Time of day determines postexercise metabolism in mouse adipose tissue

Author:

Pendergrast Logan A.1,Lundell Leonidas S.2,Ehrlich Amy M.2ORCID,Ashcroft Stephen P.2,Schönke Milena3,Basse Astrid L.2ORCID,Krook Anna3ORCID,Treebak Jonas T.2ORCID,Dollet Lucile23,Zierath Juleen R.123ORCID

Affiliation:

1. Department of Molecular Medicine and Surgery, Section for Integrative Physiology, Karolinska Institutet, SE-171 77 Stockholm, Sweden

2. Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark

3. Department of Physiology and Pharmacology, Section for Integrative Physiology, Karolinska Institutet, SE-171 77 Stockholm, Sweden

Abstract

The circadian clock is a cell-autonomous transcription–translation feedback mechanism that anticipates and adapts physiology and behavior to different phases of the day. A variety of factors including hormones, temperature, food-intake, and exercise can act on tissue-specific peripheral clocks to alter the expression of genes that influence metabolism, all in a time-of-day dependent manner. The aim of this study was to elucidate the effects of exercise timing on adipose tissue metabolism. We performed RNA sequencing on inguinal adipose tissue of mice immediately following maximal exercise or sham treatment at the early rest or early active phase. Only during the early active phase did exercise elicit an immediate increase in serum nonesterified fatty acids. Furthermore, early active phase exercise increased expression of markers of thermogenesis and mitochondrial proliferation in inguinal adipose tissue. In vitro, synchronized 3T3-L1 adipocytes showed a timing-dependent difference in Adrb2 expression, as well as a greater lipolytic activity. Thus, the response of adipose tissue to exercise is time-of-day sensitive and may be partly driven by the circadian clock. To determine the influence of feeding state on the time-of-day response to exercise, we replicated the experiment in 10-h-fasted early rest phase mice to mimic the early active phase metabolic status. A 10-h fast led to a similar lipolytic response as observed after active phase exercise but did not replicate the transcriptomic response, suggesting that the observed changes in gene expression are not driven by feeding status. In conclusion, acute exercise elicits timing-specific effects on adipose tissue to maintain metabolic homeostasis.

Funder

Novo Nordisk Fonden

Vetenskapsrådet

Svenska Diabetesstiftelsen

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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