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首页> 外文期刊>The Journal of Nutritional Biochemistry >Biotin increases glucokinase expression via soluble guanylate cyclase/protein kinase G, adenosine triphosphate production and autocrine action of insulin in pancreatic rat islets
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Biotin increases glucokinase expression via soluble guanylate cyclase/protein kinase G, adenosine triphosphate production and autocrine action of insulin in pancreatic rat islets

机译:生物素通过可溶性鸟苷酸环化酶/蛋白激酶G,三磷酸腺苷的产生和胰岛素在胰腺大鼠胰岛中的自分泌作用来提高葡萄糖激酶的表达

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摘要

Besides its role as a carboxylase prosthetic group, biotin has important effects on gene expression. However, the molecular mechanisms through which biotin exerts these effects are largely unknown. We previously found that biotin increases pancreatic glucokinase expression. We have now explored the mechanisms underlying this effect. Pancreatic islets from Wistar rats were treated with biotin, in the presence or absence of different types of inhibitors. Glucokinase mRNA and 18s rRNA abundance were determined by real-time PCR. Adenosine triphosphate (ATP) content was analyzed by fluorometry. Biotin treatment increased glucokinase mRNA abundance approximately onefold after 2 h; the effect was sustained up to 24 h. Inhibition of soluble guanylate cyclase or protein kinase G (PKG) signalling suppressed biotin-induced glucokinase expression. The cascade of events downstream of PKG in biotin-mediated gene transcription is not known. We found that inhibition of insulin secretion with diazoxide or nifedipine prevented biotin-stimulated glucokinase mRNA increase. Biotin treatment increased islet ATP content (control: 4.68 +/- 0.28; biotin treated: 6.62 +/- 0.26 pmol/islet) at 30 min. Inhibition of PKG activity suppressed the effects of biotin on ATP content. Insulin antibodies or inhibitors of phosphoinositol-3-kinase/Akt insulin signalling pathway prevented biotin-induced glucokinase expression. The nucleotide 8-Br-cGMP mimicked the biotin effects. We propose that the induction of pancreatic glucokinase mRNA by biotin involves guanylate cyclase and PKG activation, which leads to an increase in ATP content. This induces insulin secretion via ATP-sensitive potassium channels. Autocrine insulin, in turn, activates phosphoinositol-3-kinase/Akt signalling. Our results offer new insights into the pathways that participate in biotin-mediated gene expression
机译:除了其作为羧化酶辅基的作用外,生物素还对基因表达有重要影响。然而,生物素通过其发挥这些作用的分子机制尚不清楚。我们先前发现生物素可增加胰腺葡萄糖激酶的表达。现在,我们已经探索了这种作用的潜在机制。在存在或不存在不同类型抑制剂的情况下,用生物素处理来自Wistar大鼠的胰岛。通过实时PCR测定葡萄糖激酶mRNA和18s rRNA的丰度。通过荧光法分析三磷酸腺苷(ATP)的含量。生物素处理在2小时后使葡萄糖激酶mRNA的丰度提高了约一倍。效果持续24小时。可溶性鸟苷酸环化酶或蛋白激酶G(PKG)信号的抑制抑制了生物素诱导的葡萄糖激酶的表达。在生物素介导的基因转录中PKG下游事件的级联是未知的。我们发现用二氮嗪或硝苯地平抑制胰岛素分泌可防止生物素刺激的葡萄糖激酶mRNA的增加。生物素处理在30分钟时增加了胰岛ATP含量(对照:4.68 +/- 0.28;生物素处理:6.62 +/- 0.26 pmol /岛)。 PKG活性的抑制抑制了生物素对ATP含量的影响。胰岛素抗体或磷酸肌醇-3-激酶/ Akt胰岛素信号通路的抑制剂阻止了生物素诱导的葡萄糖激酶表达。核苷酸8-Br-cGMP模仿了生物素的作用。我们建议生物素诱导胰腺葡萄糖激酶mRNA涉及鸟苷酸环化酶和PKG激活,从而导致ATP含量增加。这会通过ATP敏感性钾通道诱导胰岛素分泌。反过来,自分泌胰岛素会激活磷酸肌醇3激酶/ Akt信号传导。我们的结果为参与生物素介导的基因表达的途径提供了新见解

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