Tajima, Soichiro The University of Tokushima|Kyushu University
池田, 康将 The University of Tokushima 徳島大学 教育研究者総覧 KAKEN研究者をさがす
榎本, 英明 The University of Tokushima 徳島大学 教育研究者総覧
Imao, Mizuki The University of Tokushima
堀ノ内, 裕也 The University of Tokushima
(井澤)石澤, 有紀 The University of Tokushima 徳島大学 教育研究者総覧 KAKEN研究者をさがす
木平, 孝高 The University of Tokushima KAKEN研究者をさがす
宮本, 理人 The University of Tokushima KAKEN研究者をさがす
石澤, 啓介 The University of Tokushima 徳島大学 教育研究者総覧 KAKEN研究者をさがす
土屋, 浩一郎 The University of Tokushima 徳島大学 教育研究者総覧 KAKEN研究者をさがす
玉置, 俊晃 The University of Tokushima 徳島大学 教育研究者総覧 KAKEN研究者をさがす
Purpose: Angiotensin II (ANG II) has been shown to affect iron metabolism through alteration of iron transporters, leading to increased cellular and tissue iron contents. Serum ferritin, a marker of body iron storage, is elevated in various cardiovascular diseases, including hypertension. However, the associated changes in iron absorption and the mechanism underlying increased iron content in a hypertensive state remain unclear.
Methods: C57BL6/J mice were treated with ANG II to generate a model of hypertension. Mice were divided into 3 groups: (1) control, (2) ANG II-treated, and (3) ANG II-treated and ANG II receptor blocker (ARB)-administered (ANG II-ARB) groups.
Results: Mice treated with ANG II showed increased serum ferritin levels compared to vehicle-treated control mice. In ANG II-treated mice, duodenal divalent metal transporter-1 (DMT1) and ferroportin (FPN) expression levels were increased and hepatic hepcidin mRNA expression and serum hepcidin concentration were reduced. The mRNA expression of bone morphogenetic protein 6 (BMP6) and CCAAT/enhancer binding protein alpha (C/EBPα), which are regulators of hepcidin, was also down-regulated in the livers of ANG II-treated mice. In terms of tissue iron content, macrophage iron content and renal iron content were increased by ANG II treatment, and these increases were associated with reduced expression of transferrin receptor 1 and FPN and increased expression of ferritin. These changes induced by ANG II treatment were ameliorated by administration of an ARB.
Conclusions: ANG II altered the expression of duodenal iron transporters and reduced hepcidin levels, contributing to the alteration of body iron distribution.
European Journal of Nutrition
Springer Berlin Heidelberg
The final publication is available at link.springer.com.
ejn_54_5_709.pdf 1.96 MB