首页> 外文期刊>Hormones and behavior >Ghrelin suppresses cholecystokinin (CCK), peptide YY (PYY) and glucagon-like peptide-1 (GLP-1) in the intestine, and attenuates the anorectic effects of CCK, PYY and GLP-1 in goldfish ( Carassius auratus )
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Ghrelin suppresses cholecystokinin (CCK), peptide YY (PYY) and glucagon-like peptide-1 (GLP-1) in the intestine, and attenuates the anorectic effects of CCK, PYY and GLP-1 in goldfish ( Carassius auratus )

机译:Ghrelin在肠道中抑制胆囊蛋白(CCK),肽YY(PYY)和胰高血糖素样肽-1(GLP-1),并衰减CCK,PYY和GLP-1在金鱼(Carassius auratus)的肛肠效应

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摘要

Abstract Ghrelin is an important gut-derived hormone with an appetite stimulatory role, while most of the intestinal hormones, including cholecystokinin (CCK), peptide YY (PYY) and glucagon-like peptide-1 (GLP-1), are appetite-inhibitors. Whether these important peptides with opposing roles on food intake interact to regulate energy balance in fish is currently unknown. The aim of this study was to characterize the putative crosstalk between ghrelin and CCK, PYY and GLP-1 in goldfish ( Carassius auratus ). We first determined the localization of CCK, PYY and GLP-1 in relation to ghrelin and its main receptor GHS-R1a (growth hormone secretagogue 1a) in the goldfish intestine by immunohistochemistry. Colocalization of ghrelin/GHS-R1a and CCK/PYY/GLP-1 was found primarily in the luminal border of the intestinal mucosa. In an intestinal explant culture, a significant decrease in prepro-cck , prepro-pyy and proglucagon transcript levels was observed after 60 min of incubation with ghrelin, which was abolished by preincubation with the GHS-R1a ghrelin receptor antagonist [D-Lys3]-GHRP-6 (except for proglucagon ). The protein expression of PYY and GLP-1 was also downregulated by ghrelin. Finally, intraperitoneal co-administration of CCK, PYY or GLP-1 with ghrelin results in no modification of food intake in goldfish. Overall, results of the present study show for the first time in fish that ghrelin exerts repressive effects on enteric anorexigens. It is likely that these interactions mediate the stimulatory effects of ghrelin on feeding and metabolism in fish. Highlights ? Ghrelin and GHS-R1a colocalize CCK, PYY and GLP-1 in goldfish intestinal cells. ? Ghrelin suppresses intestinal prepro-cck , prepro-pyy and proglucagon expression in vitro. ? PYY and GLP-1 intestinal levels are downregulated by in vitro ghrelin treatment. ? GHS-R1a is critical for ghrelin-induced downregulation of prepro-cck and prepro-pyy . ? Ghrelin, coadministered with CCK, PYY or GLP-1, is not able to induce goldfish appetite. ]]>
机译:摘要Ghrelin是一种重要的肠道衍生的激素,具有食欲刺激作用,而大多数肠道激素,包括胆囊蛋白(CCK),肽YY(PYY)和胰高血糖素样肽-1(GLP-1)是食欲抑制剂。这些重要肽是否对食物摄入的反对作用相互作用,以调节鱼类的能量平衡目前未知。本研究的目的是在金鱼(Carassius auratus)中的Ghrelin和CCK,Pyy和Glp-1之间的推定串扰。我们首先通过免疫组织化学确定CCK,PYY和GLP-1的定位,PYY和GLP-1与GHRELIN肠道中的GHRELIN及其主要受体GHS-R1A(生长激素分泌素1A)。 Ghrelin / GHS-R1A和CCK / PYY / GLP-1的分致化主要在肠粘膜的腔边界中发现。在肠道培养培养中,在与Ghrelin孵育60分钟后观察到预培养物,Prepro-pey和proglucag转录物水平的显着降低,所述Ghrelin通过预孵育通过预孵育的GHS-R1A Ghrelin受体拮抗剂[D-Lys3] - GHRP-6(Proglucagon除外)。 PYY和GLP-1的蛋白质表达也通过GHRELIN下调。最后,腹膜内的CCK,PYY或GLP-1具有GHRELIN的GLP-1导致金鱼中食物摄入的改性。总体而言,本研究的结果表明在鱼类中的第一次举办了Ghrelin对肠道厌氧的压抑作用。这些相互作用可能会介导Ghrelin对鱼类喂养和代谢的刺激作用。强调 ? Ghrelin和GHS-R1a在金鱼肠道细胞中结冰CCK,PYY和GLP-1。还Ghrelin抑制肠道前CCK,Prepro-Pyy和proglucagon表达在体外。还PYY和GLP-1肠道水平通过体外Ghrelin治疗下调。还GHS-R1A对于Ghrelin诱导的Prepro-CCK和Prepro-Pyy的下调至关重要。还Ghrelin,用CCK,Pyy或GLP-1共同诱导金鱼胃口。 ]]>

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