Suppr超能文献

肝脏中AMP活化蛋白激酶的激活:一种治疗代谢性肝脏疾病的新策略。

Activation of AMP-activated protein kinase in the liver: a new strategy for the management of metabolic hepatic disorders.

作者信息

Viollet Benoit, Foretz Marc, Guigas Bruno, Horman Sandrine, Dentin Renaud, Bertrand Luc, Hue Louis, Andreelli Fabrizio

机构信息

Institut Cochin, INSERM U567, Department of Endocrinology, Metabolism and Cancer, 24 rue du Faubourg Saint Jacques, Paris 75014, France.

出版信息

J Physiol. 2006 Jul 1;574(Pt 1):41-53. doi: 10.1113/jphysiol.2006.108506. Epub 2006 Apr 27.

Abstract

It is now becoming evident that the liver has an important role in the control of whole body metabolism of energy nutrients. In this review, we focus on recent findings showing that AMP-activated protein kinase (AMPK) plays a major role in the control of hepatic metabolism. AMPK integrates nutritional and hormonal signals to promote energy balance by switching on catabolic pathways and switching off ATP-consuming pathways, both by short-term effects on phosphorylation of regulatory proteins and by long-term effects on gene expression. Activation of AMPK in the liver leads to the stimulation of fatty acid oxidation and inhibition of lipogenesis, glucose production and protein synthesis. Medical interest in the AMPK system has recently increased with the demonstration that AMPK could mediate some of the effects of the fat cell-derived adiponectin and the antidiabetic drugs metformin and thiazolidinediones. These findings reinforce the idea that pharmacological activation of AMPK may provide, through signalling and metabolic and gene expression effects, a new strategy for the management of metabolic hepatic disorders linked to type 2 diabetes and obesity.

摘要

目前越来越明显的是,肝脏在控制全身能量营养物质代谢方面发挥着重要作用。在本综述中,我们聚焦于近期的研究发现,即AMP激活的蛋白激酶(AMPK)在肝脏代谢控制中起主要作用。AMPK整合营养和激素信号,通过开启分解代谢途径和关闭ATP消耗途径来促进能量平衡,这既通过对调节蛋白磷酸化的短期作用,也通过对基因表达的长期作用来实现。肝脏中AMPK的激活会导致脂肪酸氧化的刺激以及脂肪生成、葡萄糖生成和蛋白质合成的抑制。最近,随着AMPK可介导脂肪细胞衍生的脂联素以及抗糖尿病药物二甲双胍和噻唑烷二酮的某些作用得到证实,医学界对AMPK系统的兴趣有所增加。这些发现强化了这样一种观点,即AMPK的药理学激活可能通过信号传导、代谢和基因表达效应,为管理与2型糖尿病和肥胖相关的代谢性肝脏疾病提供一种新策略。

相似文献

1
Activation of AMP-activated protein kinase in the liver: a new strategy for the management of metabolic hepatic disorders.
J Physiol. 2006 Jul 1;574(Pt 1):41-53. doi: 10.1113/jphysiol.2006.108506. Epub 2006 Apr 27.
3
Targeting AMP-activated protein kinase as a novel therapeutic approach for the treatment of metabolic disorders.
Diabetes Metab. 2007 Dec;33(6):395-402. doi: 10.1016/j.diabet.2007.10.004. Epub 2007 Nov 7.
4
AMP-activated protein kinase in metabolic control and insulin signaling.
Circ Res. 2007 Feb 16;100(3):328-41. doi: 10.1161/01.RES.0000256090.42690.05.
5
AMP-activated protein kinase and type 2 diabetes.
Curr Med Chem. 2006;13(5):583-9. doi: 10.2174/092986706776055724.
6
Role of AMP-activated protein kinase in mechanism of metformin action.
J Clin Invest. 2001 Oct;108(8):1167-74. doi: 10.1172/JCI13505.
7
Acetic acid activates hepatic AMPK and reduces hyperglycemia in diabetic KK-A(y) mice.
Biochem Biophys Res Commun. 2006 Jun 2;344(2):597-604. doi: 10.1016/j.bbrc.2006.03.176. Epub 2006 Apr 5.
8
AMP activated protein kinase: a next generation target for total metabolic control.
Expert Opin Ther Targets. 2008 Jan;12(1):91-100. doi: 10.1517/14728222.12.1.91.
9
Role of AMP-activated protein kinase in the metabolic syndrome and in heart disease.
FEBS Lett. 2008 Jan 9;582(1):81-9. doi: 10.1016/j.febslet.2007.11.018. Epub 2007 Nov 20.

引用本文的文献

5
Bioactive small compounds effectively inhibit ChREBP overexpression to treat NAFLD and T2DM: A computational drug development approach.
Heliyon. 2025 Feb 10;11(4):e42477. doi: 10.1016/j.heliyon.2025.e42477. eCollection 2025 Feb 28.
6
Dysregulated hepatic alcohol metabolism: a key factor involved in the pathogenesis of alcohol-associated liver disease.
Am J Physiol Gastrointest Liver Physiol. 2025 Mar 1;328(3):G289-G308. doi: 10.1152/ajpgi.00394.2024. Epub 2025 Feb 5.
7
Nidogen 2 Overexpression Promotes Hepatosteatosis and Atherosclerosis.
Int J Mol Sci. 2024 Nov 28;25(23):12782. doi: 10.3390/ijms252312782.
8
Loss of protects against MASLD alone or with alcohol intake by preserving lipid homeostasis.
JHEP Rep. 2024 Oct 5;7(1):101230. doi: 10.1016/j.jhepr.2024.101230. eCollection 2025 Jan.
9
Fine-tuning AMPK in physiology and disease using point-mutant mouse models.
Dis Model Mech. 2024 Aug 1;17(8). doi: 10.1242/dmm.050798. Epub 2024 Aug 13.
10
Efficacy and Safety of Bempedoic Acid in Patients With Hyperlipidemia and Non-alcoholic Fatty Liver Disease.
J Community Hosp Intern Med Perspect. 2024 Mar 4;14(2):40-48. doi: 10.55729/2000-9666.1313. eCollection 2024.

本文引用的文献

2
Hypoxia-induced energy stress regulates mRNA translation and cell growth.
Mol Cell. 2006 Feb 17;21(4):521-31. doi: 10.1016/j.molcel.2006.01.010.
5
The kinase LKB1 mediates glucose homeostasis in liver and therapeutic effects of metformin.
Science. 2005 Dec 9;310(5754):1642-6. doi: 10.1126/science.1120781. Epub 2005 Nov 24.
6
Growing roles for the mTOR pathway.
Curr Opin Cell Biol. 2005 Dec;17(6):596-603. doi: 10.1016/j.ceb.2005.09.009. Epub 2005 Oct 13.
8
The CREB coactivator TORC2 is a key regulator of fasting glucose metabolism.
Nature. 2005 Oct 20;437(7062):1109-11. doi: 10.1038/nature03967. Epub 2005 Sep 7.
9
Activating AMP-activated protein kinase without AMP.
Mol Cell. 2005 Aug 5;19(3):289-90. doi: 10.1016/j.molcel.2005.07.012.
10
AMP-activated protein kinase and coordination of hepatic fatty acid metabolism of starved/carbohydrate-refed rats.
Am J Physiol Endocrinol Metab. 2005 Nov;289(5):E794-800. doi: 10.1152/ajpendo.00144.2005. Epub 2005 Jun 14.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验