首页> 美国卫生研究院文献>Metabolites >miR-1/AMPK-Mediated Glucose and Lipid Metabolism under Chronic Hypothermia in the Liver of Freshwater Drum Aplodinotus grunniens
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miR-1/AMPK-Mediated Glucose and Lipid Metabolism under Chronic Hypothermia in the Liver of Freshwater Drum Aplodinotus grunniens

机译:淡水鼓 Aplodinotus grunniens 肝脏慢性低温下 miR-1/AMPK 介导的糖脂代谢

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摘要

Our previous study demonstrated that low temperature could induce hepatic inflammation and suppress the immune and oxidation resistance of freshwater drum. However, the metabolism, especially the glucose and lipid metabolism involved, is poorly studied. To further explore the chronic hypothermia response of freshwater drum, an 8-day hypothermia experiment was conducted at 10 °C to investigate the effect of chronic hypothermia on glucose and lipid metabolism via biochemical and physiological indexes, and metabolic enzyme activities, miRNAs and mRNA-miRNA integrate analysis in the liver. Plasma and hepatic biochemical parameters reveal chronic hypothermia-promoted energy expenditure. Metabolic enzyme levels uncover that glycolysis was enhanced but lipid metabolism was suppressed. Differentially expressed miRNAs induced by hypothermia were mainly involved in glucose and lipid metabolism, programmed cell death, disease, and cancerization. Specifically, KEGG enrichment indicates that AMPK signaling was dysregulated. mRNA-miRNA integrated analysis manifests miR-1 and AMPK, which were actively co-related in the regulatory network. Furthermore, transcriptional expression of key genes demonstrates hypothermia-activated AMPK signaling by miR-1 and subsequently inhibited the downstream glucogenic and glycogenic gene expression and gene expression of fatty acid synthesis. However, glycogenesis was alleviated to the control level while fatty acid synthesis was still suppressed at 8 d. Meanwhile, the gene expressions of glycolysis and fatty acid oxidation were augmented under hypothermia. In conclusion, these results suggest that miR-1/AMPK is an important target for chronic hypothermia control. It provides a theoretical basis for hypothermia resistance on freshwater drum.
机译:我们之前的研究表明,低温可以诱导肝脏炎症并抑制淡水桶的免疫和抗氧化性。然而,对代谢,尤其是所涉及的葡萄糖和脂质代谢的研究很少。为进一步探究淡水桶慢性低温反应,在 10 °C 下进行了为期 8 天的低温实验,通过生化和生理指标以及肝脏代谢酶活性、miRNAs 和 mRNA-miRNA 整合分析来探讨慢性低温对糖脂代谢的影响。血浆和肝脏生化参数显示慢性低体温促进的能量消耗。代谢酶水平发现糖酵解增强,但脂质代谢受到抑制。低温诱导的差异表达 miRNAs 主要参与糖脂代谢、程序性细胞死亡、疾病和癌变。具体而言,KEGG 富集表明 AMPK 信号转导失调。mRNA-miRNA 整合分析显示 miR-1 和 AMPK,它们在调控网络中积极地共相关。此外,关键基因的转录表达表明 miR-1 激活了低温激活的 AMPK 信号传导,随后抑制了下游产糖和糖原基因表达以及脂肪酸合成的基因表达。然而,糖生成减轻至对照水平,而脂肪酸合成在 8 d 时仍受到抑制。同时,在低温下,糖酵解和脂肪酸氧化的基因表达增加。总之,这些结果表明 miR-1/AMPK 是慢性低体温控制的重要靶点。它为淡水桶的低温抵抗提供了理论依据。

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