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易肥胖和抗肥胖小鼠白色脂肪组织中响应高脂饮食和抗肥胖草药的差异蛋白质表达

Differential protein expression in white adipose tissue from obesity-prone and obesity-resistant mice in response to high fat diet and anti-obesity herbal medicines.

作者信息

Kim Sang Woo, Park Tae-Jun, Choi Jae Heon, Aseer Kanikkai Raja, Choi Ji-Young, Kim Ye Jin, Choi Myung-Sook, Yun Jong Won

机构信息

Department of Biotechnology, Daegu University, Kyungsan, Kyungbuk, Republic of Korea.

出版信息

Cell Physiol Biochem. 2015;35(4):1482-98. doi: 10.1159/000373967. Epub 2015 Mar 12.

Abstract

BACKGROUND

One of the most interesting issues in obesity research is why certain humans are obesity-prone (OP) while others are obesity-resistant (OR) upon exposure to a high-calorie diet. However, the pathways responsible for these phenotypic differences are still largely unknown.

METHODS

In order to discover marker molecules determining susceptibility and/or resistance to obesity in response to high fat diet (HFD) or anti-obesity herbal medicine (TH), we conducted comparative proteomic analysis of white adipose tissue (WAT) from OP, OR, as well as TH-treated mice.

RESULTS

OP mice fed HFD gained approximately 33% more body weight than OR mice, and TH significantly reduced body weight gain in HFD-fed mice by 30%. These mice were further subjected to proteomic analysis using two-dimensional electrophoresis (2-DE) combined with matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF-MS). Proteomic data revealed 59 spots that were differentially regulated from a total of 1,045 matched spots, and 57 spots of these were identified as altered WAT proteins between OP and OR mice by peptide mass finger printing. Interestingly, 45 proteins were similarly regulated in OR mice in response to TH treatment. Of these, 10 proteins have already been recognized in the context of obesity; however, other proteins involved in obesity susceptibility or resistance were identified for the first time in the present study.

CONCLUSION

Our results suggest that TH actively contributed to body weight reduction in HFD-fed obese mice by altering protein regulation in WAT, and it was also found that TH-responsive proteins can be used as potent molecules for obesity treatment.

摘要

背景

肥胖研究中最有趣的问题之一是,为什么有些人在接触高热量饮食时容易肥胖(OP),而另一些人则具有抗肥胖能力(OR)。然而,导致这些表型差异的途径在很大程度上仍然未知。

方法

为了发现决定对高脂肪饮食(HFD)或抗肥胖草药(TH)易感性和/或抗性的标记分子,我们对来自OP、OR以及经TH处理的小鼠的白色脂肪组织(WAT)进行了比较蛋白质组学分析。

结果

喂食HFD的OP小鼠比OR小鼠体重增加约33%,TH显著降低了喂食HFD小鼠的体重增加,降低了30%。这些小鼠进一步通过二维电泳(2-DE)结合基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)进行蛋白质组学分析。蛋白质组学数据显示,在总共1045个匹配点中有59个点受到差异调节,其中57个点通过肽质量指纹识别被鉴定为OP和OR小鼠之间WAT蛋白的改变。有趣的是,45种蛋白质在OR小鼠中对TH处理有类似的调节。其中,10种蛋白质在肥胖背景下已经被认识;然而,本研究首次鉴定了其他与肥胖易感性或抗性相关的蛋白质。

结论

我们的结果表明,TH通过改变WAT中的蛋白质调节,积极促进了喂食HFD的肥胖小鼠的体重减轻,并且还发现TH反应性蛋白可作为肥胖治疗的有效分子。

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