Reynés Bàrbara, Klein Hazebroek Marlou, García-Ruiz Estefanía, Keijer Jaap, Oliver Paula, Palou Andreu
Laboratory of Molecular Biology, Nutrition, and Biotechnology, Universitat de les Illes BalearsPalma, Spain.
CIBER de Fisiopatología de la Obesidad y Nutrición (CIBERobn)Palma, Spain.
Front Physiol. 2017 Aug 15;8:581. doi: 10.3389/fphys.2017.00581. eCollection 2017.
Cold exposure induces hyperphagia to counteract fat loss related to lipid mobilization and thermogenic activation. The aim of this study was investigate on the molecular mechanisms involved in cold-induced compensatory hyperphagia. We analyzed the effect of cold exposure on gene expression of orexigenic and anorexigenic peptides, and of leptin signaling-related genes in the hypothalamus of rats at different ages (1, 2, 4, and 6 months), as well as in ferrets. We also evaluated the potential of peripheral blood mononuclear cells to reflect hypothalamic molecular responses. As expected, cold exposure induced hypoleptinemia in rats, which could be responsible for the increased ratio of orexigenic/anorexigenic peptides gene expression in the hypothalamus, mainly due to decreased anorexigenic gene expression, especially in young animals. In ferrets, which resemble humans more closely, cold exposure induced greater changes in hypothalamic mRNA levels of orexigenic genes. Despite the key role of leptin in food intake control, the effect of cold exposure on the expression of key hypothalamic leptin signaling cascade genes is not clear. In our study, cold exposure seemed to affect leptin signaling in 4-month-old rats (increased and expression), likely associated with the smaller-increase in food intake and decreased body weight observed at this particular age. Similarly, cold exposed ferrets showed greater hypothalamic and gene expression. Interestingly, peripheral blood mononuclear cells (PBMC) mimicked the hypothalamic increase in and observed in 4-month-old rats, and the increased mRNA expression observed in ferrets in response to cold exposure. The most outstanding result of our study is that PBMC reflected the specific modulation of leptin signaling observed in both animal models, rats and ferrets, which points forwards PBMC as easily obtainable biological material to be considered as a potential surrogate tissue to perform further studies on the regulation of hypothalamic leptin signaling in response to cold exposure.
寒冷暴露会引发食欲亢进,以抵消与脂质动员和产热激活相关的脂肪损失。本研究的目的是探讨寒冷诱导的代偿性食欲亢进所涉及的分子机制。我们分析了寒冷暴露对不同年龄(1、2、4和6个月)大鼠以及雪貂下丘脑内食欲肽和厌食肽基因表达以及瘦素信号相关基因表达的影响。我们还评估了外周血单核细胞反映下丘脑分子反应的潜力。正如预期的那样,寒冷暴露导致大鼠瘦素血症降低,这可能是下丘脑内食欲肽/厌食肽基因表达比例增加的原因,主要是由于厌食基因表达减少,尤其是在幼龄动物中。在与人类更相似的雪貂中,寒冷暴露导致下丘脑食欲基因的mRNA水平发生更大变化。尽管瘦素在食物摄入控制中起关键作用,但寒冷暴露对下丘脑关键瘦素信号级联基因表达的影响尚不清楚。在我们的研究中,寒冷暴露似乎影响4个月龄大鼠的瘦素信号(增加 和 表达),这可能与该特定年龄观察到的食物摄入量增加较小和体重减轻有关。同样,寒冷暴露的雪貂显示下丘脑 和 基因表达增加。有趣的是,外周血单核细胞(PBMC)模拟了4个月龄大鼠下丘脑内 和 的增加,以及雪貂中观察到的因寒冷暴露而导致的 mRNA表达增加。我们研究中最突出的结果是,PBMC反映了在大鼠和雪貂这两种动物模型中观察到的瘦素信号的特定调节,这表明PBMC作为一种易于获取的生物材料,可被视为潜在的替代组织,用于进一步研究寒冷暴露对下丘脑瘦素信号调节的影响。