Pretreatment with Tongxinluo protects porcine myocardium from ischaemia/reperfusion injury through a nitric oxide related mechanism

被引:36
作者
Cheng Yu-tong
Yang Yue-jin [1 ]
Zhang Hai-tao
Qian Hai-yan
Zhao Jing-lin
Meng Xian-min [2 ]
Luo Fu-liang [3 ]
Wu Yi-ling
机构
[1] Fuwai Hosp, Peking Union Med Coll, Dept Cardiol, Ctr Coronary Heart Dis, Beijing 100037, Peoples R China
[2] Fuwai Hosp, Peking Union Med Coll, Core Lab, Beijing 100037, Peoples R China
[3] Fuwai Hosp, Peking Union Med Coll, Ctr Expt Anim, Beijing 100037, Peoples R China
关键词
myocardial infarction; myocardial reperfusion injury; nitric oxide; drugs; Chinese Herbal; neutrophil infiltration; NO-REFLOW PHENOMENON; K-ATP CHANNEL; CONTRAST ECHOCARDIOGRAPHY; ISCHEMIA-REPERFUSION; REACTIVE HYPEREMIA; SYNTHASE; INFARCTION; HEART; ISCHEMIA/REPERFUSION; INVOLVEMENT;
D O I
10.3760/cma.j.issn.0366-6999.2009.13.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The traditional Chinese medicine Tongxinluo can protect myocardium against ischaemia/reperfusion injury, but the mechanism of its action is not well documented. We examined the involvement of nitric oxide in the protective role of Tongxinluo. Methods Miniswine were randomized to four groups of seven: sham, control, Tongxinluo and Tongxinluo coadministration with a nitric oxide synthase inhibitor N-omega-nitro-L-arginine (L-NNA, 10 mg/kg i.v.). Three hours after administration of Tongxinluo, the animals were anaesthetised and the left anterior descending coronary artery ligated and maintained in situ for 90 minutes followed by 3 hours of reperfusion before death. Area of no reflow and necrosis and risk region were determined pathologically by planimetry. The degree of neutrophil accumulation in myocardium was obtained by measuring myeloperoxidase activity and histological analysis. Myocardial endothelial nitric oxide synthase activity and vascular endothelial cadherin content were measured by colorimetric method and immunoblotting analysis respectively. Results Tongxinluo significantly increased the local blood flow and limited the infarct and size of no reflow. Tongxinluo also attenuated myeloperoxidase activity and neutrophil accumulation in histological sections and maintained the level of vascular endothelial cadherin and endothelial nitric oxide synthase activity in the reflow region when compared with control group. The protection of Tongxinluo was counteracted by coadministration with L-NNA. Conclusions Tongxinluo may limit myocardial ischaemia and protect the heart against reperfusion injury. Tongxinluo regulates synthesis of nitric oxide by altering activity of endothelial nitric oxide synthase. Chin Med J 2009; 122(13):1529-1538
引用
收藏
页码:1529 / 1538
页数:10
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