Role of the liver in the control of carbohydrate and lipid homeostasis

被引:340
作者
Postic, C [1 ]
Dentin, R [1 ]
Girard, J [1 ]
机构
[1] Univ Paris 05, CNRS, INSERM, UMR 8104,U567,Inst Cochin,Dept Endocrinol, F-75014 Paris, France
关键词
liver; glucose metabolism; lipid synthesis; glucose and insulin signaling; transgenic and knockout; mouse models; gene regulation;
D O I
10.1016/S1262-3636(07)70133-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The liver plays a unique role in controlling carbohydrate metabolism by maintaining glucose concentrations in a normal range over both short and long periods of times. In type 2 diabetes, alterations in hepatic glucose metabolism are observed, i.e. increased post-absorptive glucose production and impaired suppression of glucose production together with diminished glucose uptake following carbohydrate ingestion. The simultaneous overproduction of glucose and fatty acids in liver further stimulates the secretion of insulin by the pancreatic beta cells, and elicits further peripheral insulin resistance thereby establishing a vicious circle. The present review will focus on some of the genetically-altered mouse models that have helped identify enzymes or transcription factors that are essential for maintaining either glucose or lipid homeostasis in liver. Among these mouse models, we will discuss transgenic mice overexpressing key gluconeogenic enzymes (PEPCK, G6Pase) or transcription factors (Foxo1, Pgc1-alpha) that control de novo glucose synthesis. In addition, since the possibility of controlling hepatic glucose utilization as a treatment of type 2 diabetes has been explored we will review some of the strategies proved to be valuable for improving the hyperglycemic phenotype.
引用
收藏
页码:398 / 408
页数:11
相关论文
共 91 条
[31]   SREBPs suppress IRS-2-mediated insulin signalling in the liver [J].
Ide, T ;
Shimano, H ;
Yahagi, N ;
Matsuzaka, T ;
Nakakuki, M ;
Yamamoto, T ;
Nakagawa, Y ;
Takahashi, A ;
Suzuki, H ;
Sone, H ;
Toyoshima, H ;
Fukamizu, A ;
Yamada, N .
NATURE CELL BIOLOGY, 2004, 6 (04) :351-357
[32]   Deficiency of carbohydrate response element-binding protein (ChREBP) reduces lipogenesis as well as glycolysis [J].
Iizuka, K ;
Bruick, RK ;
Liang, G ;
Horton, JD ;
Uyeda, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (19) :7281-7286
[33]   Role of STAT-3 in regulation of hepatic gluconeogenic genes and carbohydrate metabolism in vivo [J].
Inoue, H ;
Ogawa, W ;
Ozaki, M ;
Haga, S ;
Matsumoto, M ;
Furukawa, K ;
Hashimoto, N ;
Kido, Y ;
Mori, T ;
Sakaue, H ;
Teshigawara, K ;
Jin, SY ;
Iguchi, H ;
Hiramatsu, R ;
LeRoith, D ;
Takeda, K ;
Akira, S ;
Kasuga, M .
NATURE MEDICINE, 2004, 10 (02) :168-174
[34]  
IYNEDJIAN PB, 1989, J BIOL CHEM, V264, P21824
[35]   Xylulose 5-phosphate mediates glucose-induced lipogenesis by xylulose 5-phosphate-activated protein phosphatase in rat liver [J].
Kabashima, T ;
Kawaguchi, T ;
Wadzinski, BE ;
Uyeda, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (09) :5107-5112
[36]   Glucose and cAMP regulate the L-type pyruvate kinase gene by phosphorylation/dephosphorylation of the carbohydrate response element binding protein [J].
Kawaguchi, T ;
Takenoshita, M ;
Kabashima, T ;
Uyeda, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13710-13715
[37]   Glucose and insulin function through two distinct transcription factors to stimulate expression of lipogenic enzyme genes in liver [J].
Koo, SH ;
Dutcher, AK ;
Towle, HC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (12) :9437-9445
[38]   Direct control of the Forkhead transcription factor AFX by protein kinase B [J].
Kops, GJPL ;
de Ruiter, ND ;
De Vries-Smits, AMM ;
Powell, DR ;
Bos, JL ;
Burgering, BMT .
NATURE, 1999, 398 (6728) :630-634
[39]   New insights into the role and mechanism of glycogen synthase activation by insulin [J].
Lawrence, JC ;
Roach, PJ .
DIABETES, 1997, 46 (04) :541-547
[40]  
LEI KJ, 1995, AM J HUM GENET, V57, P766