2-Methoxycinnamaldehyde from Cinnamomum cassia reduces rat myocardial ischemia and reperfusion injury in vivo due to HO-1 induction

被引:88
作者
Hwa, Jeong Seok [3 ,4 ]
Jin, Yong Chun [7 ]
Lee, Young Soo [1 ,2 ]
Ko, Young Shin [1 ,2 ]
Kim, Young Min [1 ,2 ]
Shi, Lian Yu [8 ]
Kim, Hye Jung [1 ,2 ]
Lee, Jae Heun [1 ,2 ]
Tran Minh Ngoc [5 ]
Bae, Ki Hwan [5 ]
Kim, Yeong Shik [6 ]
Chang, Ki Churl [1 ,2 ]
机构
[1] Gyeongsang Natl Univ, Dept Pharmacol, Sch Med, Jinju 660290, South Korea
[2] Gyeongsang Natl Univ, Inst Hlth Sci, Sch Med, Jinju 660290, South Korea
[3] Gyeongsang Natl Univ, Dept Urol, Sch Med, Jinju 660290, South Korea
[4] Gyeongsang Natl Univ, Inst Hlth Sci, Sch Med, Jinju 660290, South Korea
[5] Chungnam Natl Univ, Coll Pharm, Taejon, South Korea
[6] Seoul Natl Univ, Inst Nat Prod Res, Coll Pharm, Seoul, South Korea
[7] Yanbian Second Peoples Hosp, Jilin, Peoples R China
[8] Yanji Anorectal Hosp, Dept Gynecol & Obstet, Jilin, Peoples R China
关键词
2-Methoxycinnamaldehyde; Inflammation; HMGB1; VCAM-1; Heme oxygenase-1; Ischemia; Reperfusion injury; ALPHA-INDUCED EXPRESSION; NECROSIS-FACTOR-ALPHA; KAPPA-B ACTIVATION; HEME OXYGENASE-1; ADHESION MOLECULES; FREE-RADICALS; CINNAMALDEHYDE; CELL; ISCHEMIA/REPERFUSION; CONSTITUENTS;
D O I
10.1016/j.jep.2011.12.001
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Cinnamomum cassia Blume has been used as a traditional Chinese herbal medicine for alleviation of fever, inflammation, chronic bronchitis, and to improve blood circulation. Aim of the study: We addressed whether 2-methoxycinnamaldehyde (2-MCA), one of active ingredients of Cinnamomum cassia, reduces vascular cell adhesion molecule-1 (VCAM-1) expression in tumor necrosis factor-alpha (TNF-alpha)-activated endothelial cells and protects ischemia/reperfusion (I/R)-injury due to heme oxygenase (HO)-1 induction. Materials and methods: Adult male rats were subjected to 30 min of ischemia by occlusion of the left anterior descending coronary artery followed by 24 h of reperfusion. Rats were randomized to receive vehicle or 2-MCA (i.v.) 10 min before reperfusion. Results: Administration of 2-MCA significantly improved I/R-induced myocardial dysfunction by increasing the values of the first derivative (+/- dp/dr) of left ventricular pressure and decreased infarct size. In addition, 2-MCA reduced the expression of high mobility group box 1 (HMGB1), an activator of the inflammatory cascade when released into the extracellular space, and VCAM-1 in I/R myocardium along with increase of HO-1 induction. The reduced injury was accompanied by significantly reduction of neutrophils infiltration and increased SOD activity in ischemic tissues and reduced serum level of cardiac troponin I (cTnl). Furthermore, 2-MCA significantly increased HO-1 induction by translocation of Nrf-2 from cytosol to nucleus in endothelial cells. Inhibition of VCAM-1 expression by 2-MCA was reversed both by SnPPIX, a HO-1 inhibitor and siHO-1 RNA trasfection in TNF-alpha-activated cells. In addition, 2-MCA significantly inhibited NF-kappa B luciferase activity in TNF-alpha-activated endothelial cells. As expected, 2-MCA significantly inhibited monocyte (U937) adhesion to endothelial cells. Conclusion: We concluded that 2-MCA protects of myocardial I/R-injury due to antioxidant and anti-inflammatory action possibly by HO-1 induction which can be explained why Cinnamomum cassia has been used in inflammatory disorders. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:605 / 615
页数:11
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