Literature DB >> 21909126

Combination of fluvastatin and losartan relieves atherosclerosis and macrophage infiltration in atherosclerotic plaques in rabbits.

Ya-Pei Yang1, Qiu-Li Dong, Xu-Hong Zhang, Yue-Hui Zhang, Li Zhu, Shu-Ying Li, Zhong-Zhi Liu, Hui Xu, Nan Wang, Hong Jiang, Chun-Xi Liu, Xian-Xi Liu, Bo Dong.   

Abstract

AIM: To investigate whether the combination of fluvastatin and losartan synergistically relieve atherosclerosis and plaque inflammation induced by a high-cholesterol diet in rabbits.
METHODS: Atherosclerosis was induced with a high-cholesterol diet for 3 months in 36 New Zealand white rabbits. The animals were randomly divided into model group, fluvastatin (10 mg·kg(-1)·d(-1)) group, losartan (25 mg·kg(-1)·d(-1)) group, and fluvastatin plus losartan group. After the 16-week treatments, the blood samples the animals were collected, and the thoracic aortas were examined immunohistochemically. The mRNA and protein expression levels of monocyte chemotactic protein-1 (MCP-1) were measured using RT-PCR and Western blot.
RESULTS: Compared to the treatment with losartan or fluvastatin alone, the combined treatment did not produce higher efficacy in reduction of blood cholesterol level. However, the combination did synergistically decrease the intimal and media thickness of thoracic aortas with significantly reduced macrophage infiltration and MCP-1 expression in the plaques.
CONCLUSION: The combined treatment with losartan and fluvastatin significantly inhibited atherosclerotic progress and reduced inflammation associated with atherosclerotic plaques.

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Year:  2011        PMID: 21909126      PMCID: PMC4010086          DOI: 10.1038/aps.2011.95

Source DB:  PubMed          Journal:  Acta Pharmacol Sin        ISSN: 1671-4083            Impact factor:   6.150


  23 in total

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2.  Attenuation of tissue P-selectin and MCP-1 expression and intimal proliferation by AT(1) receptor blockade in hyperlipidemic rabbits.

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Review 3.  Molecular mechanisms involved in atherosclerosis.

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Journal:  Herz       Date:  2002-11       Impact factor: 1.443

4.  Additive beneficial effects of losartan combined with simvastatin in the treatment of hypercholesterolemic, hypertensive patients.

Authors:  Kwang Kon Koh; Michael J Quon; Seung Hwan Han; Wook-Jin Chung; Jeong Yeal Ahn; Yiel-Hea Seo; Moon Ho Kang; Tae Hoon Ahn; In Suck Choi; Eak Kyun Shin
Journal:  Circulation       Date:  2004-11-29       Impact factor: 29.690

5.  Upregulation of lectinlike oxidized low-density lipoprotein receptor-1 expression contributes to the vein graft atherosclerosis: modulation by losartan.

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6.  Effect of fluvastatin, lovastatin, nifedipine and verapamil on the systemic exposure of nateglinide in rabbits.

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7.  In vivo detection of macrophages in a rabbit atherosclerotic model by time-resolved laser-induced fluorescence spectroscopy.

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8.  Angiotensin receptor blockade decreases markers of vascular inflammation.

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Review 10.  Interactions between the renin-angiotensin system and dyslipidemia: relevance in the therapy of hypertension and coronary heart disease.

Authors:  Balkrishna M Singh; Jawahar L Mehta
Journal:  Arch Intern Med       Date:  2003-06-09
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  2 in total

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Journal:  FASEB J       Date:  2016-04-08       Impact factor: 5.191

2.  Bu-shen-he-mai-fang (HMF) Decoction Inhibits Atherosclerosis by Improving Antioxidant and Anti-Inflammatory Activities in ApoE-deficient Mice.

Authors:  Qingqing Hao; Xu Chen; Xiaoming Zhou; Xiaoyu Wang; Xinran Cao; Xingjuan Chen; Yuehua Jiang; Feng Lu; Ke You; Chuanhua Yang; Bo Dong
Journal:  Int J Biomed Sci       Date:  2014-12
  2 in total

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