Ghrelin affects carbohydrate-glycogen metabolism via insulin inhibition and glucagon stimulation in the zebrafish (Danio rerio) brain

被引:52
作者
Cruz, Shelly A. [1 ,2 ]
Tseng, Yung-Che [1 ]
Kaiya, Hiroyuki [3 ]
Hwang, Pung Pung [1 ,2 ]
机构
[1] Acad Sinica, Inst Cellular & Organism Biol, Taipei 11521, Taiwan
[2] Natl Taiwan Univ, Coll Life Sci, Inst Fisheries Sci, Taipei 10764, Taiwan
[3] Natl Cardiovasc Ctr, Res Inst, Dept Biochem, Osaka, Japan
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY | 2010年 / 156卷 / 02期
关键词
Brain; Ghrelin; Glucagon; Glycogen growth hormone secretagogue receptor; Insulin; RECEPTOR (GHS-R)-LIKE RECEPTOR; HORMONE SECRETAGOGUE RECEPTOR; GROWTH-HORMONE; CDNA CLONING; FUNCTIONAL-CHARACTERIZATION; GENOMIC ORGANIZATION; PANCREATIC-ISLETS; GENE-EXPRESSION; PITUITARY-CELLS; NEUROPEPTIDE-Y;
D O I
10.1016/j.cbpa.2010.01.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Carbohydrate-glycogen metabolism (CGM) is critical for emergency energy supplies in the central nervous system (CNS). Ghrelin (GHRL) in pancreas is known to significantly regulate a dominant player in CGM, insulin (INS). However, its regulatory effect on extrapancreatic INS synthesis is yet unknown. In this study, we used adult zebrafish to elucidate the expression and role of zebrafish GHRL (zGHRL) in genes primarily involved in the brain's CGM. Results showed that zebrafish brain expressed zghr1 and its receptor, growth hormone secretagogue-receptor (GHS-R: zghs-r1a and zghs-r2a), according to RT-PCR and in situ hybridization. Protein localization coupled with mRNA spatial expression further verified zGHRL's presence in the brain. For the in vivo study, significant increases in zghs-r1a and zghs-r2a synthesis were observed after injection of synthetic peptide goldfish GHRL-12 (gGHRL) using brain templates analyzed by quantitative real-time PCR (qPCR). Ligand-receptor synthesis of INS (zinsa; zins-r1 and zins-r2) significantly decreased, while glucagon (GCG) (zgcgb1 and zgcg62; zgcg-r1 and zgcg-r2) exhibited a significant transient increase. In CGM, subsequent processes indicate urgent glucose-sensing response that will balance glycogen degradation and energy storage. Taken together, these findings suggest that GHRL regulates INS synthesis by mediating its action on GHS-R in the CNS and partly involved in CGM. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:190 / 200
页数:11
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