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