Rat brown adipose tissue thermogenic markers are modulated by estrous cycle phases and short‐term fasting

Author:

Dakic Tamara1ORCID,Velickovic Ksenija2ORCID,Lakic Iva1ORCID,Ruzicic Aleksandra1ORCID,Milicevic Andjela1,Plackic Nikola1,Vujovic Predrag1ORCID,Jevdjovic Tanja1ORCID

Affiliation:

1. Department for Comparative Physiology and Ecophysiology Institute for Physiology and Biochemistry, University of Belgrade‐Faculty for Biology Belgrade Serbia

2. Department of Cell and Tissue Biology Institute for Zoology, University of Belgrade‐Faculty of Biology Belgrade Serbia

Abstract

AbstractBrown adipose tissue (BAT) converts chemical energy into heat to maintain body temperature. Although fatty acids (FAs) represent a primary substrate for uncoupling protein 1 (UCP1)‐dependent thermogenesis, BAT also utilizes glucose for the same purpose. Considering that estrous cycle effects on BAT are not greatly explored, we examined those of 6‐h fasting on interscapular BAT (iBAT) thermogenic markers in proestrus and diestrus. We found that the percentage of multilocular adipocytes was lower in proestrus than in diestrus, although it was increased after fasting in both analyzed estrous cycle stages. Furthermore, the percentage of paucilocular adipocytes was increased by fasting, unlike the percentage of unilocular cells, which decreased in both analyzed stages of the estrous cycle. The UCP1 amount was lower in proestrus irrespectively of the examined dietary regimens. Regarding FA transporters, it was shown that iBAT CD36 content was increased in fasted rats in diestrus. In contrast to GLUT1, the level of GLUT4 was interactively modulated by selected estrous cycle phases and fasting. There was no change in insulin receptor and ERK1/2 activation, while AKT activation was interactively modulated by fasting and estrous cycle stages. Our study showed that iBAT exhibits morphological and functional changes in proestrus and diestrus. Moreover, iBAT undergoes additional dynamic functional and morphological changes during short‐term fasting to modulate nutrient utilization and adjust energy expenditure.

Publisher

Wiley

Subject

Clinical Biochemistry,Molecular Medicine,General Medicine,Biochemistry

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