期刊文献+

转录因子FoxO1在糖脂代谢及肥胖症中的研究进展 被引量:2

Research Progress of Transcription Factor FoxO1 in Glycolipid Metabolism and Obesity
下载PDF
导出
摘要 叉头框转录因子O亚型1(FoxO1)作为人体重要的转录因子,参与细胞代谢、生长、分化、氧化应激、衰老、自噬等多种生理和病理过程,其转录活性受多个上游通路翻译后修饰和细胞核-质异位调节。FoxO1基因突变或蛋白异常表达在糖脂代谢及肥胖症等代谢性疾病的发生发展中起重要作用。目前代谢性疾病发病率高且控制欠佳,除饮食及运动外,无特效药。FoxO1在改善胰岛β细胞功能、改善胰岛素抵抗以及纠正脂代谢紊乱、干预肥胖症等方面发挥作用。因此,FoxO1可能为糖脂代谢及肥胖症的治疗提供新思路。 As an important transcription factor in human body,the forkhead box O1(FoxO1),is involved in a variety of physiological and pathological processes such as cell metabolism,growth,differentiation,oxidative stress,aging,autophagy,and so on.Its transcriptional activity is regulated by post-translational modification of multiple upstream pathways and nuclear-plasmid ectopia.FoxO1 gene mutation or abnormal protein expression plays an important role in the occurrence and development of metabolic diseases such as glucose and lipid metabolism and obesity.At present,the incidence of the metabolic diseases is high incidence and is poorly controlled.Except diet and exercise,there is no specific medicine.FoxO1 plays a role in improving the function of islet cells,improving insulin resistance,correcting the disorder of lipid metabolism,and intervening obesity.Therefore,FoxO1 may provide new ideas for the treatment of glucose and lipid metabolism and obesity.
作者 耿丽莎 何军华 GENG Lisha;HE Junhua(Department of Endocrinology,the Second Hospital of Shanxi Medical University,Taiyuan 030001,China)
出处 《医学综述》 2020年第24期4927-4931,共5页 Medical Recapitulate
基金 山西省回国留学人员科研资助项目(2017-117) 山西省留学人员科技活动择优资助项目(晋人社厅函〔2017〕1389号) 山西省高校“131”领军人才工程项目(晋教财〔2015〕41号)。
关键词 高脂血症 肥胖症 叉头转录因子O亚型1 胰岛Β细胞 胰岛素抵抗 Hyperlipidemia Obesity Forkhead box protein O1 Isletβcell Insulin resistance
  • 相关文献

参考文献1

二级参考文献36

  • 1American Diabetes Association.Diagnosis and classification of diabetes mellitus.Diabetes Care 2012,35(Suppl 1):S64-S71.
  • 2Wild S,Roglic G,Green A,Sicree R and King H.Global prevalence of dia-betes:estimates for the year 2000 and projections for 2030.Diabetes Care 2004,27:1047-1053.
  • 3Giacco F and Brownlee M.Oxidative stress and diabetic complications.Circ Res 2010,107:1058-1070.
  • 4Rains JL and Jain SK.Oxidative stress,insulin signaling,and diabetes.Free Radic Biol Med 2011,50:567-575.
  • 5Pitocco D,Zaccardi F,Di Stasio E,Romitelli F,Santini SA,Zuppi C and Ghirlanda G.Oxidative stress,nitric oxide,and diabetes.Rev Diabet Stud 2010,7:15-25.
  • 6Singh DK,Winocour P and Farrington K.Oxidative stress in early diabetic nephropathy:fueling the fire.Nat Rev Endocrinol 2011,7:176-184.
  • 7Folli F,Corradi D,Fanti P,Davalli A,Paez A,Giaccari A and Perego C,et al.The role of oxidative stress in the pathogenesis of type 2 diabetes mel-litus micro-and macrovascular complications:avenues for a mechanistic-based therapeutic approach.Curr Diabetes Rev 2011,7:313-324.
  • 8Storz P.Forkhead homeobox type O transcription factors in the responses to oxidative stress.Antioxid Redox Signal 2011,14:593-605.
  • 9Evans JL,Goldfine 1D,Maddux BA and Grodsky GM.Are oxidative stress-activated signaling pathways mediators of insulin resistance and beta-cell dysfunction? Diabetes 2003,52:1-8.
  • 10Newsholme it',Rebelato E,Abdulkader E Krause M,Carpinelli A and Curi R.Reactive oxygen and nitrogen species generation,antioxidant defenses,and 13-cell function:a critical role for amino acids.J Endocrino12012,214:11-20.

共引文献4

同被引文献12

引证文献2

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部