Study of the protective mechanisms of Compound Danshen Tablet (Fufang Danshen Pian) against myocardial ischemia/reperfusion injury via the Akt-eNOS signaling pathway in rats

被引:86
作者
Qin Ren-an [1 ]
Lin Juan [2 ]
Li Chuyuan [1 ]
Fu Wenjuan [2 ]
Huang Chunyan [2 ]
Yu Xuemei [2 ]
Huang Lin [1 ]
Nie Hong [2 ]
机构
[1] Guangzhou Gen Med & Pharmaceut Res Inst, Guangzhou, Guangdong, Peoples R China
[2] Jinan Univ, Coll Pharm, Guangzhou 510632, Guangdong, Peoples R China
关键词
Compound Danshen Tablet; Myocardial ischemia/reperfusion injury; Akt; eNOS; Protective Mechanisms; Signaling pathway; ISCHEMIA-REPERFUSION INJURY; NITRIC-OXIDE; ALZHEIMERS-DISEASE; CELL-DEATH; CARDIOPROTECTION; INHIBITION; EXPRESSION; APOPTOSIS; MYOCYTES; PROTEIN;
D O I
10.1016/j.jep.2014.08.023
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Compound Danshen Tablet (CDT), an herbal preparation consisting of Salvia miltiorrhiza (Radix and rhizome of Salvia miltiorrhiza Bge.), Notoginseng (Radix and rhizome of Panax notoginseng (Burk.) F. H. Chen) and Borneolum Syntheticum, is widely used to improve coronary heart disease, cardiac angina and atherosclerosis in clinic in Asia and Pacific Ocean area, especially in China. Aim: The study is to research the protective mechanisms of Compound Danshen Tablet (CDT) against myocardial ischemia/reperfusion (MI/R) injury via the Akt-eNOS signaling Pathway in rats. Materials and methods: Rats were randomized into 7 groups: Sham group; Model group; Low-Dose CDT group (0.315 g/kg/d, i.g); Middle-Dose CDT group (0.63 g/kg/d, i.g); High-Dose CDT group (1.26 g/kg/d, i.g); Compound Danshen Dripping Pills (CDDP) group (0.0945 g/kg/d, i.g); Sulfotanshinone Sodium Injection (Tan II A) group (5 mg/kg/d, i.m). After the administration, the hearts of the rats were subjected to 30 min of coronary artery occlusion and 2 h of reperfusion except the Sham group rats. Results: CDT significantly decreased infarct size, apoptosis, caspase-3 protein expression, MDA level in myocardial tissues, the activities of serum CK, LDH and cTnI; on the contrary, it increased p-Akt, p-eNOS, bcl-2 protein expression, the activities of SOD and tissue LDH, and the level of NO. Conclusions: CDT can protect cardiomyocytes against MI/R injury and inhibits apoptosis in rats by activating Akt-eNOS signaling pathway. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:190 / 198
页数:9
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