DanHong Injection inhibits the development of primary abdominal aortic aneurysms in apoE knockout mice

被引:4
|
作者
Liu, Mengyang [1 ,2 ]
Chen, Yuanli [2 ]
Yang, Xiaoxiao [2 ]
Zhang, Ling [2 ]
Zhao, Tao [3 ]
Zhao, Buchang [3 ]
Jia, Lifu [3 ]
Zhu, Yan [4 ]
Gao, Xiumei [4 ]
Zhang, Boli [4 ]
Li, Xiaoju [2 ]
Xiang, Rong [1 ,5 ]
Han, Jihong [1 ,2 ,5 ]
Duan, Yajun [1 ,2 ]
机构
[1] Nankai Univ, State Key Lab Med Chem Biol, Tianjin 300071, Peoples R China
[2] Nankai Univ, Coll Life Sci, Tianjin 300071, Peoples R China
[3] Buchang Pharmaceut Co Ltd, Xian 712000, Peoples R China
[4] Tianjin Univ Tradit Chinese Med, Tianjin 300071, Peoples R China
[5] Nankai Univ, Collaborat Innovat Ctr Biotherapy, Tianjin 300071, Peoples R China
来源
CHINESE SCIENCE BULLETIN | 2014年 / 59卷 / 13期
基金
中国国家自然科学基金;
关键词
Abdominal aortic aneurysms; DanHong Injection (DHI); MMP-2; MMP-9; MCP-1; MATRIX METALLOPROTEINASES; MATRIX-METALLOPROTEINASE-9; PATHOGENESIS; DOXYCYCLINE; EXPRESSION; GAMMA; ATHEROSCLEROSIS; BIOMARKERS; LIGANDS; GROWTH;
D O I
10.1007/s11434-014-0175-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Clinical observations indicate that DanHong Injection (DHI) can increase blood flow and reduce various syndromes in patients with cardiovascular disease. However, it still needs to define the function of DHI and the involved mechanisms in details, such as the protective effect on the development of primary abdominal aortic aneurysms (AAAs). In this study, we determined whether DHI is able to inhibit AAA in apoE knockout (apoE(-/-)) mice. Thirty apoE(-/-) male mice on high-fat diet (0.5 % cholesterol, 21 % fat) were randomly divided into two groups and received i.p. injection of saline (100 mu L/day) and DHI (100 mu L/day), respectively, for 16 weeks. At the end of experiment, we determined the development of atherosclerosis in en face aorta and aneurysms, pathological morphology of arterial wall, and serum lipid levels. We also determined the expression of monocyte chemoattractant protein-1 (MCP-1), MMP-2, and MMP-9 mRNA in aortic wall using real-time RT-PCR. Our results indicated that high-fat diet induced the development of AAAs in apoE(-/-) mice, but the induction was totally blocked by DHI (P < 0.01). The result of staining of abdominal aortic cross sections showed that DHI maintained the collagen content in arterial wall, thereby preventing the animals from the development of AAA. Although DHI had little effect on serum total- and LDL-cholesterol levels, it reduced the expression of MCP-1, MMP-2, and MMP-9 mRNA in aortic wall (P < 0.01). Taken together, our study suggests that DHI can inhibit the high-fat diet-induced AAA formation. The inhibitory effects may be related to the maintenance of the collagen content and inhibition of expression of AAA-related genes. Our study may suggest a new application of DHI in clinics.
引用
收藏
页码:1366 / 1373
页数:8
相关论文
共 50 条
  • [1] Danhong Injection Inhibits the Development of Atherosclerosis in Both Apoe-/- and Ldlr-/- Mice
    Chen, Yuanli
    Liu, Mengyang
    Zhao, Tao
    Zhao, Buchang
    Jia, Lifu
    Zhu, Yan
    Zhang, Boli
    Gao, Xiumei
    Li, Guangliang
    Li, Xiaoju
    Xiang, Rong
    Han, Jihong
    Duan, Yajun
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2014, 63 (05) : 441 - 452
  • [2] Osteoprotegerin Prevents Development of Abdominal Aortic Aneurysms
    Bumdelger, Batmunkh
    Kokubo, Hiroki
    Kamata, Ryo
    Fujii, Masayuki
    Yoshimura, Koichi
    Aoki, Hiroki
    Orita, Yuichi
    Ishida, Takafumi
    Ohtaki, Megu
    Nagao, Masataka
    Ishida, Mari
    Yoshizumi, Masao
    PLOS ONE, 2016, 11 (01):
  • [3] Vasohibin-2 Aggravates Development of Ascending Aortic Aneurysms but not Abdominal Aortic Aneurysms nor Atherosclerosis in ApoE-Deficient Mice
    Otaka, Nozomu
    Uchida, Haruhito A.
    Okuyama, Michihiro
    Hada, Yoshiko
    Onishi, Yasuhiro
    Kakio, Yuki
    Takeuchi, Hidemi
    Umebayashi, Ryoko
    Tanabe, Katsuyuki
    Subramanian, Venkateswaran
    Daugherty, Alan
    Sato, Yasufumi
    Wada, Jun
    AMERICAN JOURNAL OF HYPERTENSION, 2021, 34 (05) : 467 - 475
  • [4] Ulinastatin Inhibits the Formation and Progression of Experimental Abdominal Aortic Aneurysms
    Li, Gang
    Zhou, Hua
    He, Yuxiang
    Sun, Shunji
    Wu, Xuejun
    Yuan, Hai
    JOURNAL OF VASCULAR RESEARCH, 2020, 57 (02) : 58 - 64
  • [5] Benzo[a]pyrene Potentiates the Pathogenesis of Abdominal Aortic Aneurysms in Apolipoprotein E Knockout Mice
    Prins, Petra A.
    Perati, Prudhvidhar R.
    Kon, Valentina
    Guo, Zhongmao
    Ramesh, Aramandla
    Linton, MacRae F.
    Fazio, Sergio
    Sampson, Uchechukwu K.
    CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2012, 29 (1-2) : 121 - 130
  • [6] Clarithromycin suppresses the periodontal bacteria-accelerated abdominal aortic aneurysms in mice
    Aoyama, N.
    Suzuki, J. -I.
    Ogawa, M.
    Watanabe, R.
    Kobayashi, N.
    Hanatani, T.
    Yoshida, A.
    Ashigaki, N.
    Izumi, Y.
    Isobe, M.
    JOURNAL OF PERIODONTAL RESEARCH, 2012, 47 (04) : 463 - 469
  • [7] Development of pharmacotherapies for abdominal aortic aneurysms
    Weaver, Lauren M.
    Loftin, Charles D.
    Zhan, Chang-Guo
    BIOMEDICINE & PHARMACOTHERAPY, 2022, 153
  • [8] Animal Models in the Research of Abdominal Aortic Aneurysms Development
    Patelis, N.
    Moris, D.
    Schizas, D.
    Damaskos, C.
    Perrea, D.
    Bakoyiannis, C.
    Liakakos, T.
    Georgopoulos, S.
    PHYSIOLOGICAL RESEARCH, 2017, 66 (06) : 899 - 915
  • [9] Pharmacologically Induced Thoracic and Abdominal Aortic Aneurysms in Mice
    Kanematsu, Yasuhisa
    Kanematsu, Miyuki
    Kurihara, Chie
    Tsou, Tsung-Ling
    Nuki, Yoshitsugu
    Liang, Elena I.
    Makino, Hiroshi
    Hashimoto, Tomoki
    HYPERTENSION, 2010, 55 (05) : 1267 - U309
  • [10] Elevation of Plasma High-Density Lipoproteins Inhibits Development of Experimental Abdominal Aortic Aneurysms
    Torsney, Evelyn
    Pirianov, Grisha
    Charolidi, Nicoletta
    Shoreim, Azza
    Gaze, David
    Petrova, Slaveia
    Laing, Ken
    Meisinger, Trevor
    Xiong, Wanfen
    Baxter, B. Timothy
    Cockerill, Gillian W.
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2012, 32 (11) : 2678 - +