Dietary iron overload enhances Western diet induced hepatic inflammation and alters lipid metabolism in rats sharing similarity with human DIOS

• Published in: Scientific reports 2022-12, Vol.12 (1), p.21414-21414, Article 21414
• Main Authors: Fujiwara, Sakura, Izawa, Takeshi, Mori, Mutsuki, Atarashi, Machi, Yamate, Jyoji, Kuwamura, Mitsuru
• Format: Article
• Language: English
• Subjects: 692/420/256/2515; 692/699/1503/1607/2750; 692/699/1503/1607/2751; 692/699/1702/393; 692/699/317; Animals; Body weight; Cholesterol; Cytokines; Diet; Diet, High-Fat - adverse effects; Diet, Western - adverse effects; Dyslipidemia; Fatty liver; High fat diet; Humanities and Social Sciences; Humans; Inflammation; Iron; Iron - metabolism; Iron Overload - metabolism; Iron, Dietary - metabolism; Kupffer cells; Lipid Metabolism; Liver - metabolism; Liver diseases; Lymphocytes T; Macrophages; Metabolic disorders; Metabolic syndrome; Metabolic Syndrome - metabolism; multidisciplinary; NF-κB protein; Non-alcoholic Fatty Liver Disease - metabolism; Nuclear transport; Rats; Science; Science (multidisciplinary); Steatosis; Translocation
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-022-25838-3

Hepatic iron overload is often concurrent with nonalcoholic fatty liver disease (NAFLD). Dysmetabolic iron overload syndrome (DIOS) is characterized by an increase in the liver and body iron stores and metabolic syndrome components. Increasing evidences suggest an overlap between NAFLD with iron overload and DIOS; however, the mechanism how iron is involved in their pathogenesis remains unclear. Here we investigated the role of iron in the pathology of a rat model of NAFLD with iron overload. Rats fed a Western (high-fat and high-fructose) diet for 26 weeks represented hepatic steatosis with an increased body weight and dyslipidemia. Addition of dietary iron overload to the Western diet feeding further increased serum triglyceride and cholesterol, and enhanced hepatic inflammation; the affected liver had intense iron deposition in the sinusoidal macrophages/Kupffer cells, associated with nuclear translocation of NFκB and upregulation of Th1/M1-related cytokines. The present model would be useful to investigate the mechanism underlying the development and progression of NAFLD as well as DIOS, and to elucidate an important role of iron as one of the "multiple hits” factors.