Xiao Jie, Shimada Miho, Liu Wenling, Hu Dayi, Matsumori Akira
Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Sakyo-ku, Kyoto 606-8507, Japan.
Eur J Heart Fail. 2009 Apr;11(4):349-53. doi: 10.1093/eurjhf/hfp023. Epub 2009 Feb 12.
Inflammation contributes to increased cardiovascular morbidity and mortality associated with activation of the renin-angiotensin-aldosterone system. The aim of this study was to investigate whether eplerenone, a selective aldosterone receptor antagonist, has anti-inflammatory effects on viral myocarditis.
Four-week-old inbred male DBA/2 mice were inoculated intraperitoneally with 10 plaque-forming units (pfu) of the encephalomyocarditis (EMC) virus. Mice were fed with standard chow (control) or with chow containing 2.5 mg/kg of eplerenone, starting either on day 0 (inoculation) or day 7. Survival at 28 days was significantly higher in the mice which started eplerenone treatment on day 0 (35 vs. 15% in controls, each n = 40, P < 0.05). The area of myocardial fibrosis on day 28 was significantly smaller in the eplerenone-treated mice than in controls (19.8 +/- 2.6%, n = 14, vs. 33.4 +/- 5.4%, n = 6, mean +/- SEM, P < 0.05). Gene expression of mouse mast cell proteases-4 and -5, matrix metalloproteinase-9, and type I procollagen on day 6 after EMC virus inoculation was significantly decreased in the hearts of eplerenone-treated mice.
These results suggest that eplerenone has anti-inflammatory effects, and exerts its beneficial effects on viral myocarditis by suppression of genes related to mast cells and cardiac remodelling in the hearts of mice.
炎症会导致与肾素 - 血管紧张素 - 醛固酮系统激活相关的心血管发病率和死亡率增加。本研究的目的是调查选择性醛固酮受体拮抗剂依普利酮对病毒性心肌炎是否具有抗炎作用。
给4周龄的近交系雄性DBA/2小鼠腹腔注射10个脑心肌炎(EMC)病毒空斑形成单位(pfu)。从第0天(接种日)或第7天开始,给小鼠喂食标准饲料(对照)或含2.5mg/kg依普利酮的饲料。在第0天开始依普利酮治疗的小鼠中,28天的存活率显著更高(对照组为15%,每组n = 40,依普利酮组为35%,P < 0.05)。依普利酮治疗的小鼠在第28天的心肌纤维化面积显著小于对照组(19.8 +/- 2.6%,n = 14,对照组为33.4 +/- 5.4%,n = 6,平均值 +/- 标准误,P < 0.05)。在EMC病毒接种后第6天,依普利酮治疗的小鼠心脏中鼠肥大细胞蛋白酶 -4和 -5、基质金属蛋白酶 -9以及I型前胶原的基因表达显著降低。
这些结果表明依普利酮具有抗炎作用,并通过抑制小鼠心脏中与肥大细胞和心脏重塑相关的基因,对病毒性心肌炎发挥有益作用。