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CD1 参与肥胖症引起的下丘脑炎症。

CD1 is involved in diet-induced hypothalamic inflammation in obesity.

机构信息

Laboratory of Cell Signaling, University of Campinas, Campinas, São Paulo 13084-970, Brazil.

Laboratory of Molecular Biology of Exercise, University of Campinas (UNICAMP), Limeira, São Paulo, Brazil.

出版信息

Brain Behav Immun. 2019 May;78:78-90. doi: 10.1016/j.bbi.2019.01.011. Epub 2019 Jan 17.

Abstract

Obesity-associated hypothalamic inflammation plays an important role in the development of defective neuronal control of whole body energy balance. Because dietary fats are the main triggers of hypothalamic inflammation, we hypothesized that CD1, a lipid-presenting protein, may be involved in the hypothalamic inflammatory response in obesity. Here, we show that early after the introduction of a high-fat diet, CD1 expressing cells gradually appear in the mediobasal hypothalamus. The inhibition of hypothalamic CD1 reduces diet-induced hypothalamic inflammation and rescues the obese and glucose-intolerance phenotype of mice fed a high-fat diet. Conversely, the chemical activation of hypothalamic CD1 further increases diet-induced obesity and hypothalamic inflammation. A bioinformatics analysis revealed that hypothalamic CD1 correlates with transcripts encoding for proteins known to be involved in diet-induced hypothalamic abnormalities in obesity. Thus, CD1 is involved in at least part of the hypothalamic inflammatory response in diet-induced obesity and its modulation affects the body mass phenotype of mice.

摘要

肥胖相关的下丘脑炎症在全身能量平衡的神经元控制缺陷的发展中起着重要作用。因为膳食脂肪是下丘脑炎症的主要触发因素,我们假设 CD1,一种脂质呈递蛋白,可能参与肥胖症中的下丘脑炎症反应。在这里,我们发现,在高脂肪饮食引入后的早期,CD1 表达细胞逐渐出现在下丘脑中间基底部。抑制下丘脑 CD1 可减少饮食诱导的下丘脑炎症,并挽救高脂肪饮食喂养的肥胖和葡萄糖不耐受表型的小鼠。相反,化学激活下丘脑 CD1 会进一步增加饮食诱导的肥胖和下丘脑炎症。生物信息学分析显示,下丘脑 CD1 与编码已知参与肥胖症中饮食诱导的下丘脑异常的蛋白质的转录本相关。因此,CD1 至少参与了饮食诱导肥胖症中的部分下丘脑炎症反应,其调节作用会影响小鼠的体重表型。

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