TY - JOUR
T1 - Association of dietary iron restriction with left ventricular remodeling after myocardial infarction in mice
AU - Eguchi, Akiyo
AU - Naito, Yoshiro
AU - Iwasaku, Toshihiro
AU - Okuhara, Yoshitaka
AU - Morisawa, Daisuke
AU - Sawada, Hisashi
AU - Nishimura, Koichi
AU - Oboshi, Makiko
AU - Fujii, Kenichi
AU - Mano, Toshiaki
AU - Masuyama, Tohru
AU - Hirotani, Shinichi
N1 - Publisher Copyright:
© 2015, Springer Japan.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - Several epidemiologic studies have reported that body iron status and dietary iron intake are related to an increased risk of acute myocardial infarction (MI). However, it is completely unknown whether dietary iron reduction impacts the development of left ventricular (LV) remodeling after MI. Here, we investigate the effect of dietary iron restriction on the development of LV remodeling after MI in an experimental model. MI was induced in C57BL/6 J mice (9–11 weeks of age) by the permanent ligation of the left anterior descending coronary artery (LAD). At 2 weeks after LAD ligation, mice were randomly divided into two groups and were given a normal diet or an iron-restricted diet for 4 weeks. Sham operation without LAD ligation was also performed as controls. MI mice exhibited increased LV dilatation and impaired LV systolic function that was associated with cardiomyocyte hypertrophy and interstitial fibrosis in the remote area, as compared with the controls at 6 weeks after MI. In contrast, dietary iron restriction attenuated LV dilatation and impaired LV systolic function coupled to cardiomyocyte hypertrophy and interstitial fibrosis in the remote area. Importantly, cardiac expression of cellular iron transport proteins, transferrin receptor 1 and divalent metal transporter 1 was increased in the remote area of MI mice compared with the controls. Dietary iron restriction attenuated the development of LV remodeling after MI in mice. Cellular iron transport might play a role in the pathophysiological mechanism of LV remodeling after MI.
AB - Several epidemiologic studies have reported that body iron status and dietary iron intake are related to an increased risk of acute myocardial infarction (MI). However, it is completely unknown whether dietary iron reduction impacts the development of left ventricular (LV) remodeling after MI. Here, we investigate the effect of dietary iron restriction on the development of LV remodeling after MI in an experimental model. MI was induced in C57BL/6 J mice (9–11 weeks of age) by the permanent ligation of the left anterior descending coronary artery (LAD). At 2 weeks after LAD ligation, mice were randomly divided into two groups and were given a normal diet or an iron-restricted diet for 4 weeks. Sham operation without LAD ligation was also performed as controls. MI mice exhibited increased LV dilatation and impaired LV systolic function that was associated with cardiomyocyte hypertrophy and interstitial fibrosis in the remote area, as compared with the controls at 6 weeks after MI. In contrast, dietary iron restriction attenuated LV dilatation and impaired LV systolic function coupled to cardiomyocyte hypertrophy and interstitial fibrosis in the remote area. Importantly, cardiac expression of cellular iron transport proteins, transferrin receptor 1 and divalent metal transporter 1 was increased in the remote area of MI mice compared with the controls. Dietary iron restriction attenuated the development of LV remodeling after MI in mice. Cellular iron transport might play a role in the pathophysiological mechanism of LV remodeling after MI.
KW - Iron
KW - Left ventricular remodeling
KW - Myocardial infarction
KW - Transferrin receptor 1
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U2 - 10.1007/s00380-014-0621-5
DO - 10.1007/s00380-014-0621-5
M3 - Article
C2 - 25573257
AN - SCOPUS:84957435581
SN - 0910-8327
VL - 31
SP - 222
EP - 229
JO - Heart and Vessels
JF - Heart and Vessels
IS - 2
ER -