Cardioprotection of Asperosaponin X on experimental myocardial ischemia injury

被引:24
作者
Jiang, Wang-Lin [1 ,2 ]
Zhang, Shu-Ping [1 ]
Zhu, Hai-Bo [2 ]
Hou, Jian [2 ]
机构
[1] Binzhou Med Univ Yantai, Dept Pharm, Yantai 264003, Peoples R China
[2] Luye Pharma Grp Ltd, State Key Lab Long Acting & Targeting Drug Delive, Yantai 264003, Peoples R China
关键词
Asperosaponin X; Myocardial ischemia and reperfusion; High mobility group box-1 protein; Nuclear factor kappaB; Inflammatory response; FACTOR-KAPPA-B; MOBILITY GROUP BOX-1; CARDIAC TROPONIN-T; REPERFUSION INJURY; IN-VIVO; ENDOTHELIAL-CELLS; TNF-ALPHA; PROTEIN; INFARCTION; HMGB1;
D O I
10.1016/j.ijcard.2011.06.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Asperosaponin X was isolated from the roots of Dipsacus asper. In this study, we investigated the anti-myocardial ischemia and reperfusion (I/R) injury effects of Asperosaponin X in vivo and elucidated the potential mechanism in vitro. Results: Asperosaponin X significantly attenuated hypoxia-induced cytotoxicity in a concentration-dependent manner in H9c2 cells. Treatment of H9c2 cells with Asperosaponin X 5 mu M or 10 mu M blocked TNF-alpha-induced nuclear factor kappaB (NF-kappa B) phosphorylation by blocking HMGB1 expression. Treatment of rats with Asperosaponin X 10 mg/kg, (i.v.) protected the animals from myocardial I/R injury as indicated by a decrease in infarct volume, improvement in hemodynamics and reduction of myocardial damage severity. Treatment with Asperosaponin X also lowered serum levels of pro-inflammatory factors and reduced High mobility group box-1 protein (HMGB1), phosphorylated I kappa B-alpha and NF-kappa B expression in ischemic myocardial tissue. Additionally, continuous i.v. of Asperosaponin X 14 days attenuated cardiac remodeling. Conclusions: These protective effects suggested that Asperosaponin X may be due to block of myocardial inflammatory cascades through an HMGB1-dependent NF-kappa B signaling pathway. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:430 / 436
页数:7
相关论文
共 32 条
[21]  
Namba T, 1993, ENCY WAKAN YAKU TRAD, P185
[22]   High mobility group box 1 protein interacts with multiple Toll-like receptors [J].
Park, JS ;
Gamboni-Robertson, F ;
He, QB ;
Svetkauskaite, D ;
Kim, JY ;
Strassheim, D ;
Sohn, JW ;
Yamada, S ;
Maruyama, I ;
Banerjee, A ;
Ishizaka, A ;
Abraham, E .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2006, 290 (03) :C917-C924
[23]   Inhibitor of NK-κB Kinases α and β Are Both Essential for High Mobility Group Box 1-Mediated Chemotaxis [J].
Penzo, Marianna ;
Molten, Raffaella ;
Suda, Tomomi ;
Samaniego, Sylvia ;
Raucci, Angela ;
Habie, David M. ;
Miller, Frederick ;
Jiang, Hui-ping ;
Li, Jun ;
Pardi, Ruggero ;
Palumbo, Roberta ;
Olivotto, Eleonora ;
Kew, Richard R. ;
Bianchi, Marco E. ;
Marcu, Kenneth B. .
JOURNAL OF IMMUNOLOGY, 2010, 184 (08) :4497-4509
[24]   Ethics in the authorship and publishing of scientific articles [J].
Shewan, Louise G. ;
Coats, Andrew J. S. .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2010, 144 (01) :1-2
[25]   Nitric oxide synthase is the mediator of late preconditioning against myocardial infarction in conscious rabbits [J].
Takano, H ;
Manchikalapudi, S ;
Tang, XL ;
Qiu, YM ;
Rizvi, A ;
Jadoon, AK ;
Zhang, Q ;
Bolli, R .
CIRCULATION, 1998, 98 (05) :441-449
[26]   Innovative treatment programs against cancer -: II.: Nuclear factor-κB (NF-κB) as a molecular target [J].
Waddick, KG ;
Uckun, FM .
BIOCHEMICAL PHARMACOLOGY, 1999, 57 (01) :9-17
[27]   Chloride channel inhibition prevents ROS-dependent apoptosis induced by ischemia-reperfusion in mouse cardiomyocytes [J].
Wang, XM ;
Takahashi, N ;
Uramoto, H ;
Okada, Y .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2005, 16 (4-6) :147-154
[28]  
WU AHB, 1995, CLIN CHEM, V41, P1228
[29]   The cytokine activity of HMGB1 [J].
Yang, H ;
Wang, HC ;
Czura, CJ ;
Tracey, KJ .
JOURNAL OF LEUKOCYTE BIOLOGY, 2005, 78 (01) :1-8
[30]   Statins attenuate high mobility group box-1 protein induced vascular endothelial activation : a key role for TLR4/NF-κB signaling pathway [J].
Yang, Jun ;
Huang, Congxin ;
Yang, Jian ;
Jiang, Hong ;
Ding, Jiawang .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2010, 345 (1-2) :189-195