Anti-inflammatory Effects of Baicalin, Baicalein, and Wogonin In Vitro and In Vivo

被引:249
作者
Lee, Wonhwa [1 ,2 ]
Ku, Sae-Kwang [3 ]
Bae, Jong-Sup [1 ]
机构
[1] Kyungpook Natl Univ, Coll Pharm, CMRI, Pharmaceut Sci Res Inst, Taegu 702701, South Korea
[2] Kyungpook Natl Univ, Plus KNU Biomed Convergence Program BK21, Dept Biochem & Cell Biol, Sch Med, Taegu 702701, South Korea
[3] Daegu Haany Univ, Dept Anat & Histol, Coll Korean Med, Gyongsan 712715, South Korea
基金
新加坡国家研究基金会;
关键词
baicalin; baicalein; wogonin; lipopolysaccharide; endothelium; inflammation; barrier integrity; PROTEIN-C RECEPTOR; NF-KAPPA-B; NITRIC-OXIDE SYNTHASE; ENDOTHELIAL BARRIER DYSFUNCTION; CELL-ADHESION MOLECULES; GROUP BOX 1; TNF-ALPHA; INFLAMMATORY RESPONSES; DEPENDENT ACTIVATION; IMMUNE-RESPONSES;
D O I
10.1007/s10753-014-0013-0
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Here, three structurally related polyphenols found in the Chinese herb Huang Qui, namely baicalin, baicalein, and wogonin, were examined for its effects on inflammatory responses by monitoring the effects of baicalin, baicalein, and wogonin on lipopolysaccharide (LPS)-mediated vascular inflammatory responses. We found that each compound inhibited LPS-induced barrier disruption, expression of cell adhesion molecules (CAMs), and adhesion/transendothelial migration of monocytes to human endothelial cells. Each compound induced potent inhibition of phorbol-12-myristate 13-acetate and LPS-induced endothelial cell protein C receptor shedding. It also suppressed LPS-induced hyperpermeability and leukocytes migration in vivo. Furthermore, each compound suppressed the production of tumor necrosis factor-alpha or interleukin-6 and the activation of nuclear factor-kappa B or extracellular regulated kinases 1/2 by LPS. Moreover, treatment with each compound resulted in reduced LPS-induced lethal endotoxemia. These results suggest that baicalin, baicalein, and wogonin posses anti-inflammatory functions by inhibiting hyperpermeability, expression of CAMs, and adhesion and migration of leukocytes, thereby endorsing its usefulness as a therapy for vascular inflammatory diseases.
引用
收藏
页码:110 / 125
页数:16
相关论文
共 89 条
[1]
Endothelium as a therapeutic target in sepsis [J].
Aird, William C. .
CURRENT DRUG TARGETS, 2007, 8 (04) :501-507
[2]
Effects of phosphatidylserine on p38 mitogen activated protein kinase, cyclic AMP responding element binding protein and nuclear factor-κB activation in resting and activated microglial cells [J].
Ajmone-Cat, MA ;
De Simone, R ;
Nicolini, A ;
Minghetti, L .
JOURNAL OF NEUROCHEMISTRY, 2003, 84 (02) :413-416
[3]
Nitric oxide synthases: structure, function and inhibition [J].
Alderton, WK ;
Cooper, CE ;
Knowles, RG .
BIOCHEMICAL JOURNAL, 2001, 357 (03) :593-615
[4]
Polyphosphate elicits pro-inflammatory responses that are counteracted by activated protein C in both cellular and animal models [J].
Bae, J. -S. ;
Lee, W. ;
Rezaie, A. R. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2012, 10 (06) :1145-1151
[5]
Barrier protective effects of lycopene in human endothelial cells [J].
Bae, Jae Woan ;
Bae, Jong-Sup .
INFLAMMATION RESEARCH, 2011, 60 (08) :751-758
[6]
Thrombin inhibits HMGB1-mediated proinflammatory signaling responses when endothelial protein C receptor is occupied by its natural ligand [J].
Bae, Jong-Sup ;
Rezaie, Alireza R. .
BMB REPORTS, 2013, 46 (11) :544-549
[8]
Activated protein C inhibits high mobility group box 1 signaling in endothelial cells [J].
Bae, Jong-Sup ;
Rezaie, Alireza R. .
BLOOD, 2011, 118 (14) :3952-3959
[9]
TNF-α drives remodeling of blood vessels and lymphatics in sustained airway inflammation in mice [J].
Baluk, Peter ;
Yao, Li-Chin ;
Feng, Jennifer ;
Romano, Talia ;
Jung, Sonia S. ;
Schreiter, Jessica L. ;
Yan, Li ;
Shealy, David J. ;
McDonald, Donald M. .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (10) :2954-2964
[10]
ENDOTOXIN-INDUCED ARTERIAL ENDOTHELIAL BARRIER DYSFUNCTION ASSESSED BY AN IN-VITRO MODEL [J].
BERMAN, RS ;
FREW, JD ;
MARTIN, W .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 110 (04) :1282-1284