Insulin regulation of gluconeogenesis

被引:416
作者
Hatting, Maximilian [1 ,2 ]
Tavares, Clint D. J. [1 ,2 ]
Sharabi, Kfir [1 ,2 ]
Rines, Amy K. [1 ,2 ]
Puigserver, Pere [1 ,2 ]
机构
[1] Dana Farber Canc Inst, Dept Canc Biol, 450 Brookline Av,CLSB 11144, Boston, MA 02215 USA
[2] Harvard Med Sch, Dept Cell Biol, Boston, MA USA
关键词
glycogenolysis; glucose; regulation; gluconeogenesis; insulin; ACTIVATED PROTEIN-KINASE; HEPATIC GLUCOSE-PRODUCTION; TRANSCRIPTION FACTOR FOXO1; ELEMENT-BINDING PROTEIN; FATTY-ACID OXIDATION; GENOME-WIDE ANALYSIS; PHOSPHOENOLPYRUVATE CARBOXYKINASE; GENE-EXPRESSION; PPAR-GAMMA; RECEPTOR SUBSTRATE-1;
D O I
10.1111/nyas.13435
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The coordinated regulation between cellular glucose uptake and endogenous glucose production is indispensable for the maintenance of constant blood glucose concentrations. The liver contributes significantly to this process by altering the levels of hepatic glucose release, through controlling the processes of de novo glucose production (gluconeogenesis) and glycogen breakdown (glycogenolysis). Various nutritional and hormonal stimuli signal to alter hepatic gluconeogenic flux, and suppression of this metabolic pathway during the postprandial state can, to a significant extent, be attributed to insulin. Here, we review some of the molecular mechanisms through which insulin modulates hepatic gluconeogenesis, thus controlling glucose production by the liver to ultimately maintain normoglycemia. Various signaling pathways governed by insulin converge at the level of transcriptional regulation of the key hepatic gluconeogenic genes PCK1 and G6PC, highlighting this as one of the focal mechanisms through which gluconeogenesis is modulated. In individuals with compromised insulin signaling, such as insulin resistance in type 2 diabetes, insulin fails to suppress hepatic gluconeogenesis, even in the fed state; hence, an insight into these insulin-moderated pathways is critical for therapeutic purposes.
引用
收藏
页码:21 / 35
页数:15
相关论文
共 135 条
[1]   Assessment of the roles of mitogen-activated protein kinase, phosphatidylinositol 3-kinase, protein kinase B, and protein kinase C in insulin inhibition of cAMP-induced phosphoenolpyruvate carboxykinase gene transcription [J].
Agati, JM ;
Yeagley, D ;
Quinn, PG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (30) :18751-18759
[2]   Insulin Directly Regulates Steroidogenesis via Induction of the Orphan Nuclear Receptor DAX-1 in Testicular Leydig Cells [J].
Ahn, Seung Won ;
Gang, Gil-Tae ;
Kim, Yong Deuk ;
Ahn, Ryun-Sup ;
Harris, Robert A. ;
Lee, Chul-Ho ;
Choi, Hueng-Sik .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (22) :15937-15946
[3]   CREB and the CRTC co-activators: sensors for hormonal and metabolic signals [J].
Altarejos, Judith Y. ;
Montminy, Marc .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2011, 12 (03) :141-151
[4]   Inhibitors of CLK Protein Kinases Suppress Cell Growth and Induce Apoptosis by Modulating Pre-mRNA Splicing [J].
Araki, Shinsuke ;
Dairiki, Ryo ;
Nakayama, Yusuke ;
Murai, Aiko ;
Miyashita, Risa ;
Iwatani, Misa ;
Nomura, Toshiyuki ;
Nakanishi, Osamu .
PLOS ONE, 2015, 10 (01)
[5]   Mitogen-activated protein kinases, Erk and p38, phosphorylate and regulate Foxo1 [J].
Asada, Sachie ;
Daitoku, Hiroaki ;
Matsuzaki, Hitomi ;
Saito, Tomoko ;
Sudo, Tatsuhiko ;
Mukai, Hidehito ;
Iwashita, Shintaro ;
Kako, Koichiro ;
Kishi, Tsutomu ;
Kasuya, Yoshitoshi ;
Fukamizu, Akiyoshi .
CELLULAR SIGNALLING, 2007, 19 (03) :519-527
[6]   Conservation of an insulin response unit between mouse and human glucose-6-phosphatase catalytic subunit gene promoters - Transcription factor FKHR binds the insulin response sequence [J].
Ayala, JE ;
Streeper, RS ;
Desgrosellier, JS ;
Durham, SK ;
Suwanichkul, A ;
Svitek, CA ;
Goldman, JK ;
Barr, FG ;
Powell, DR ;
O'Brien, RM .
DIABETES, 1999, 48 (09) :1885-1889
[7]   Novel concepts in insulin regulation of hepatic gluconeogenesis [J].
Barthel, A ;
Schmoll, D .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2003, 285 (04) :E685-E692
[8]   Cyclin D1 Represses Gluconeogenesis via Inhibition of the Transcriptional Coactivator PGC1α [J].
Bhalla, Kavita ;
Liu, Wan-Ju ;
Thompson, Keyata ;
Anders, Lars ;
Devarakonda, Srikripa ;
Dewi, Ruby ;
Buckley, Stephanie ;
Hwang, Bor-Jang ;
Polster, Brian ;
Dorsey, Susan G. ;
Sun, Yezhou ;
Sicinski, Piotr ;
Girnun, Geoffrey D. .
DIABETES, 2014, 63 (10) :3266-3278
[9]   Hepatic insulin resistance is sufficient to produce dyslipidemia and susceptibility to atherosclerosis [J].
Biddinger, Sudha B. ;
Hernandez-Ono, Antonio ;
Rask-Madsen, Christian ;
Haas, Joel T. ;
Aleman, Jose O. ;
Suzuki, Ryo ;
Scapa, Erez F. ;
Agarwal, Chhavi ;
Carey, Martin C. ;
Stephanopoulos, Gregory ;
Cohen, David E. ;
King, George L. ;
Ginsberg, Henry N. ;
Kahn, C. Ronald .
CELL METABOLISM, 2008, 7 (02) :125-134
[10]   Insulin, but not contraction, activates Akt/PKB in isolated rat skeletal muscle [J].
Brozinick, JT ;
Birnbaum, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (24) :14679-14682