A single day of high-fat diet feeding induces lipid accumulation and insulin resistance in brown adipose tissue in mice

Author:

Kuipers Eline N.12ORCID,Held Ntsiki M.3,in het Panhuis Wietse12,Modder Melanie12,Ruppert Philip M. M.4,Kersten Sander4,Kooijman Sander12,Guigas Bruno56,Houtkooper Riekelt H.3,Rensen Patrick C. N.12,Boon Mariëtte R.12

Affiliation:

1. Department of Medicine, Division of Endocrinology, Leiden University Medical Center, Leiden, The Netherlands

2. Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, The Netherlands

3. Laboratory Genetic Metabolic Diseases, Amsterdam University Medical Center, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands

4. Nutrition, Metabolism, and Genomics Group, Division of Human Nutrition and Health, Wageningen University, Wageningen, The Netherlands

5. Department of Parasitology, Leiden University Medical Center, Leiden, The Netherlands

6. Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, The Netherlands

Abstract

Brown adipose tissue (BAT) catabolizes glucose and fatty acids to produce heat and thereby contributes to energy expenditure. Long-term high-fat diet (HFD) feeding results in so-called ‘whitening’ of BAT characterized by increased lipid deposition, mitochondrial dysfunction, and reduced fat oxidation. The aim of the current study was to unravel the rate and related mechanisms by which HFD induces BAT whitening and insulin resistance. Wild-type mice were fed a HFD for 0, 1, 3, or 7 days. Within 1 day of HFD, BAT weight and lipid content were increased. HFD also immediately reduced insulin-stimulated glucose uptake by BAT, indicating rapid induction of insulin resistance. This was accompanied by a tendency toward a reduced uptake of triglyceride-derived fatty acids by BAT. Mitochondrial mass and Ucp1 expression were unaltered, whereas after 3 days of HFD, markers of mitochondrial dynamics suggested induction of a more fused mitochondrial network. Additionally, HFD also increased macrophage markers in BAT after 3 days of HFD. Counterintuitively, the switch to HFD was accompanied by an acute rise in core body temperature. We showed that a single day of HFD feeding is sufficient to induce the first signs of whitening and insulin resistance in BAT, which reduces the uptake of glucose and triglyceride-derived fatty acids. BAT whitening and insulin resistance are likely sustained by reduced mitochondrial oxidation due to changes in mitochondrial dynamics and macrophage infiltration, respectively. Likely, the switch to HFD swiftly induces thermogenesis in other metabolic organs, which allows attenuation of BAT thermogenesis.

Funder

Rembrandt Institute of Cardiovascular Science

Netherlands Heart Foundation

Dutch Diabetes Foundation

Netherlands Cardiovascular Research Initiative

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology,Endocrinology, Diabetes and Metabolism

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