Effects of excess dietary iron and fat on glucose and lipid metabolism

被引:69
作者
Choi, Joo Sun [1 ]
Koh, In-Uk [1 ]
Lee, Hyo Jung [1 ]
Kim, Won Ho [1 ]
Song, Jihyun [1 ]
机构
[1] Korea Natl Inst Hlth, Ctr Biomed Sci, Div Metab Dis, Chungbuk Do 363951, South Korea
关键词
High-fat diet; Iron overload; Insulin resistance; Hepcidin; Hepatic steatosis; SERUM FERRITIN CONCENTRATION; INSULIN-RESISTANCE; HEREDITARY HEMOCHROMATOSIS; REGULATORY PEPTIDE; OXIDATIVE STRESS; HEPATOMA-CELLS; ADIPOSE-TISSUE; HEPCIDIN; LIVER; OBESITY;
D O I
10.1016/j.jnutbio.2013.02.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose: Diets rich in fat and energy are associated with metabolic syndrome (MS). Increased body iron stores have been recognized as a feature of MS. High-fat diets (HFs), excess iron loading and MS are closely associated, but the mechanism linking them has not been clearly defined. We investigated the interaction between dietary fat and dietary Fe in the context of glucose and lipid metabolism in the body. Methods: C57BL6/J mice were divided into four groups and fed the modified AIN-93G low-fat diet (LF) and HF with adequate or excess Fe for 7 weeks. The Fe contents were increased by adding carbonyl iron (2% of diet weight) (LF+Fe and HF+Fe). Results: High iron levels increased blood glucose levels but decreased high-density lipoprotein cholesterol levels. The HF group showed increases in plasma levels of glucose and insulin and insulin resistance. HF+Fe mice showed greater changes. Representative indices of iron status, such hepatic and plasma Fe levels, were not altered further by the HF. However, both the HF and excess iron loading changed the hepatic expression of hepcidin and ferroportin. The LF+Fe, HF and HF+Fe groups showed greater hepatic fat accumulation compared with the LF group. These changes were paralleled by alterations in the levels of enzymes related to hepatic gluconeogenesis and lipid synthesis, which could be due to increases in mitochondrial dysfunction and oxidative stress. Conclusions: High-fat diets and iron overload are associated with insulin resistance, modified hepatic lipid and iron metabolism and increased mitochondrial dysfunction and oxidative stress. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:1634 / 1644
页数:11
相关论文
共 41 条
[1]   Pathways underlying iron accumulation in human nonalcoholic fatty liver disease [J].
Aigner, Elmar ;
Theurl, Igor ;
Theurl, Milan ;
Lederer, Dieter ;
Haufe, Heike ;
Dietze, Otto ;
Strasser, Michael ;
Datz, Christian ;
Weiss, Guenter .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2008, 87 (05) :1374-1383
[2]   Increased adipose tissue expression of hepcidin in severe obesity is independent from diabetes and NASH [J].
Bekri, Soumeya ;
Gual, Philippe ;
Anty, Rodolphe ;
Luciani, Nathalie ;
Dahman, Monsef ;
Ramesh, Bala ;
Iannelli, Antonio ;
Staccini-Myx, Aline ;
Casanova, Dominique ;
Ben Amor, Imed ;
Saint-Paul, Marie-Christine ;
Huet, Pierre-Michel ;
Sadoul, Jean-Louis ;
Gugenheim, Jean ;
Srai, Surjit Kaila S. ;
Tran, Albert ;
Le Marchand-Brustel, Yannick .
GASTROENTEROLOGY, 2006, 131 (03) :788-796
[3]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[4]   Troglitazone action is independent of adipose tissue [J].
Burant, CF ;
Sreenan, S ;
Hirano, KI ;
Tai, TAC ;
Lohmiller, J ;
Lukens, J ;
Davidson, NO ;
Ross, S ;
Graves, RA .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (11) :2900-2908
[5]   Leptin increases the expression of the iron regulatory hormone hepcidin in HuH7 human hepatoma cells [J].
Chung, Bomee ;
Matak, Pavle ;
McKie, Andrew T. ;
Sharp, Paul .
JOURNAL OF NUTRITION, 2007, 137 (11) :2366-2370
[6]   Dietary iron restriction or iron chelation protects from diabetes and loss of β-cell function in the obese (ob/ob lep-/-) mouse [J].
Cooksey, Robert C. ;
Jones, Deborah ;
Gabrielsen, Scott ;
Huang, Jingyu ;
Simcox, Judith A. ;
Luo, Bai ;
Soesanto, Yudi ;
Rienhoff, Hugh ;
Abel, E. Dale ;
McClain, Donald A. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2010, 298 (06) :E1236-E1243
[7]   Iron depletion by deferoxamine up-regulates glucose uptake and insulin signaling in hepatoma cells and in rat liver [J].
Dongiovanni, Paola ;
Valenti, Luca ;
Fracanzani, Anna Ludovica ;
Gatti, Stefano ;
Cairo, Gaetano ;
Fargion, Silvia .
AMERICAN JOURNAL OF PATHOLOGY, 2008, 172 (03) :738-747
[8]   Diabetes and serum ferritin concentration among US adults [J].
Ford, ES ;
Cogswell, ME .
DIABETES CARE, 1999, 22 (12) :1978-1983
[9]  
FRIEDEWALD WT, 1972, CLIN CHEM, V18, P499
[10]   Increased oxidative stress in obesity and its impact on metabolic syndrome [J].
Furukawa, S ;
Fujita, T ;
Shimabukuro, M ;
Iwaki, M ;
Yamada, Y ;
Nakajima, Y ;
Nakayama, O ;
Makishima, M ;
Matsuda, M ;
Shimomura, I .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (12) :1752-1761