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他莫昔芬通过增加活性氧来减少脂肪量。

Tamoxifen reduces fat mass by boosting reactive oxygen species.

作者信息

Liu L, Zou P, Zheng L, Linarelli L E, Amarell S, Passaro A, Liu D, Cheng Z

机构信息

Department of Human Nutrition, Foods and Exercise, Fralin Life Science Institute, College of Agriculture and Life Science, Virginia Tech, Blacksburg, VA, USA.

出版信息

Cell Death Dis. 2015 Jan 8;6(1):e1586. doi: 10.1038/cddis.2014.553.

Abstract

As the pandemic of obesity is growing, a variety of animal models have been generated to study the mechanisms underlying the increased adiposity and development of metabolic disorders. Tamoxifen (Tam) is widely used to activate Cre recombinase that spatiotemporally controls target gene expression and regulates adiposity in laboratory animals. However, a critical question remains as to whether Tam itself affects adiposity and possibly confounds the functional study of target genes in adipose tissue. Here we administered Tam to Cre-absent forkhead box O1 (FoxO1) floxed mice (f-FoxO1) and insulin receptor substrate Irs1/Irs2 double floxed mice (df-Irs) and found that Tam induced approximately 30% reduction (P<0.05) in fat mass with insignificant change in body weight. Mechanistically, Tam promoted reactive oxygen species (ROS) production, apoptosis and autophagy, which was associated with downregulation of adipogenic regulator peroxisome proliferator-activated receptor gamma and dedifferentiation of mature adipocytes. However, normalization of ROS potently suppressed Tam-induced apoptosis, autophagy and adipocyte dedifferentiation, suggesting that ROS may account, at least in part, for the changes. Importantly, Tam-induced ROS production and fat mass reduction lasted for 4-5 weeks in the f-FoxO1 and df-Irs mice. Our data suggest that Tam reduces fat mass via boosting ROS, thus making a recovery period crucial for posttreatment study.

摘要

随着肥胖症大流行的加剧,人们建立了多种动物模型来研究肥胖增加和代谢紊乱发展的潜在机制。他莫昔芬(Tam)被广泛用于激活Cre重组酶,该酶可时空控制靶基因表达并调节实验动物的肥胖状况。然而,一个关键问题仍然存在,即Tam本身是否会影响肥胖,是否可能混淆脂肪组织中靶基因的功能研究。在此,我们对缺乏Cre的叉头框O1(FoxO1)基因敲除小鼠(f-FoxO1)和胰岛素受体底物Irs1/Irs2双基因敲除小鼠(df-Irs)给予Tam,发现Tam使脂肪量减少了约30%(P<0.05),而体重变化不显著。从机制上讲,Tam促进活性氧(ROS)生成、细胞凋亡和自噬,这与脂肪生成调节因子过氧化物酶体增殖物激活受体γ的下调以及成熟脂肪细胞的去分化有关。然而,ROS的正常化有力地抑制了Tam诱导的细胞凋亡、自噬和脂肪细胞去分化,这表明ROS可能至少部分地解释了这些变化。重要的是,在f-FoxO1和df-Irs小鼠中,Tam诱导的ROS生成和脂肪量减少持续了4至5周。我们的数据表明,Tam通过增强ROS来减少脂肪量,因此恢复期对于治疗后研究至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e78/4669751/075ade1df375/cddis2014553f1.jpg

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