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本文引用的文献

1
Glucose-6-Phosphate Dehydrogenase Deficiency Improves Insulin Resistance With Reduced Adipose Tissue Inflammation in Obesity.葡萄糖-6-磷酸脱氢酶缺乏症可改善肥胖症中的胰岛素抵抗并减轻脂肪组织炎症。
Diabetes. 2016 Sep;65(9):2624-38. doi: 10.2337/db16-0060. Epub 2016 Jun 9.
2
G6PD protects from oxidative damage and improves healthspan in mice.葡萄糖-6-磷酸脱氢酶(G6PD)可保护小鼠免受氧化损伤并改善其健康寿命。
Nat Commun. 2016 Mar 15;7:10894. doi: 10.1038/ncomms10894.
3
Hypoxia-induced glucose-6-phosphate dehydrogenase overexpression and -activation in pulmonary artery smooth muscle cells: implication in pulmonary hypertension.低氧诱导肺动脉平滑肌细胞葡萄糖-6-磷酸脱氢酶过表达和激活:在肺动脉高压中的意义。
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4
Oxidative stress and metabolic pathologies: from an adipocentric point of view.氧化应激与代谢性疾病:以脂肪为中心的视角
Oxid Med Cell Longev. 2014;2014:908539. doi: 10.1155/2014/908539. Epub 2014 Jul 20.
5
Transcriptional and epigenetic basis for restoration of G6PD enzymatic activity in human G6PD-deficient cells.人类 G6PD 缺乏细胞中 G6PD 酶活性恢复的转录和表观遗传基础。
Blood. 2014 Jul 3;124(1):134-41. doi: 10.1182/blood-2014-02-553792. Epub 2014 May 7.
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Crosstalk between adipocytes and immune cells in adipose tissue inflammation and metabolic dysregulation in obesity.肥胖中脂肪组织炎症和代谢失调时脂肪细胞与免疫细胞之间的相互作用。
Mol Cells. 2014 May;37(5):365-71. doi: 10.14348/molcells.2014.0074. Epub 2014 Apr 30.
7
Modulation of oxidative stress as an anticancer strategy.氧化应激调节作为一种抗癌策略。
Nat Rev Drug Discov. 2013 Dec;12(12):931-47. doi: 10.1038/nrd4002.
8
Macrophage glucose-6-phosphate dehydrogenase stimulates proinflammatory responses with oxidative stress.巨噬细胞葡萄糖-6-磷酸脱氢酶通过氧化应激刺激促炎反应。
Mol Cell Biol. 2013 Jun;33(12):2425-35. doi: 10.1128/MCB.01260-12. Epub 2013 Apr 9.
9
Impact of glucose-6-phosphate dehydrogenase deficiency on the pathophysiology of cardiovascular disease.葡萄糖-6-磷酸脱氢酶缺乏症对心血管疾病病理生理学的影响。
Am J Physiol Heart Circ Physiol. 2013 Feb 15;304(4):H491-500. doi: 10.1152/ajpheart.00721.2012. Epub 2012 Dec 15.
10
Cytosolic malic enzyme 1 (ME1) mediates high fat diet-induced adiposity, endocrine profile, and gastrointestinal tract proliferation-associated biomarkers in male mice.细胞质苹果酸酶 1(ME1)介导高脂肪饮食诱导的雄性小鼠肥胖、内分泌特征和胃肠道增殖相关生物标志物。
PLoS One. 2012;7(10):e46716. doi: 10.1371/journal.pone.0046716. Epub 2012 Oct 4.

葡萄糖-6-磷酸脱氢酶在肥胖症脂肪组织炎症中的作用。

The role of glucose-6-phosphate dehydrogenase in adipose tissue inflammation in obesity.

作者信息

Park Yoon Jeong, Choe Sung Sik, Sohn Jee Hyung, Kim Jae Bum

机构信息

a Department of Biological Science , Institute of Molecular Biology & Genetics, Seoul National University , Seoul , Korea.

b Department of Biophysics and Chemical Biology , Seoul National University , Seoul , Korea.

出版信息

Adipocyte. 2017 Apr 3;6(2):147-153. doi: 10.1080/21623945.2017.1288321. Epub 2017 Feb 8.

DOI:10.1080/21623945.2017.1288321
PMID:28425844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5477698/
Abstract

Obesity is closely associated with metabolic diseases including type 2 diabetes. One hallmark characteristics of obesity is chronic inflammation that is coordinately controlled by complex signaling networks in adipose tissues. Compelling evidence indicates that reactive oxygen species (ROS) and its related signaling pathways play crucial roles in the progression of chronic inflammation in obesity. The pentose phosphate pathway (PPP) is an anabolic pathway that utilizes the glucoses to generate molecular building blocks and reducing equivalents in the form of NADPH. In particular, NADPH acts as one of the key modulators in the control of ROS through providing an electron for both ROS generation and scavenging. Recently, we have reported that glucose-6-phosphate dehydrogenase (G6PD), a rate-limiting enzyme of the PPP, is implicated in adipose tissue inflammation and systemic insulin resistance in obesity. Mechanistically, G6PD potentiates generation of ROS that augments pro-inflammatory responses in adipose tissue macrophages, leading to systemic insulin resistance. Here, we provide an overview of cell type- specific roles of G6PD in the regulation of ROS balance as well as additional details on the significance of G6PD that contributes to pro-oxidant NADPH generation in obesity-related chronic inflammation and insulin resistance.

摘要

肥胖与包括2型糖尿病在内的代谢性疾病密切相关。肥胖的一个标志性特征是慢性炎症,它由脂肪组织中的复杂信号网络协同控制。有力证据表明,活性氧(ROS)及其相关信号通路在肥胖相关慢性炎症的进展中起关键作用。磷酸戊糖途径(PPP)是一种合成代谢途径,利用葡萄糖生成分子构件并以NADPH的形式产生还原当量。特别是,NADPH通过为ROS的产生和清除提供电子,作为控制ROS的关键调节因子之一。最近,我们报道了PPP的限速酶葡萄糖-6-磷酸脱氢酶(G6PD)与肥胖中的脂肪组织炎症和全身胰岛素抵抗有关。从机制上讲,G6PD增强ROS的产生,从而增强脂肪组织巨噬细胞中的促炎反应,导致全身胰岛素抵抗。在这里,我们概述了G6PD在调节ROS平衡中的细胞类型特异性作用,以及G6PD在肥胖相关慢性炎症和胰岛素抵抗中促进促氧化NADPH生成的重要性的更多细节。