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      Short-term food restriction followed by controlled refeeding promotes gorging behavior, enhances fat deposition, and diminishes insulin sensitivity in mice.

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          Abstract

          Rodents are commonly used in food restriction refeeding studies to investigate weight regain. Mice that are rationed food every 24 h may consume all allocated food in a short time (gorge) and therefore undergo a brief well-fed period followed by an extended fasted period until the next day's food allotment. These exaggerated metabolic states are not typical in mice fed ad libitum (nibbling). The aim of the current study was to elucidate the intraday and cumulative metabolic consequences of gorging (induced by food restriction) in mice during controlled refeeding. Accordingly, following a temporary food restriction, mice were fed rations similar to intakes of controls fed ad libitum. Temporary food restriction initiated gorging behavior that persisted during refeeding; consequently, metabolism-related measurements were obtained in the gorging mice during their daily fed and fasted metabolic states. Robust differences in adipose tissue lipogenic and inflammatory gene expression were found in the gorging mice by metabolic state (fed versus fasted). Additionally, despite a reduced cumulative food intake compared to mice fed ad libitum, restriction-induced gorging mice had increased intraabdominal fat accumulation, diminished hepatic and peripheral insulin sensitivity, and a gene expression profile favoring lipid deposition. Our findings highlight the intraday differences in gene expression in gorging mice before and after feeding that confound comparisons with mice fed ad libitum, or nibbling. The present study also provides evidence that weight regain following food restriction is associated with cumulative metabolic and behavioral abnormalities in mice.

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          Author and article information

          Journal
          J. Nutr. Biochem.
          The Journal of nutritional biochemistry
          Elsevier BV
          1873-4847
          0955-2863
          Jul 2015
          : 26
          : 7
          Affiliations
          [1 ] Department of Human Sciences, College of Education and Human Ecology, The Ohio State University, Columbus, OH 43210, USA.
          [2 ] Laboratory of Mitochondria and Metabolic Diseases/ Korea Mouse Metabolic Phenotyping Center, Lee Gil Ya Cancer and Diabetes Institute/ Molecular Medicine, Gachon University Graduate School of Medicine, Incheon 406-840, Korea.
          [3 ] Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06519, USA.
          [4 ] Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06519, USA; Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06519, USA; Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06519, USA.
          [5 ] Department of Human Sciences, College of Education and Human Ecology, The Ohio State University, Columbus, OH 43210, USA. Electronic address: Belury.1@osu.edu.
          Article
          S0955-2863(15)00055-8 NIHMS684176
          10.1016/j.jnutbio.2015.01.010
          4461460
          25913018
          3913f0ea-3c30-4795-bc0e-f4c0f4e5674c
          History

          Adiposity,Food restriction,Gorging,Insulin sensitivity,Refeeding,Weight regain

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