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首页> 外文期刊>Journal of neuroendocrinology >Evidence for a gut-brain axis used by glucagon-like peptide-1 to elicit hyperglycaemia in fish.
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Evidence for a gut-brain axis used by glucagon-like peptide-1 to elicit hyperglycaemia in fish.

机译:胰高血糖素样肽1用来引起鱼类高血糖的肠脑轴证据。

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In mammals, glucagon-like peptide-1 (GLP-1) produces changes in glucose and energy homeostasis through a gut-pancreas-brain axis. In fish, the effects of GLP-1 are opposed to those described in other vertebrates, such as stimulation of hyperglycaemia and the lack of an effect of incretin. In the present study conducted in a teleost fish such as the rainbow trout, we present evidence of a gut-brain axis used by GLP-1 to exert its actions on glucose and energy homeostasis. We have assessed the effects of GLP-1 on glucose metabolism in the liver as well as the glucose-sensing potential in the hypothalamus and hindbrain. We confirm that peripheral GLP-1 administration elicits sustained hyperglycaemia, whereas, for the first time in a vertebrate species, we report that central GLP-1 treatment increases plasma glucose levels. We have observed (using capsaicin) that at least part of the action of GLP-1 on glucose homeostasis was mediated by vagal and splanchnic afferents. GLP-1 has a direct effect in parameters involved in glucose sensing in the hindbrain, whereas, in the hypothalamus, changes occurred indirectly through hyperglycaemia. Moreover, in the hindbrain, GLP-1 altered the expression of peptides involved in the control of food intake. We have elaborated a model for the actions of GLP-1 in fish in which this peptide uses a mammalian-like ancestral gut-brain axis to elicit the regulation of glucose homeostasis in different manner than the model described in mammals. Finally, it is worth noting that the hyperglycaemia induced by this peptide and the lack of incretin function could be related to the glucose intolerance observed in carnivorous teleost fish species such as the rainbow trout.
机译:在哺乳动物中,胰高血糖素样肽1(GLP-1)通过肠-胰腺-脑轴产生葡萄糖和能量稳态的变化。在鱼类中,GLP-1的作用与其他脊椎动物中描述的相反,例如刺激高血糖症和缺乏肠降血糖素的作用。在目前对硬骨鱼类(例如虹鳟鱼)进行的研究中,我们提供了GLP-1用以控制其葡萄糖和能量稳态的肠脑轴的证据。我们已经评估了GLP-1对肝脏葡萄糖代谢以及下丘脑和后脑葡萄糖敏感潜能的影响。我们证实,外周给予GLP-1会引起持续的高血糖,而在脊椎动物中,这是首次报道中枢GLP-1的治疗会增加血浆葡萄糖水平。我们已经观察到(使用辣椒素)至少部分GLP-1对葡萄糖稳态的作用是由迷走神经和内脏传入神经介导的。 GLP-1对后脑的葡萄糖传感相关参数有直接影响,而在下丘脑中,变化是通过高血糖症间接发生的。此外,在后脑中,GLP-1改变了控制食物摄入的肽的表达。我们已经为鱼中GLP-1的作用建立了一个模型,其中该肽使用哺乳动物样祖先肠脑轴以与哺乳动物中描述的模型不同的方式引发葡萄糖稳态的调节。最后,值得注意的是,由该肽诱导的高血糖症和肠降血糖素功能的缺乏可能与食肉硬骨鱼类如虹鳟鱼中观察到的葡萄糖耐量异常有关。

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