Institute of Cellular and Organismic Biology, Academia Sinica, Nankang, Taipei, Taiwan, ROC.
Comp Biochem Physiol A Mol Integr Physiol. 2010 Jun;156(2):190-200. doi: 10.1016/j.cbpa.2010.01.019. Epub 2010 Feb 4.
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 zghrl 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 zgcgb2; 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.
碳水化合物-糖原代谢 (CGM) 对中枢神经系统 (CNS) 的紧急能量供应至关重要。已知胰腺中的生长激素释放肽 (GHRL) 可显著调节 CGM 中的主要参与者胰岛素 (INS)。然而,其对胰外 INS 合成的调节作用尚不清楚。在这项研究中,我们使用成年斑马鱼来阐明参与大脑 CGM 的主要基因中斑马鱼 GHRL (zGHRL) 的表达和作用。结果表明,根据 RT-PCR 和原位杂交,斑马鱼大脑表达 zghrl 及其受体,生长激素释放肽受体 (GHS-R:zghs-r1a 和 zghs-r2a)。蛋白定位与 mRNA 空间表达进一步证实了 zGHRL 在大脑中的存在。在体内研究中,使用脑模板通过定量实时 PCR (qPCR) 分析,注射合成肽金鱼 GHRL-12 (gGHRL) 后,观察到 zghs-r1a 和 zghs-r2a 合成的显著增加。胰岛素 (zinsa; zins-r1 和 zins-r2) 的配体-受体合成显著减少,而胰高血糖素 (GCG) (zgcgb1 和 zgcgb2; zgcg-r1 和 zgcg-r2) 则表现出显著的短暂增加。在 CGM 中,随后的过程表明存在紧急的葡萄糖感应反应,这将平衡糖原降解和能量储存。综上所述,这些发现表明 GHRL 通过在 CNS 中介导其对 GHS-R 的作用来调节 INS 合成,并部分参与 CGM。