Department of Exercise Physiology, Faculty of Physical Education and Sports Science, Kharazmi University, Tehran, Iran.
Physiology of Exercise & Sport Lab, Department of Kinesiology, California State University, Long Beach, USA.
Mol Biol Rep. 2024 Aug 2;51(1):884. doi: 10.1007/s11033-024-09586-3.
Brown adipose tissue (BAT) is a thermogenic tissue that uncouples oxidative phosphorylation from ATP synthesis and increases energy expenditure via non-shivering thermogenesis in mammals. Cold exposure and exercise have been shown to increase BAT and browning of white adipose tissue (WAT) in mice. This study aimed to determine whether there is an additive effect of exercise during cold exposure on markers related to browning of adipose tissue. in Wistar rats.
Twenty-four male Wistar rats were randomly divided into three groups: Control (C, 25˚C), Swimming in Neutral (SN, 30˚C) water, and Swimming in Cold (SC, 15˚C) water. Swimming included intervals of 2-3 min, 1 min rest, until exhausted, three days a week for six weeks, with a training load of 3-6% body weight. After the experimental protocol, interscapular BAT and inguinal subcutaneous white adipose tissue (WAT) were excised, weighed, and processed for beiging marker gene expression.
SN and SC resulted in lower body weight gain, associated with reduced WAT and BAT volume and increased BAT number with greater effects observed in SC. Myostatin protein expression was lower in BAT, WAT, soleus muscle, and serum NC and SC compared to the C group. Expression of the interferon regulatory factor-4 (IRF4) gene in both BAT and WAT tissues was significantly greater in the SC than in the C. Expression of the PGC-1α in BAT was significantly increased in the SC compared to C and increased in WAT in NC and SC. Expression of the UCP1 in BAT and WAT increased in the SC group compared to other groups.
The findings demonstrate that six weeks of swimming training in cold water promotes additive effects of the expression of genes and proteins involved in the browning process of adipose tissue in Wistar rats. Myostatin inhibition may possess a regulator effect on the PGC-1α - UCP1 pathway that mediates adipose tissue browning.
棕色脂肪组织(BAT)是一种解耦氧化磷酸化和 ATP 合成的产热组织,通过非颤抖产热增加哺乳动物的能量消耗。冷暴露和运动已被证明可增加小鼠的 BAT 和白色脂肪组织(WAT)的褐变。本研究旨在确定在冷暴露期间运动是否对 Wistar 大鼠脂肪组织褐变相关标志物有相加作用。
将 24 只雄性 Wistar 大鼠随机分为三组:对照组(C,25°C)、中性水游泳组(SN,30°C)和冷水游泳组(SC,15°C)。游泳包括 2-3 分钟的间隔,1 分钟的休息,直到力竭,每周三天,持续六周,训练负荷为 3-6%体重。实验方案结束后,切除肩胛间 BAT 和腹股沟皮下白色脂肪组织(WAT),称重,并进行褐变标记基因表达处理。
SN 和 SC 导致体重增加减少,与 WAT 和 BAT 体积减少有关,BAT 数量增加,SC 组的效果更明显。BAT、WAT、比目鱼肌和血清中肌肉生长抑制素(Myostatin)蛋白表达水平低于 C 组。与 C 组相比,SC 组 BAT 和 WAT 组织中的干扰素调节因子-4(IRF4)基因表达显著增加。SC 组 BAT 中的过氧化物酶体增殖物激活受体-γ 共激活因子-1α(PGC-1α)表达显著增加,而 C 和 NC 组的 WAT 中表达增加。与其他组相比,SC 组 BAT 和 WAT 中的解偶联蛋白 1(UCP1)表达增加。
六周的冷水游泳训练可促进 Wistar 大鼠脂肪组织褐变过程中相关基因和蛋白表达的相加作用。肌肉生长抑制素的抑制可能对调节脂肪组织褐变的 PGC-1α-UCP1 途径具有调节作用。