Ameliorative effects of the traditional Chinese medicine formula Qing-Mai-Yin on arteriosclerosis obliterans in a rabbit model

被引:11
作者
Zhang, Lei [1 ]
Yuan, Jia-Qin [1 ]
Song, Fu-Chen [1 ]
Zhu, Mei-Dong [1 ]
Li, Qi [2 ]
Liu, Sheng-Hua [2 ]
Zhao, Kai [3 ]
Zhao, Cheng [4 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Yueyang Hosp Integrated Tradit Chinese & Western, Dept Vasc Surg, Shanghai, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Yueyang Clin Med Coll, Shanghai, Peoples R China
[3] Ningxia Med Univ, Gen Hosp, Dept Tradit Chinese Med, 804 Shengli Rd, Yinchuan 750004, Ningxia, Peoples R China
[4] Shanghai Univ Tradit Chinese Med, Shanghai TCM Integrated Hosp, Dept Vasc Dis, 110 Ganhe Rd, Shanghai 200437, Peoples R China
关键词
Inflammatory reactions; NF-kappa B signal; HPLC-Q-TOF-MS/MS; mechanisms; RED WINE; ATHEROSCLEROSIS; RESVERATROL; PHYTOCHEMISTRY; PHARMACOLOGY; PREVENTION; BOTANY; DAMAGE;
D O I
10.1080/13880209.2020.1803368
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Context: Qing-Mai-Yin(QMY) is a clinically used herbal formula for treating arteriosclerosis obliterans (ASO). Objective: To evaluate the chemical constituents and effects of QMY on ASO rabbit model. Materials and methods: Forty-eight New Zealand rabbits were divided into six groups (n = 8): normal (normal rabbits treated with 0.5% CMC-Na), vehicle (ASO rabbits treated with 0.5% CMC-Na), positive (simvastatin, 1.53 mg/kg), and QMY treatment (300, 600, and 1200 mg/kg). ASO rabbit model was prepared by high fatty feeding, roundly shortening artery, and bovine serum albumin immune injury. QMY (300, 600 and 1200 mg/kg) was orally administered for 8 weeks. The effects and possible mechanisms of QMY on ASO rabbits were evaluated by pathological examination, biochemical assays, and immunohistochemical assays. The compositions of QMY were analysed using HPLC-Q-TOF-MS/MS analysis. Results: Compared to the vehicle rabbit, QMY treatment suppressed plaque formation and intima thickness in aorta, and decreased intima thickness, whereas increased lumen area of femoral artery. Additionally, QMY treatment decreased TC, TG and LDL, decreased CRP and ET, and increased NO and 6-K-PGF1 alpha in serum. Furthermore, the potential mechanisms studied revealed that QMY treatment could suppress expression of TNF-alpha, IL-6, ICAM-1 and NF-kappa B in endothelial tissues, and increase I kappa B. In addition, HPLC analysis showed QMY had abundant anthraquinones, stilbenes, and flavonoids. Conclusion: QMY has ameliorative effects on ASO rabbit, and the potential mechanisms are correlated to reducing inflammation and down-regulating NF-kappa B. Our study provides a scientific basis for the future application and investigation of QMY.
引用
收藏
页码:785 / 795
页数:11
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