• 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

AMP激活的蛋白激酶——能量轨道的脂肪调控者。

AMP-activated protein kinase--the fat controller of the energy railroad.

作者信息

Steinberg Gregory R, Macaulay S Lance, Febbraio Mark A, Kemp Bruce E

机构信息

St. Vincent's Institute, 41 Victoria Pd, Fitzroy, 3065 Victoria, Australia.

出版信息

Can J Physiol Pharmacol. 2006 Jul;84(7):655-65. doi: 10.1139/y06-005.

DOI:10.1139/y06-005
PMID:16998529
Abstract

AMP-activated protein kinase plays an important role in the regulation of lipid metabolism in response to metabolic stress and energy demand. It is also under endocrine control. AMPK acts at multiple steps and has a central role controlling fatty acid, triglyceride, and cholesterol synthesis, as well as the oxidation of fatty acids through direct phosphorylation effects and the control of gene transcription. As such, it can be considered to be the fat controller of the energy railroad. It is thought that AMPK may be a major mediator of the health benefits of exercise in mitigating the development of obesity and age-onset diseases.

摘要

AMP激活的蛋白激酶在响应代谢应激和能量需求时对脂质代谢的调节中起重要作用。它也受内分泌控制。AMPK在多个步骤发挥作用,在控制脂肪酸、甘油三酯和胆固醇合成以及通过直接磷酸化作用和基因转录控制来调节脂肪酸氧化方面起着核心作用。因此,它可被视为能量铁路的脂肪控制器。据认为,AMPK可能是运动对减轻肥胖和老年疾病发展有益健康作用的主要介质。

相似文献

1
AMP-activated protein kinase--the fat controller of the energy railroad.AMP激活的蛋白激酶——能量轨道的脂肪调控者。
Can J Physiol Pharmacol. 2006 Jul;84(7):655-65. doi: 10.1139/y06-005.
2
Ethanol consumption impairs regulation of fatty acid metabolism by decreasing the activity of AMP-activated protein kinase in rat liver.乙醇摄入通过降低大鼠肝脏中AMP激活的蛋白激酶活性来损害脂肪酸代谢的调节。
Biochimie. 2008 Mar;90(3):460-6. doi: 10.1016/j.biochi.2007.09.019. Epub 2007 Oct 5.
3
AMP-activated protein kinase and the metabolic syndrome.AMP激活的蛋白激酶与代谢综合征
Biochem Soc Trans. 2005 Apr;33(Pt 2):362-6. doi: 10.1042/BST0330362.
4
Dual regulation of the AMP-activated protein kinase provides a novel mechanism for the control of creatine kinase in skeletal muscle.AMP 激活的蛋白激酶的双重调节为骨骼肌中肌酸激酶的调控提供了一种新机制。
EMBO J. 1998 Mar 16;17(6):1688-99. doi: 10.1093/emboj/17.6.1688.
5
Activation of AMP-activated protein kinase (AMPK) inhibits protein synthesis: a potential strategy to prevent the development of cardiac hypertrophy.AMP激活的蛋白激酶(AMPK)的激活可抑制蛋白质合成:这是一种预防心脏肥大发展的潜在策略。
Can J Physiol Pharmacol. 2005 Jan;83(1):24-8. doi: 10.1139/y04-107.
6
Role of adipokines in the control of energy metabolism: focus on adiponectin.脂肪因子在能量代谢调控中的作用:聚焦脂联素
Curr Opin Pharmacol. 2006 Dec;6(6):580-5. doi: 10.1016/j.coph.2006.08.002. Epub 2006 Sep 14.
7
Synthesis and biological evaluation of benzimidazole derivatives as potent AMP-activated protein kinase activators.作为强效AMP活化蛋白激酶激活剂的苯并咪唑衍生物的合成与生物学评价
Bioorg Med Chem. 2006 Jul 1;14(13):4490-518. doi: 10.1016/j.bmc.2006.02.028. Epub 2006 Mar 2.
8
Regulatory role for the arginine-nitric oxide pathway in metabolism of energy substrates.精氨酸-一氧化氮途径在能量底物代谢中的调节作用。
J Nutr Biochem. 2006 Sep;17(9):571-88. doi: 10.1016/j.jnutbio.2005.12.001. Epub 2006 Jan 9.
9
Chutes and Ladders: the search for protein kinases that act on AMPK.《蛇梯棋:寻找作用于AMPK的蛋白激酶》
Trends Biochem Sci. 2006 Jan;31(1):13-6. doi: 10.1016/j.tibs.2005.11.009. Epub 2005 Dec 13.
10
AMPK and ACC phosphorylation: effect of leptin, muscle fibre type and obesity.AMPK与ACC磷酸化:瘦素、肌纤维类型及肥胖的影响
Mol Cell Endocrinol. 2008 Mar 12;284(1-2):1-10. doi: 10.1016/j.mce.2007.12.013. Epub 2008 Jan 3.

引用本文的文献

1
Association of Genetically Predicted Activity of AMP Deaminase 1 with Clinical and Biochemical Parameters in Diabetic Individuals with Coronary Artery Disease.腺苷酸脱氨酶1基因预测活性与糖尿病合并冠状动脉疾病患者临床及生化参数的关联
Int J Mol Sci. 2025 Aug 21;26(16):8071. doi: 10.3390/ijms26168071.
2
Tissue-specific and spatially dependent metabolic signatures perturbed by injury in skeletally mature male and female mice.骨骼成熟的雄性和雌性小鼠中受损伤干扰的组织特异性和空间依赖性代谢特征。
bioRxiv. 2025 Feb 7:2024.09.30.615873. doi: 10.1101/2024.09.30.615873.
3
Metabolic phenotypes reflect patient sex and injury status: A cross-sectional analysis of human synovial fluid.
代谢表型反映了患者的性别和损伤状况:对人滑膜液的横断面分析。
Osteoarthritis Cartilage. 2024 Sep;32(9):1074-1083. doi: 10.1016/j.joca.2023.09.004. Epub 2023 Sep 15.
4
Serine Racemase mediates subventricular zone neurogenesis via fatty acid metabolism.丝氨酸消旋酶通过脂肪酸代谢介导侧脑室下区神经发生。
Stem Cell Reports. 2023 Jul 11;18(7):1482-1499. doi: 10.1016/j.stemcr.2023.05.015. Epub 2023 Jun 22.
5
Metabolomic Phenotypes Reflect Patient Sex and Injury Status: A Cross-Sectional Analysis of Human Synovial Fluid.代谢组学表型反映患者性别和损伤状态:人体滑液的横断面分析
bioRxiv. 2023 Feb 4:2023.02.03.527040. doi: 10.1101/2023.02.03.527040.
6
Molecular mechanisms of metabolic associated fatty liver disease (MAFLD): functional analysis of lipid metabolism pathways.代谢相关性脂肪性肝病(MAFLD)的分子机制:脂质代谢途径的功能分析。
Clin Sci (Lond). 2022 Sep 30;136(18):1347-1366. doi: 10.1042/CS20220572.
7
Dietary L-arginine supplementation increases the hepatic expression of AMP-activated protein kinase in rats.饮食补充 L-精氨酸可增加大鼠肝组织中 AMP 激活的蛋白激酶的表达。
Amino Acids. 2022 Dec;54(12):1569-1584. doi: 10.1007/s00726-022-03194-w. Epub 2022 Aug 16.
8
Baicalein Prevents Fructose-Induced Hepatic Steatosis in Rats: In the Regulation of Fatty Acid De Novo Synthesis, Fatty Acid Elongation and Fatty Acid Oxidation.黄芩素预防大鼠果糖诱导的肝脂肪变性:在脂肪酸从头合成、脂肪酸延长和脂肪酸氧化的调节方面。
Front Pharmacol. 2022 Jun 30;13:917329. doi: 10.3389/fphar.2022.917329. eCollection 2022.
9
Anti-adipogenic and Pro-lipolytic Effects on 3T3-L1 Preadipocytes by CX-4945, an Inhibitor of Casein Kinase 2.抑制酪蛋白激酶 2 的 CX-4945 对 3T3-L1 前体脂肪细胞的抗脂肪生成和促脂解作用
Int J Mol Sci. 2022 Jun 30;23(13):7274. doi: 10.3390/ijms23137274.
10
Pathological Contribution of Extracellular Vesicles and Their MicroRNAs to Progression of Chronic Liver Disease.细胞外囊泡及其微小RNA对慢性肝病进展的病理作用
Biology (Basel). 2022 Apr 21;11(5):637. doi: 10.3390/biology11050637.