Abstract

Daily cyclic changes in environmental conditions are key signals for anticipatory and adaptive adjustments of most living species, including mammals. Lower ambient temperature stimulates the thermogenic activity of brown adipose tissue (BAT) and skeletal muscle. Given that the molecular components of the endogenous biological clock interact with thermal and metabolic mechanisms directly involved in the defense of body temperature, the present study evaluated the differential homeostatic responses to a cold stimulus at distinct time-windows of the light/dark-cycle. Male Wistar rats were subjected to a single episode of 3 h cold ambient temperature (4°C) at one of 6 time-points starting at Zeitgeber Times 3, 7, 11, 15, 19, and 23. Metabolic rate, core body temperature, locomotor activity (LA), feeding, and drinking behaviors were recorded during control and cold conditions at each time-point. Immediately after the stimulus, rats were euthanized and both the soleus and BAT were collected for real-time PCR. During the light phase (i.e., inactive phase), cold exposure resulted in a slight hyperthermia (p < 0.001). Light phase cold exposure also increased metabolic rate and LA (p < 0.001). In addition, the prevalence of fat oxidative metabolism was attenuated during the inactive phase (p < 0.001). These metabolic changes were accompanied by time-of-day and tissue-specific changes in core clock gene expression, such as DBP (p < 0.0001) and REV-ERBα (p < 0.01) in the BAT and CLOCK (p < 0.05), PER2 (p < 0.05), CRY1 (p < 0.05), CRY2 (p < 0.01), and REV-ERBα (p < 0.05) in the soleus skeletal muscle. Moreover, genes involved in substrate oxidation and thermogenesis were affected in a time-of-day and tissue-specific manner by cold exposure. The time-of-day modulation of substrate mobilization and oxidation during cold exposure provides a clear example of the circadian modulation of physiological and metabolic responses. Interestingly, after cold exposure, time-of-day mostly affected circadian clock gene expression in the soleus muscle, despite comparable changes in LA over the light-dark-cycle. The current findings add further evidence for tissue-specific actions of the internal clock in different peripheral organs such as skeletal muscle and BAT.

Highlights

  • Cyclic changes in environmental conditions are key signals for the adaptive and anticipatory activity of most living species, including mammals

  • Synchronized activation of the autonomic innervation to brown adipose tissue (BAT) and white adipose tissue (WAT), liver, adrenal, and skeletal muscle is necessary to produce the necessary amount of energy and heat to keep body temperature within safe levels during cold exposure [7]

  • The main finding of the present study is that the cold-induced metabolic response and changes in gene expression in BAT and muscle differ depending on the time-of-day of the cold exposure

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Summary

Introduction

Cyclic changes in environmental conditions are key signals for the adaptive and anticipatory activity of most living species, including mammals. It is well known that a cold environment induces autonomic, cardiovascular, metabolic, and behavioral adjustments that depend on the synchronized activation of multiple independent pathways resulting in thermal adaptation/acclimation [6]. These adjustments include physiological changes such as vasoconstriction (heat retention or storage) and thermogenesis from both the activation of brown adipose tissue (BAT) (nonshivering) and skeletal muscle involuntary contraction (shivering) [6]. Synchronized activation of the autonomic innervation to BAT and white adipose tissue (WAT), liver, adrenal, and skeletal muscle is necessary to produce the necessary amount of energy and heat to keep body temperature within safe levels during cold exposure [7]. Given that the molecular components of the endogenous biological clock interact with thermal and metabolic mechanisms directly involved in the defense of body temperature, the present study evaluated the differential homeostatic responses to a cold stimulus at distinct time­windows of the light/dark­cycle

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