Dietary fat intake promotes the development of hepatic steatosis independently from excess caloric consumption in a murine model

• Published in: Metabolism, clinical and experimental Vol. 59; no. 8; pp. 1092 - 1105
• Main Authors: de Meijer, Vincent E, Le, Hau D, Meisel, Jonathan A, Sharif, M. Reza Akhavan, Pan, Amy, Nosé, Vânia, Puder, Mark
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01-08-2010; Elsevier
• Subjects: Alanine Transaminase - blood; Animals; Biological and medical sciences; Dietary Fats - administration & dosage; Disease Models, Animal; Endocrinology & Metabolism; Energy Intake; Fatty Liver - etiology; Feeding. Feeding behavior; Fundamental and applied biological sciences. Psychology; Gastroenterology. Liver. Pancreas. Abdomen; Hyperphagia - etiology; Liver - metabolism; Liver. Biliary tract. Portal circulation. Exocrine pancreas; Magnetic Resonance Spectroscopy; Male; Medical sciences; Mice; Mice, Inbred C57BL; Organ Size; Other diseases. Semiology; Stearoyl-CoA Desaturase - genetics; Sterol Regulatory Element Binding Protein 1 - genetics; Vertebrates: anatomy and physiology, studies on body, several organs or systems; Weight Gain; Vertebrata; Mammalia; Fatty liver; Mouse; Food intake; Animal; Rodentia; Fat; Digestive diseases; Hepatic disease; Models; Endocrinology
• ISSN: 0026-0495; 1532-8600
• DOI: 10.1016/j.metabol.2009.11.006

Abstract Nonalcoholic fatty liver disease results from overconsumption and is a significant and increasing cause of liver failure. The type of diet that is conducive to the development of this disease has not been established, and evidence-based treatment options are currently lacking. We hypothesized that the onset of hepatic steatosis is linked to the consumption of a diet with a high fat content, rather than related to excess caloric intake. In addition, we also hypothesized that fully manifested hepatic steatosis could be reversed by reducing the fat percentage in the diet of obese mice. C57BL/6J male mice were fed either a purified rodent diet containing 10% fat or a diet with 60% of calories derived from fat. A pair-feeding design was used to distinguish the effects of dietary fat content and caloric intake on dietary-induced hepatic lipid accumulation and associated injury. Livers were analyzed by quantitative reverse transcriptase polymerase chain reaction for lipid metabolism-related gene expression. After 9 weeks, mice on the 60%-fat diet exhibited more weight gain, insulin resistance, and hepatic steatosis compared with mice on a 10%-fat diet with equal caloric intake. Furthermore, mice with established metabolic syndrome at 9 weeks showed reversal of hepatic steatosis, insulin resistance, and obesity when switched to a 10%-fat diet for an additional 9 weeks, independent of caloric intake. Quantitative reverse transcriptase polymerase chain reaction revealed that transcripts related to both de novo lipogenesis and increased uptake of free fatty acids were significantly up-regulated in mice pair-fed a 60%-fat diet compared with 10%-fat–fed animals. Dietary fat content, independent from caloric intake, is a crucial factor in the development of hepatic steatosis, obesity, and insulin resistance in the C57BL/6J diet-induced obesity model caused by increased uptake of free fatty acids and de novo lipogenesis. In addition, once established, all these features of the metabolic syndrome can be successfully reversed after switching obese mice to a diet low in fat. Low-fat diets deserve attention in the investigation of a potential treatment of patients with nonalcoholic fatty liver disease.