Plasma FGF21 concentrations, adipose fibroblast growth factor receptor-1 and β-klotho expression decrease with fasting in northern elephant seals

被引:6
|
作者
Suzuki, Miwa [1 ,2 ]
Lee, Andrew Y. [1 ]
Vazquez-Medina, Jose Pablo [1 ]
Viscarra, Jose A. [1 ]
Crocker, Daniel E. [3 ]
Ortiz, Rudy M. [1 ]
机构
[1] Univ Calif Merced, Dept Mol & Cellular Biol, Merced, CA 95343 USA
[2] Nihon Univ, Coll Bioresource Sci, Fujisawa, Kanagawa 2520880, Japan
[3] Sonoma State Univ, Dept Biol, Rohnert Pk, CA 94928 USA
基金
日本学术振兴会;
关键词
Fibroblast growth factor 21; Fasting; Food deprivation; Elephant seal; INSULIN SENSITIVITY; PPAR-ALPHA; TNF-ALPHA; METABOLISM; FIBROBLAST-GROWTH-FACTOR-21; GAMMA; ACTIVATION;
D O I
10.1016/j.ygcen.2015.03.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fibroblast growth factor (FGF)-21 is secreted from the liver, pancreas, and adipose in response to prolonged fasting/starvation to facilitate lipid and glucose metabolism. Northern elephant seals naturally fast for several months, maintaining a relatively elevated metabolic rate to satisfy their energetic requirements. Thus, to better understand the impact of prolonged food deprivation on FGF21-associated changes, we analyzed the expression of FGF21, FGF receptor-1 (FGFR1), beta-klotho (KLB; a co-activator of FGFR) in adipose, and plasma FGF21, glucose and 3-hydroxybutyrate in fasted elephant seal pups. Expression of FGFR1 and KLB mRNA decreased 98% and 43%, respectively, with fasting duration. While the 80% decrease in mean adipose FGF21 mRNA expression with fasting did not reach statistical significance, it paralleled the 39% decrease in plasma FGF21 concentrations suggesting that FGF21 is suppressed with fasting in elephant seals. Data demonstrate an atypical response of FGF21 to prolonged fasting in a mammal suggesting that FGF21-mediated mechanisms have evolved differentially in elephant seals. Furthermore, the typical fasting-induced, FGF21-mediated actions such as the inhibition of lipolysis in adipose may not be required in elephant seals as part of a naturally adapted mechanism to support their unique metabolic demands during prolonged fasting. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:86 / 89
页数:4
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