Nakamura Ryosai, Kato Johji, Kitamura Kazuo, Onitsuka Hisamitsu, Imamura Takuroh, Cao Yuanning, Marutsuka Kousuke, Asada Yujiro, Kangawa Kenji, Eto Tanenao
First Department of Internal Medicine, Miyazaki Medical College, Kiyotake, Miyazaki 889-1692, Japan.
Circulation. 2004 Jul 27;110(4):426-31. doi: 10.1161/01.CIR.0000136085.34185.83. Epub 2004 Jul 19.
Adrenomedullin (AM) is expressed in cardiac tissue, and plasma AM levels increase in patients with acute myocardial infarction (MI). This study was performed to determine whether AM administration immediately after acute MI inhibits progression of heart failure in rats.
Rats were infused with 1.0 microg/h IP AM or saline over 7 days immediately after MI inducted by left coronary ligation and were examined 9 weeks after MI. Compared with the saline infusion, AM infusion significantly improved survival (59% versus 81%; P<0.05) and body weight gain (32%; P<0.01) and reduced heart weight (-28%; P<0.01), lung weight (-26%; P<0.01), left ventricular (LV) end-diastolic pressure (11.4+/-2.0 versus 4.0+/-0.6 mm Hg, mean+/- SEM; P<0.01), collagen volume fraction of noninfarcted LV (-39%; P<0.05), and plasma levels of endogenous rat AM (-38%; P<0.05) without affecting infarct size. To investigate the mechanism of AM actions, another series of MI rats infused with AM were killed on day 7. AM infusion had no effect on organ weights and hemodynamic parameters on day 7 of MI but significantly reduced urinary excretion of isoprostane (-61%; P<0.01) and noninfarcted LV mRNA levels of ACE (-31%; P<0.05) and p22-phox (-30%; P<0.05).
AM administration during the early period of MI improved the survival and ameliorated progression of LV remodeling and heart failure. This beneficial effect was accompanied by reductions in oxidative stress and ACE mRNA expression in noninfarcted LV in the AM infusion period.
肾上腺髓质素(AM)在心脏组织中表达,急性心肌梗死(MI)患者血浆AM水平升高。本研究旨在确定急性心肌梗死后立即给予AM是否能抑制大鼠心力衰竭的进展。
通过左冠状动脉结扎诱导心肌梗死后,大鼠立即接受7天腹腔内注射1.0μg/h的AM或生理盐水,并在心肌梗死后9周进行检查。与注射生理盐水相比,注射AM显著提高了生存率(59%对81%;P<0.05)和体重增加(32%;P<0.01),并减轻了心脏重量(-28%;P<0.01)、肺重量(-26%;P<0.01)、左心室(LV)舒张末期压力(11.4±2.0对4.0±0.6mmHg,平均值±标准误;P<0.01)、非梗死左心室的胶原体积分数(-39%;P<0.05)以及内源性大鼠AM的血浆水平(-38%;P<0.05),而不影响梗死面积。为了研究AM作用的机制,另一组注射AM的心肌梗死大鼠在第7天处死。在心肌梗死后第7天,注射AM对器官重量和血流动力学参数没有影响,但显著降低了异前列腺素的尿排泄量(-61%;P<0.01)以及非梗死左心室中ACE(-31%;P<0.05)和p22-吞噬氧化酶(-30%;P<0.05)的mRNA水平。
心肌梗死早期给予AM可提高生存率,改善左心室重构和心力衰竭的进展。这种有益作用伴随着AM注射期间非梗死左心室氧化应激和ACE mRNA表达的降低。