A selective NFkB inhibitor, DHMEQ, reduced atherosclerosis in ApoE-deficient mice

被引:39
作者
Chiba, Tsuyoshi
Kondo, Yoshitaka
Shinozaki, Shohei
Kaneko, Eiji
Ishigami, Akihito
Maruyama, Naoki
Umezawa, Kazuo
Shimokado, Kentaro
机构
[1] Tokyo Med & Dent Univ, Grad Sch, Bunkyo Ku, Tokyo 1138619, Japan
[2] Tokyo Metropolitan Inst Gerontol, Tokyo, Japan
[3] Keio Univ, Fac Sci & Technol, Dept Appl Chem, Tokyo 108, Japan
关键词
inflammation; hyperlipidemia; TNF-alpha;
D O I
10.5551/jat.13.308
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Background and Purpose: Atherosclerosis is a chronic inflammatory process, and anti-inflammatory agents potentially inhibit the development of atherosclerosis. We tested whether a novel NFkB inhibitor reduces atherosclerosis. Methods: Dehydroxymethylepoxyquinomicin (10 mg/kg) or vehicle (chloromethyl cellulose) was injected intraperitoneally into apoE-deficient mice three times a week for 16 weeks. The entire aorta was excised and atherosclerotic area was determined at 4 and 16 weeks. Serum levels of cholesterol, triglyceride, TNF-alpha and adiponectin were also measured. Results: The atherosclerotic area was significantly smaller in mice treated with dehydroxymethyl-epoxyquinomicin both at 4 and 16 weeks. There was no significant difference in body weight or serum levels of cholesterol, triglyceride, and adiponectin. Conclusions: A new NFkB inhibitor, dehydroxymethylepoxyquinomicin, reduced atherosclerosis without affecting plasma lipid levels in apoE-deficient mice.
引用
收藏
页码:308 / 313
页数:6
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