Non-obesogenic doses of palmitate disrupt circadian metabolism in adipocytes.

IF 3.5 4区 生物学 Q2 ENDOCRINOLOGY & METABOLISM
Yael Tal, Nava Chapnik, Oren Froy
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引用次数: 9

Abstract

Saturated fatty acids, such as palmitate, lead to circadian disruption. We aimed at studying the effect of low doses of palmitate on circadian metabolism and to decipher the mechanism by which fatty acids convey their effect in adipocytes. Mice were fed non-obesogenic doses of palm or olive oil and adipocytes were treated with palmitate and oleate. Cultured adipocytes treated with oleate showed increased AMPK activity and induced the expression of mitochondrial genes indicating increased fatty acid oxidation, while palmitate increased ACC activity and induced the expression of lipogenic genes, indicating increased fatty acid synthesis. Low doses of palmitate were sufficient to alter circadian rhythms, due to changes in the expression and/or activity of key metabolic proteins including GSK3β and AKT. Palmitate-induced AKT and GSK3β activation led to the phosphorylation of BMAL1 that resulted in low levels as well as high amplitude of circadian clock expression. In adipocytes, the detrimental metabolic alteration of palmitate manifests itself early on even at non-obesogenic levels. This is accompanied by modulating BMAL1 expression and phosphorylation levels, which lead to dampened clock gene expression.

非致肥剂量的棕榈酸酯会破坏脂肪细胞的昼夜代谢
饱和脂肪酸,如棕榈酸,会导致昼夜节律紊乱。我们旨在研究低剂量棕榈酸盐对昼夜节律代谢的影响,并破译脂肪酸在脂肪细胞中传递其作用的机制。给小鼠喂食非致肥胖剂量的棕榈油或橄榄油,并用棕榈酸盐和油酸盐处理脂肪细胞。用油酸处理的培养脂肪细胞显示出AMPK活性增加并诱导线粒体基因表达,表明脂肪酸氧化增加,而棕榈酸增加ACC活性并诱导脂肪生成基因表达,表示脂肪酸合成增加。由于关键代谢蛋白(包括GSK3β和AKT)的表达和/或活性发生变化,低剂量的棕榈酸盐足以改变昼夜节律。棕榈酸酯诱导的AKT和GSK3β激活导致BMAL1的磷酸化,导致昼夜节律时钟表达的低水平和高幅度。在脂肪细胞中,棕榈酸的有害代谢变化在早期就表现出来,即使在非肥胖水平上也是如此。这伴随着调节BMAL1的表达和磷酸化水平,导致时钟基因表达减弱。
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来源期刊
Adipocyte
Adipocyte Medicine-Histology
CiteScore
6.50
自引率
3.00%
发文量
46
审稿时长
32 weeks
期刊介绍: Adipocyte recognizes that the adipose tissue is the largest endocrine organ in the body, and explores the link between dysfunctional adipose tissue and the growing number of chronic diseases including diabetes, hypertension, cardiovascular disease and cancer. Historically, the primary function of the adipose tissue was limited to energy storage and thermoregulation. However, a plethora of research over the past 3 decades has recognized the dynamic role of the adipose tissue and its contribution to a variety of physiological processes including reproduction, angiogenesis, apoptosis, inflammation, blood pressure, coagulation, fibrinolysis, immunity and general metabolic homeostasis. The field of Adipose Tissue research has grown tremendously, and Adipocyte is the first international peer-reviewed journal of its kind providing a multi-disciplinary forum for research focusing exclusively on all aspects of adipose tissue physiology and pathophysiology. Adipocyte accepts high-profile submissions in basic, translational and clinical research.
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