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间歇性禁食可上调白色脂肪组织中 Fsp27/Cidec 基因的表达。

Intermittent fasting up-regulates Fsp27/Cidec gene expression in white adipose tissue.

机构信息

Department of Biochemistry, Medical University of Gdansk, Gdansk, Poland.

出版信息

Nutrition. 2012 Mar;28(3):294-9. doi: 10.1016/j.nut.2011.06.009. Epub 2011 Oct 12.

Abstract

OBJECTIVE

Fat-specific protein of 27 kDa (FSP27) is a novel lipid droplet protein that promotes triacylglycerol storage in white adipose tissue (WAT). The regulation of the Fsp27 gene expression in WAT is largely unknown. We investigated the nutritional regulation of FSP27 in WAT.

METHODS

The effects of intermittent fasting (48 d, eight cycles of 3-d fasting and 3-d refeeding), caloric restriction (48 d), fasting-refeeding (3-d fasting and 3-d refeeding), and fasting (3 d) on mRNA expression of FSP27, peroxisome proliferator-activated receptor γ (PPARγ2), CCAAT/enhancer binding protein α (C/EBPα), and M isoform of carnitine palmitoyltransferase 1 (a positive control for PPARγ activation) in epididymal WAT and on serum triacylglycerol, insulin, and leptin levels were determined in Wistar rats. We also determined the effects of PPARγ activation by rosiglitazone or pioglitazone on FSP27 mRNA levels in primary rat adipocytes.

RESULTS

Long-term intermittent fasting, in contrast to other dietary manipulations, significantly up-regulated Fsp27 gene expression in WAT. Moreover, in rats subjected to intermittent fasting, serum insulin levels were elevated; PPARγ2 and C/EBPα mRNA expression in WAT was increased, and there was a positive correlation of Fsp27 gene expression with PPARγ2 and C/EBPα mRNA levels. FSP27 mRNA expression was also increased in adipocytes treated with PPARγ agonists.

CONCLUSION

Our study demonstrates that the transcription of the Fsp27 gene in adipose tissue may be induced in response to nutritional stimuli. Furthermore, PPARγ2, C/EBPα, and insulin may be involved in the nutritional regulation of FSP27. Thus intermittent fasting, despite lower caloric intake, may promote triacylglycerol deposition in WAT by increasing the expression of genes involved in lipid storage, such as Fsp27.

摘要

目的

27kDa 脂肪特异性蛋白(FSP27)是一种新型的脂滴蛋白,可促进白色脂肪组织(WAT)中三酰基甘油的储存。WAT 中 Fsp27 基因表达的调控尚不清楚。我们研究了 FSP27 在 WAT 中的营养调控。

方法

间歇性禁食(48d,8 个 3d 禁食和 3d 再喂养周期)、热量限制(48d)、禁食-再喂养(3d 禁食和 3d 再喂养)和禁食(3d)对附睾 WAT 中 FSP27、过氧化物酶体增殖物激活受体γ(PPARγ2)、CCAAT/增强子结合蛋白α(C/EBPα)和肉碱棕榈酰转移酶 1 的 M 同工型(PPARγ 激活的阳性对照)mRNA 表达的影响,并测定了 Wistar 大鼠血清三酰甘油、胰岛素和瘦素水平。我们还测定了 PPARγ 激动剂罗格列酮或吡格列酮对原代大鼠脂肪细胞中 FSP27 mRNA 水平的影响。

结果

与其他饮食处理相比,长期间歇性禁食显著上调了 WAT 中 Fsp27 基因的表达。此外,在间歇性禁食的大鼠中,血清胰岛素水平升高;WAT 中 PPARγ2 和 C/EBPα mRNA 表达增加,Fsp27 基因表达与 PPARγ2 和 C/EBPα mRNA 水平呈正相关。脂肪细胞中 PPARγ 激动剂的处理也增加了 FSP27 mRNA 的表达。

结论

本研究表明,脂肪组织中 Fsp27 基因的转录可能是对营养刺激的反应而诱导的。此外,PPARγ2、C/EBPα 和胰岛素可能参与了 FSP27 的营养调控。因此,尽管间歇性禁食的热量摄入较低,但通过增加参与脂质储存的基因(如 Fsp27)的表达,可能促进 WAT 中三酰基甘油的沉积。

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