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水动力递送 mIL10 基因可保护小鼠免受高脂肪饮食诱导的肥胖和葡萄糖不耐受。

Hydrodynamic delivery of mIL10 gene protects mice from high-fat diet-induced obesity and glucose intolerance.

机构信息

Department of Pharmaceutical and Biomedical Sciences, College of Pharmacy, University of Georgia, Athens, Georgia, USA.

出版信息

Mol Ther. 2013 Oct;21(10):1852-61. doi: 10.1038/mt.2013.125. Epub 2013 Jun 18.

DOI:10.1038/mt.2013.125
PMID:23774795
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3808131/
Abstract

High-fat diet (HFD) induced obesity is associated with low-grade inflammation, insulin resistance (IR), and glucose intolerance. The objective of this study is to assess the effect of interleukin 10 (IL10), an anti-inflammatory cytokine, on blocking HFD-induced obesity and obesity-associated metabolic disorders by hydrodynamic delivery of IL10-containing plasmid. Animals fed a regular chow or HFD received two injections (one on day 1 and the other on day 31) of plasmids containing green fluorescence protein (GFP) or mouse IL10 (mIL10) gene. Blood concentration of mIL10 reached ~200 ng/ml on day 7 in animals receiving mIL10 plasmid DNA. The transfection efficiency of liver cells was the same in animals fed a regular chow or HFD. No difference was seen in animals on regular chow when injected with plasmids containing either gfp or mIL10 gene. Overexpression of mIL10 prevented weight gain of animals on HFD. Intraperitoneal glucose tolerance test (IPGTT) and insulin tolerance tests (ITT) showed that mIL10 maintained insulin sensitivity and prevented glucose intolerance. The mechanistic study reveals that mIL10 suppressed macrophage infiltration and reduced the development of crown-like structures in adipose tissue (AT). Collectively, these results suggest that maintaining a higher level of IL10 through gene transfer could be an effective strategy in preventing diet-induced obesity.

摘要

高脂肪饮食(HFD)诱导的肥胖与低度炎症、胰岛素抵抗(IR)和葡萄糖耐量降低有关。本研究的目的是通过水动力传递含有白细胞介素 10(IL10)的质粒,评估抗炎细胞因子 IL10 对阻止 HFD 诱导的肥胖和肥胖相关代谢紊乱的作用。给予常规饲料或 HFD 的动物接受两次注射(一次在第 1 天,另一次在第 31 天),分别含有绿色荧光蛋白(GFP)或小鼠 IL10(mIL10)基因的质粒。接受 mIL10 质粒 DNA 的动物在第 7 天血液中 mIL10 浓度达到约 200ng/ml。在给予常规饲料或 HFD 的动物中,肝细胞的转染效率相同。在给予常规饲料的动物中,注射含有 GFP 或 mIL10 基因的质粒没有差异。在 HFD 喂养的动物中过表达 mIL10 可防止体重增加。腹腔内葡萄糖耐量试验(IPGTT)和胰岛素耐量试验(ITT)表明,mIL10 保持了胰岛素敏感性并防止了葡萄糖耐量降低。机制研究表明,mIL10 抑制了巨噬细胞浸润并减少了脂肪组织(AT)中冠状结构的形成。总之,这些结果表明,通过基因转移维持更高水平的 IL10 可能是预防饮食诱导肥胖的有效策略。

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PLoS One. 2012;7(12):e53154. doi: 10.1371/journal.pone.0053154. Epub 2012 Dec 28.
2
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Nat Rev Drug Discov. 2012 Sep;11(9):675-91. doi: 10.1038/nrd3739. Epub 2012 Aug 3.
3
Inflammasome-mediated dysbiosis regulates progression of NAFLD and obesity.炎症小体介导的微生态失调调控非酒精性脂肪性肝病和肥胖的进展。
Nature. 2012 Feb 1;482(7384):179-85. doi: 10.1038/nature10809.
4
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5
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6
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N Engl J Med. 2011 Mar 17;364(11):987-9. doi: 10.1056/NEJMp1009229.
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