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Abstract

Objective: Snacking, i.e., the intake of small amounts of palatable food items, is a common behavior in modern societies, promoting overeating and obesity. Shifting food intake into the daily rest phase disrupts circadian rhythms and is also known to stimulate weight gain. We therefore hypothesized that chronic snacking in the inactive phase may promote body weight gain and that this effect is based on disruption of circadian clocks. Methods: Male mice were fed a daily chocolate snack either during their rest or their active phase and body weight development and metabolic parameters were investigated. Snacking experiments were repeated in constant darkness and in clock-deficient mutant mice to examine the role of external and internal time cues in mediating the metabolic effects of snacking. Results: Chronic snacking in the rest phase increased body weight gain and disrupted metabolic circadian rhythms in energy expenditure, body temperature, and locomotor activity. Additionally, these rest phase snacking mice assimilated more energy during the inactive phase. Body weight remained increased in rest phase snacking wildtype mice in constant darkness as well as in clock-deficient mutant mice under a regular light–dark cycle compared to mice snacking in the active phase. Weight gain effects were abolished in clock-deficient mice in constant darkness. Conclusions: Our data suggest that mistimed snacking increases energy resorption and promotes body weight gain. This effect requires a functional circadian clock at least under constant darkness conditions.

Original languageEnglish
Article number101691
JournalMolecular Metabolism
Volume69
Pages (from-to)101691
ISSN2212-8778
DOIs
Publication statusPublished - 03.2023

Funding

We would like to thank Nadine Oster and Dr. Mariana Astiz for technical support. The infrared camera was kindly provided by Prof. Dr. Jens Mittag. This publication was supported by grants of the German Research Foundation: RTG-1957 ‘Adipocyte-Brain Crosstalk’, DFG (OE 723/2-1) to RO, and TR/CRC-296 ‘LocoTact’ (P13). TDM received funding from the German Research Foundation (DFG: TR/CRC-296 ‘LocoTact’ (P5), TRR152, SFB1123 and GRK 2816/1), the German Center for Diabetes Research (DZD) and the European Research Council ERC-CoG Trusted no.101044445.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being
  2. SDG 8 - Decent Work and Economic Growth
    SDG 8 Decent Work and Economic Growth
  3. SDG 10 - Reduced Inequalities
    SDG 10 Reduced Inequalities

Research Areas and Centers

  • Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)

DFG Research Classification Scheme

  • 2.22-17 Endocrinology, Diabetology, Metabolism

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