• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

小干扰RNA揭示人骨骼肌中胰岛素信号传导的特异性

Specificity of insulin signalling in human skeletal muscle as revealed by small interfering RNA.

作者信息

Krook A, Zierath J R

机构信息

Department of Molecular Medicine and Surgery, Section of Integrative Physiology, Karolinska Institutet, von Eulers väg 4, Stockholm, Sweden.

出版信息

Diabetologia. 2009 Jul;52(7):1231-9. doi: 10.1007/s00125-009-1330-y. Epub 2009 Mar 31.

DOI:10.1007/s00125-009-1330-y
PMID:19333572
Abstract

Insulin action on metabolically active tissues is a complex process involving positive and negative feedback regulation to control whole body glucose homeostasis. At the cellular level, glucose and lipid metabolism, as well as protein synthesis, are controlled through canonical insulin signalling cascades. The discovery of small interfering RNA (siRNA) allows for the molecular dissection of critical components of the regulation of metabolic and gene regulatory events in insulin-sensitive tissues. The application of siRNA to tissues of human origin allows for the molecular dissection of the mechanism(s) regulating glucose and lipid metabolism. Penetration of the pathways controlling insulin action in human tissue may aid in discovery efforts to develop diabetes prevention and treatment strategies. This review will focus on the use of siRNA to validate critical regulators controlling insulin action in human skeletal muscle, a key organ important for the control of whole body insulin-mediated glucose uptake and metabolism.

摘要

胰岛素对代谢活跃组织的作用是一个复杂的过程,涉及正负反馈调节,以控制全身葡萄糖稳态。在细胞水平上,葡萄糖和脂质代谢以及蛋白质合成是通过经典的胰岛素信号级联反应来控制的。小干扰RNA(siRNA)的发现使得对胰岛素敏感组织中代谢和基因调控事件调节的关键成分进行分子剖析成为可能。将siRNA应用于人类来源的组织有助于对调节葡萄糖和脂质代谢的机制进行分子剖析。深入了解控制人体组织中胰岛素作用的途径可能有助于发现预防和治疗糖尿病的策略。本综述将重点关注使用siRNA来验证控制人类骨骼肌中胰岛素作用的关键调节因子,骨骼肌是控制全身胰岛素介导的葡萄糖摄取和代谢的重要关键器官。

相似文献

1
Specificity of insulin signalling in human skeletal muscle as revealed by small interfering RNA.小干扰RNA揭示人骨骼肌中胰岛素信号传导的特异性
Diabetologia. 2009 Jul;52(7):1231-9. doi: 10.1007/s00125-009-1330-y. Epub 2009 Mar 31.
2
Metabolism and insulin signaling in common metabolic disorders and inherited insulin resistance.常见代谢紊乱和遗传性胰岛素抵抗中的代谢与胰岛素信号传导
Dan Med J. 2014 Jul;61(7):B4890.
3
From receptor to effector: insulin signal transduction in skeletal muscle from type II diabetic patients.从受体到效应器:II型糖尿病患者骨骼肌中的胰岛素信号转导
Ann N Y Acad Sci. 2002 Jun;967:120-34. doi: 10.1111/j.1749-6632.2002.tb04270.x.
4
Insulin signal transduction in human skeletal muscle: identifying the defects in Type II diabetes.人类骨骼肌中的胰岛素信号转导:识别2型糖尿病中的缺陷。
Biochem Soc Trans. 2005 Apr;33(Pt 2):354-7. doi: 10.1042/BST0330354.
5
Insulin signaling and glucose transport in insulin resistant human skeletal muscle.胰岛素抵抗的人体骨骼肌中的胰岛素信号传导与葡萄糖转运
Cell Biochem Biophys. 2007;48(2-3):103-13. doi: 10.1007/s12013-007-0030-9.
6
siRNA-based gene silencing reveals specialized roles of IRS-1/Akt2 and IRS-2/Akt1 in glucose and lipid metabolism in human skeletal muscle.基于小干扰RNA的基因沉默揭示了胰岛素受体底物-1/蛋白激酶B2和胰岛素受体底物-2/蛋白激酶B1在人类骨骼肌葡萄糖和脂质代谢中的特殊作用。
Cell Metab. 2006 Jul;4(1):89-96. doi: 10.1016/j.cmet.2006.04.008.
7
Intracellular mechanisms underlying increases in glucose uptake in response to insulin or exercise in skeletal muscle.骨骼肌中响应胰岛素或运动时葡萄糖摄取增加的细胞内机制。
Acta Physiol Scand. 2001 Mar;171(3):249-57. doi: 10.1046/j.1365-201x.2001.00827.x.
8
Regulation of glucose transport in human skeletal muscle.人类骨骼肌中葡萄糖转运的调节
Ann Med. 2002;34(6):410-8. doi: 10.1080/078538902321012351.
9
MicroRNA-194 Modulates Glucose Metabolism and Its Skeletal Muscle Expression Is Reduced in Diabetes.微小RNA-194调节葡萄糖代谢,且其在骨骼肌中的表达在糖尿病中降低。
PLoS One. 2016 May 10;11(5):e0155108. doi: 10.1371/journal.pone.0155108. eCollection 2016.
10
Regulation of skeletal muscle sucrose, non-fermenting 1/AMP-activated protein kinase-related kinase (SNARK) by metabolic stress and diabetes.代谢应激和糖尿病对骨骼肌蔗糖非发酵1/AMP激活蛋白激酶相关激酶(SNARK)的调节作用
Diabetologia. 2009 Oct;52(10):2182-9. doi: 10.1007/s00125-009-1465-x. Epub 2009 Aug 4.

引用本文的文献

1
The impact of ncRNAs on type 2 diabetes: A comprehensive review covering molecular mechanisms to clinical applications.非编码RNA对2型糖尿病的影响:从分子机制到临床应用的全面综述
Mol Ther Nucleic Acids. 2025 Jul 17;36(3):102629. doi: 10.1016/j.omtn.2025.102629. eCollection 2025 Sep 9.
2
Insulin Receptor Substrate 1 Signaling Inhibits Foxp3 Expression and Suppressive Functions in Treg Cells through the mTORC1 Pathway.胰岛素受体底物 1 信号通过 mTORC1 通路抑制调节性 T 细胞中 Foxp3 的表达和抑制功能。
Int J Mol Sci. 2023 Jan 29;24(3):2551. doi: 10.3390/ijms24032551.
3
Activation of Insulin Signaling in Adipocytes and Myotubes by Extract.

本文引用的文献

1
The promises and pitfalls of RNA-interference-based therapeutics.基于RNA干扰疗法的前景与隐患
Nature. 2009 Jan 22;457(7228):426-33. doi: 10.1038/nature07758.
2
Development of a novel GLUT4 translocation assay for identifying potential novel therapeutic targets for insulin sensitization.开发一种新型葡萄糖转运蛋白4(GLUT4)转位检测方法,用于鉴定胰岛素增敏潜在的新型治疗靶点。
Biochem J. 2009 Mar 1;418(2):413-20. doi: 10.1042/BJ20082051.
3
Insulin sensitivity: modulation by nutrients and inflammation.胰岛素敏感性:受营养物质和炎症的调节
提取物对脂肪细胞和肌管中胰岛素信号的激活作用。
Nutrients. 2019 Jun 21;11(6):1396. doi: 10.3390/nu11061396.
4
A novel method to measure glucose uptake and myosin heavy chain isoform expression of single fibers from rat skeletal muscle.一种测量大鼠骨骼肌单纤维葡萄糖摄取和肌球蛋白重链同工型表达的新方法。
Diabetes. 2012 May;61(5):995-1003. doi: 10.2337/db11-1299. Epub 2012 Mar 6.
5
Inhibitory effect of the D(3) dopamine receptor on insulin receptor expression and function in vascular smooth muscle cells.D3 多巴胺受体对血管平滑肌细胞胰岛素受体表达和功能的抑制作用。
Am J Hypertens. 2011 Jun;24(6):654-60. doi: 10.1038/ajh.2011.41. Epub 2011 Mar 17.
J Clin Invest. 2008 Sep;118(9):2992-3002. doi: 10.1172/JCI34260.
4
Phosphorylation of IRS proteins, insulin action, and insulin resistance.胰岛素受体底物蛋白的磷酸化、胰岛素作用及胰岛素抵抗
Am J Physiol Endocrinol Metab. 2009 Apr;296(4):E581-91. doi: 10.1152/ajpendo.90437.2008. Epub 2008 Aug 26.
5
Pathogenesis of type 2 diabetes: tracing the reverse route from cure to cause.2型糖尿病的发病机制:追溯从治愈到病因的反向路径。
Diabetologia. 2008 Oct;51(10):1781-9. doi: 10.1007/s00125-008-1116-7. Epub 2008 Aug 26.
6
The role of insulin receptor signaling in zebrafish embryogenesis.胰岛素受体信号在斑马鱼胚胎发育中的作用。
Endocrinology. 2008 Dec;149(12):5996-6005. doi: 10.1210/en.2008-0329. Epub 2008 Aug 7.
7
siRNA-mediated reduction of inhibitor of nuclear factor-kappaB kinase prevents tumor necrosis factor-alpha-induced insulin resistance in human skeletal muscle.小干扰RNA介导的核因子-κB激酶抑制剂的减少可预防肿瘤坏死因子-α诱导的人骨骼肌胰岛素抵抗。
Diabetes. 2008 Aug;57(8):2066-73. doi: 10.2337/db07-0763. Epub 2008 Apr 28.
8
Adipocyte dysfunctions linking obesity to insulin resistance and type 2 diabetes.将肥胖与胰岛素抵抗及2型糖尿病联系起来的脂肪细胞功能障碍。
Nat Rev Mol Cell Biol. 2008 May;9(5):367-77. doi: 10.1038/nrm2391.
9
Structural and biochemical characterization of the KRLB region in insulin receptor substrate-2.胰岛素受体底物-2中KRLB区域的结构与生化特性
Nat Struct Mol Biol. 2008 Mar;15(3):251-8. doi: 10.1038/nsmb.1388. Epub 2008 Feb 17.
10
Technology Insight: small, noncoding RNA molecules as tools to study and treat endocrine diseases.技术洞察:小的非编码RNA分子作为研究和治疗内分泌疾病的工具
Nat Clin Pract Endocrinol Metab. 2007 Dec;3(12):827-34. doi: 10.1038/ncpendmet0674.