Department for Comparative Physiology and Ecophysiology, Institute for Physiology and Biochemistry, University of Belgrade-Faculty for Biology, Belgrade, Serbia.
Department of Cell and Tissue Biology, Institute for Zoology, University of Belgrade-Faculty of Biology, Belgrade, Serbia.
Biofactors. 2024 Jan-Feb;50(1):101-113. doi: 10.1002/biof.1993. Epub 2023 Jul 21.
Brown 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.
棕色脂肪组织 (BAT) 将化学能转化为热能以维持体温。虽然脂肪酸 (FAs) 是解偶联蛋白 1 (UCP1) 依赖性产热的主要底物,但 BAT 也利用葡萄糖达到同样的目的。考虑到发情周期对 BAT 的影响尚未得到充分探索,我们研究了发情前期和发情期 6 小时禁食对肩胛间 BAT (iBAT) 产热标志物的影响。我们发现,多房脂肪细胞的比例在发情前期低于发情期,但在两个发情周期阶段禁食后均增加。此外,与单房细胞的比例下降不同,多房脂肪细胞的比例因禁食而增加。UCP1 的含量在发情前期无论饮食方案如何均较低。关于 FA 转运体,发现在发情期禁食的大鼠中,iBAT 的 CD36 含量增加。与 GLUT1 不同,GLUT4 的水平受所选发情周期阶段和禁食的交互调节。胰岛素受体和 ERK1/2 的激活没有变化,而 AKT 的激活受禁食和发情周期阶段的交互调节。我们的研究表明,iBAT 在发情前期和发情期表现出形态和功能上的变化。此外,iBAT 在短期禁食期间还会发生额外的动态功能和形态变化,以调节营养物质的利用并调整能量消耗。