Sex-dependent effects of a high-fat diet on the hypothalamic response in mice.

IF 4.9 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Virginie Dreux, Candice Lefebvre, Charles-Edward Breemeersch, Colin Salaün, Christine Bôle-Feysot, Charlène Guérin, Pierre Déchelotte, Alexis Goichon, Moïse Coëffier, Ludovic Langlois
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Abstract

Sex differences in rodent models of diet-induced obesity are still poorly documented, particularly regarding how central mechanisms vary between sexes in response to an obesogenic diet. Here, we wanted to determine whether obese phenotype and hypothalamic response to a high-fat diet (HFD) differed between male and female C57Bl/6J mice. Mice were exposed to either a 60% HFD or a standard diet first for both a long- (14 weeks) and shorter-periods of time (3, 7, 14 and 28 days). Analysis of the expression profile of key neuronal, glial and inflammatory hypothalamic markers was performed using RT-qPCR. In addition, astrocytic and microglial morphology was examined in the arcuate nucleus. Monitoring of body weight and composition revealed that body weight and fat mass gain appeared earlier and was more pronounced in male mice. After 14 weeks of HFD exposure, normalized increase of body weight reached similar levels between male and female mice. Overall, both sexes under HFD displayed a decrease of orexigenic neuropeptides expression while an increase in Pomc gene expression was observed only in female mice. In addition, changes in the expression of hypothalamic inflammatory markers were relatively modest. We also reported that the glial cell markers expression and morphology were affected by HFD in a sex- and time dependent manner, suggesting a more pronounced glial cell activation in female mice. Taken together, these data show that male and female mice responded differently to HFD exposure, both on short- and long-term and suggest that a strong inflammatory hypothalamic profile is not systematically present in diet-induced obesity models. Nevertheless, in addition to these present data, the underlying mechanisms should be deciphered in further investigations.

高脂肪饮食对小鼠下丘脑反应的性别依赖性影响。
啮齿类动物饮食性肥胖模型的性别差异仍然缺乏文献记载,特别是关于对致肥性饮食的反应中,不同性别的中枢机制是如何变化的。在这里,我们想要确定雄性和雌性C57Bl/6J小鼠的肥胖表型和对高脂肪饮食(HFD)的下丘脑反应是否不同。小鼠首先被暴露在60%高脂食物或标准饮食中,时间长(14周),时间短(3、7、14和28天)。采用RT-qPCR分析下丘脑关键神经元、胶质细胞和炎症标志物的表达谱。此外,还观察了弓形核的星形细胞和小胶质细胞形态。对体重和组成的监测显示,雄性小鼠的体重和脂肪量增加出现得更早,也更明显。暴露于HFD 14周后,雄性和雌性小鼠的正常体重增加达到相似的水平。总体而言,在HFD下,雌雄小鼠均表现出缺氧神经肽表达的减少,而Pomc基因表达的增加仅在雌性小鼠中观察到。此外,下丘脑炎症标志物的表达变化相对温和。我们还报道了HFD对神经胶质细胞标志物的表达和形态的影响,这种影响是性别和时间依赖的,这表明雌性小鼠的神经胶质细胞激活更为明显。综上所述,这些数据表明,无论是短期还是长期,雄性和雌性小鼠对HFD暴露的反应都是不同的,这表明在饮食诱导的肥胖模型中,强烈的下丘脑炎症并不系统地存在。然而,除了这些目前的数据,潜在的机制应该在进一步的调查中破译。
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来源期刊
Biology of Sex Differences
Biology of Sex Differences ENDOCRINOLOGY & METABOLISM-GENETICS & HEREDITY
CiteScore
12.10
自引率
1.30%
发文量
69
审稿时长
14 weeks
期刊介绍: Biology of Sex Differences is a unique scientific journal focusing on sex differences in physiology, behavior, and disease from molecular to phenotypic levels, incorporating both basic and clinical research. The journal aims to enhance understanding of basic principles and facilitate the development of therapeutic and diagnostic tools specific to sex differences. As an open-access journal, it is the official publication of the Organization for the Study of Sex Differences and co-published by the Society for Women's Health Research. Topical areas include, but are not limited to sex differences in: genomics; the microbiome; epigenetics; molecular and cell biology; tissue biology; physiology; interaction of tissue systems, in any system including adipose, behavioral, cardiovascular, immune, muscular, neural, renal, and skeletal; clinical studies bearing on sex differences in disease or response to therapy.
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