Hepatic insulin resistance and increased hepatic glucose production in mice lacking Fgf21

被引:46
作者
Camporez, Joao Paulo G. [1 ]
Asrih, Mohamed [3 ]
Zhang, Dongyan [1 ,2 ]
Kahn, Mario [1 ,2 ]
Samuel, Varman T. [1 ]
Jurczak, Michael J. [1 ,2 ]
Jornayvaz, Francois R. [1 ,3 ]
机构
[1] Yale Univ, Dept Internal Med, Sch Med, New Haven, CT 06536 USA
[2] Yale Univ, Howard Hughes Med Inst, Sch Med, New Haven, CT 06536 USA
[3] Univ Lausanne Hosp, Serv Endocrinol Diabet & Metab, Lausanne CHUV, CH-1011 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
FGF21; insulin resistance; NAFLD; energy expenditure; obesity; GROWTH-FACTOR; 21; FATTY LIVER-DISEASE; ENDOPLASMIC-RETICULUM STRESS; KINASE-C-EPSILON; ENERGY-EXPENDITURE; CELLULAR MECHANISMS; LIPID-METABOLISM; OBESITY; SENSITIVITY; ACTIVATION;
D O I
10.1530/JOE-15-0136
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fibroblast growth factor 21 (FGF21) is an important regulator of hepatic glucose and lipid metabolism and represents a potential pharmacological agent for the treatment of type 2 diabetes and obesity. Mice fed a ketogenic diet (KD) develop hepatic insulin resistance in association with high levels of FGF21, suggesting a state of FGF21 resistance. To address the role of FGF21 in hepatic insulin resistance, we assessed insulin action in FGF21 whole-body knock-out (FGF21 KO) male mice and their littermate WT controls fed a KD. Here, we report that FGF21 KO mice have hepatic insulin resistance and increased hepatic glucose production associated with an increase in plasma glucagon levels. FGF21 KO mice are also hypometabolic and display increased fat mass compared with their WT littermates. Taken together, these findings support a major role of FGF21 in regulating energy expenditure and hepatic glucose and lipid metabolism, and its potential role as a candidate in the treatment of diseases associated with insulin resistance.
引用
收藏
页码:207 / 217
页数:11
相关论文
共 63 条
  • [1] Nonalcoholic fatty liver disease
    Brunt, Elizabeth M.
    Wong, Vincent W. -S.
    Nobili, Valerio
    Day, Christopher P.
    Sookoian, Silvia
    Maher, Jacquelyn J.
    Bugianesi, Elisabetta
    Sirlin, Claude B.
    Neuschwander-Tetri, BrentA.
    Rinella, Mary E.
    [J]. NATURE REVIEWS DISEASE PRIMERS, 2015, 1
  • [2] Glucagon increases circulating fibroblast growth factor 21 independently of endogenous insulin levels: a novel mechanism of glucagon-stimulated lipolysis?
    Arafat, A. M.
    Kaczmarek, P.
    Skrzypski, M.
    Pruszynska-Oszmalek, E.
    Kolodziejski, P.
    Szczepankiewicz, D.
    Sassek, M.
    Wojciechowicz, T.
    Wiedenmann, B.
    Pfeiffer, A. F. H.
    Nowak, K. W.
    Strowski, M. Z.
    [J]. DIABETOLOGIA, 2013, 56 (03) : 588 - 597
  • [3] FGF21 attenuates lipolysis in human adipocytes -: A possible link to improved insulin sensitivity
    Arner, Peter
    Pettersson, Amanda
    Mitchell, Pamela J.
    Dunbar, James D.
    Kharitonenkov, Alexei
    Ryden, Mikael
    [J]. FEBS LETTERS, 2008, 582 (12) : 1725 - 1730
  • [4] Metabolic syndrome and nonalcoholic fatty liver disease: Is insulin resistance the link?
    Asrih, Mohamed
    Jornayvaz, Francois R.
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2015, 418 : 55 - 65
  • [5] Ketogenic Diet Impairs FGF21 Signaling and Promotes Differential Inflammatory Responses in the Liver and White Adipose Tissue
    Asrih, Mohamed
    Altirriba, Jordi
    Rohner-Jeanrenaud, Francoise
    Jornayvaz, Francois R.
    [J]. PLOS ONE, 2015, 10 (05):
  • [6] Inflammation as a potential link between nonalcoholic fatty liver disease and insulin resistance
    Asrih, Mohamed
    Jornayvaz, Francois R.
    [J]. JOURNAL OF ENDOCRINOLOGY, 2013, 218 (03) : R25 - R36
  • [7] Standard operating procedures for describing and performing metabolic tests of glucose homeostasis in mice
    Ayala, Julio E.
    Samuel, Varman T.
    Morton, Gregory J.
    Obici, Silvana
    Croniger, Colleen M.
    Shulman, Gerald I.
    Wasserman, David H.
    McGuinness, Owen P.
    [J]. DISEASE MODELS & MECHANISMS, 2010, 3 (9-10) : 525 - 534
  • [8] Badman MK, 2007, CELL METAB, V5, P426, DOI 10.1016/j.cmet.2007.05.002
  • [9] Fibroblast Growth Factor 21-Deficient Mice Demonstrate Impaired Adaptation to Ketosis
    Badman, Michael K.
    Koester, Anja
    Flier, Jeffrey S.
    Kharitonenkov, Alexei
    Maratos-Flier, Eleftheria
    [J]. ENDOCRINOLOGY, 2009, 150 (11) : 4931 - 4940
  • [10] Fibroblast Growth Factor 21 Controls Glycemia via Regulation of Hepatic Glucose Flux and Insulin Sensitivity
    Berglund, Eric D.
    Li, Candice Y.
    Bina, Holly A.
    Lynes, Sara E.
    Michael, M. Dodson
    Shanafelt, Armen B.
    Kharitonenkov, Alexei
    Wasserman, David H.
    [J]. ENDOCRINOLOGY, 2009, 150 (09) : 4084 - 4093