Cryptotanshinone, a lipophilic compound of Salvia miltiorrriza root, inhibits TNF-α-induced expression of adhesion molecules in HUVEC and attenuates rat myocardial ischemia/reperfusion injury in vivo

被引:84
作者
Jin, Yong Chun [1 ]
Kim, Chun Wook [1 ]
Kim, Young Min [1 ]
Nizamutdinova, Irina Tsoy [1 ]
Ha, Yu Mi [1 ]
Kim, Hye Jung [1 ]
Seo, Han Geuk [1 ]
Son, Kun Ho [2 ]
Jeon, Su Jin [2 ]
Kang, Sam Sik [3 ]
Kim, Yeong Shik [3 ]
Kam, Sung-Chul [4 ]
Lee, Jea Heun [1 ]
Chang, Ki Churl [1 ]
机构
[1] Gyeongsang Natl Univ, Sch Med, Dept Pharmacol, Jinju, South Korea
[2] Andong Natl Univ, Dept Food Sci & Nutr, Andong, South Korea
[3] Seoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul, South Korea
[4] Gyeongsang Natl Univ, Sch Med, Dept Urol, Jinju, South Korea
关键词
Cryptotanshinone; Myocardial ischemia and reperfusion injury; Microcirculation disturbance; NF-kB activation; Adhesion molecules; Inflammation; VASCULAR ENDOTHELIAL-CELLS; FACTOR-KAPPA-B; REPERFUSION; ISCHEMIA; NEUTROPHIL; ACTIVATION; PROTEIN-1; EXTRACT; HEART;
D O I
10.1016/j.ejphar.2009.04.038
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of the present study was to evaluate the protective effect of cryptotanshinone (CTS), one of active ingredients of Salvia miltiorrhiza root, on myocardial ischemia-reperfusion injury in rat due to inhibition of some inflammatory events that occur by NF-kB-activation during ischemia and reperfusion. Myocardial ischemia and reperfusion injury was induced by occluding the left anterior descending coronary artery for 30 min followed by either 2 h (biochemical analysis) or 24 h (myocardial function and infarct size measurement) reperfusion. CTS injected (i.v.) 10 min before ischemia and reperfusion insult. CTS significantly reduced the infarct size and improved ischemia and reperfusion-induced myocardial contractile dysfunction. Furthermore, CTS inhibited NF-kB translocation, expression of pro-inflammatory cytokines (TNF-alpha, IL-1 beta, IL-6), neutrophil infiltration and MPO activity in ischemic myocardial tissues. CTS also significantly reduced plasma levels of TNF-alpha, IL-1 beta due to ischemia and reperfusion. Interestingly, H2O2-stimulated NF-kB-luciferase activity and TNF-alpha-induced expression of vascular cell adhesion molecule-1 (VCAM-1) and intracellular adhesion molecule-1 (ICAM-1) expressions in human umbilical vein endothelial cells (HUVEC) were significantly inhibited by CTS. Taken together, it is concluded that CTS may attenuate ischemia and reperfusion-induced microcirculatory disturbances by inhibition of proinflammatory cytokine production, reduction of neutrophil infiltration and possibly inhibition of adhesion molecules through inhibition of NF-kB-activation during ischemia and reperfusion. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 97
页数:7
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