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阿托伐他汀可减轻心脏移植小鼠模型中与移植相关的冠状动脉粥样硬化。

Atorvastatin attenuates transplant-associated coronary arteriosclerosis in a murine model of cardiac transplantation.

作者信息

Shirakawa Ibuki, Sata Masataka, Saiura Akio, Kaneda Yukari, Yashiro Hisako, Hirata Yasunobu, Makuuchi Masatoshi, Nagai Ryozo

机构信息

Department of Cardiovascular Medicine, University of Tokyo, Graduate School of Medicine, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.

出版信息

Biomed Pharmacother. 2007 Feb-Apr;61(2-3):154-9. doi: 10.1016/j.biopha.2006.09.017. Epub 2007 Jan 12.

Abstract

Accelerated coronary arteriosclerosis remains a major problem for the long-term survival of cardiac transplant recipients. However, the pathogenesis of transplant vasculopathy is poorly understood and there is no effective therapy. HMG-CoA reductase inhibitors, or statins, are widely prescribed to lower plasma cholesterol level. Accumulating evidence indicates that statins have various effects on vascular cells which are independent of their lipid-lowering effect. We investigated whether orally administered atorvastatin, one of the most potent statins, inhibits the development of intima hyperplasia in a mouse model of cardiac transplantation. Cardiac allografts from DBA mice were transplanted heterotopically into B10.D2 mice. Mice were administered either vehicle or atorvastatin everyday by gavage. Morphometrical analysis revealed that atorvastatin significantly reduced the development of coronary arteriosclerosis on the cardiac allografts harvested at one month. Immunohistochemical analysis revealed that atorvastatin attenuated infiltration of inflammatory cells with reduced expression of TGF-beta and adhesion molecules. These results suggest that atorvastatin may be effective in preventing transplant-associated arteriosclerosis along with other immunosuppressive agents.

摘要

加速性冠状动脉粥样硬化仍然是心脏移植受者长期存活的一个主要问题。然而,移植血管病的发病机制尚不清楚,且没有有效的治疗方法。HMG-CoA还原酶抑制剂,即他汀类药物,被广泛用于降低血浆胆固醇水平。越来越多的证据表明,他汀类药物对血管细胞有多种作用,这些作用与其降脂作用无关。我们研究了口服阿托伐他汀(最有效的他汀类药物之一)是否能抑制心脏移植小鼠模型中内膜增生的发展。将DBA小鼠的心脏同种异体移植物异位移植到B10.D2小鼠体内。每天通过灌胃给小鼠施用赋形剂或阿托伐他汀。形态计量学分析显示,阿托伐他汀显著减少了在一个月时收获的心脏同种异体移植物上冠状动脉粥样硬化的发展。免疫组织化学分析显示,阿托伐他汀减轻了炎症细胞的浸润,同时降低了TGF-β和黏附分子的表达。这些结果表明,阿托伐他汀可能与其他免疫抑制剂一起有效地预防移植相关的动脉硬化。

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