首页> 外文期刊>Canadian Journal of Physiology and Pharmacology >Regulation of liver glucokinase activity in rats with fructose-induced insulin resistance and impaired glucose and lipid metabolism.
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Regulation of liver glucokinase activity in rats with fructose-induced insulin resistance and impaired glucose and lipid metabolism.

机译:对果糖诱导的胰岛素抵抗和葡萄糖和脂质代谢受损的大鼠肝脏葡萄糖激酶活性的调节。

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摘要

We evaluated the relative role of different regulatory mechanisms, particularly 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase (PFK2/FBPase-2), in liver glucokinase (GK) activity in intact animals with fructose-induced insulin resistance and impaired glucose and lipid metabolism. We measured blood glucose, triglyceride and insulin concentration, glucose tolerance, liver triglyceride content, GK activity, and GK and PFK2 protein and gene expression in fructose-rich diet (FRD) and control rats. After 3 weeks, FRD rats had significantly higher blood glucose, insulin and triglyceride levels, and liver triglyceride content, insulin resistance, and impaired glucose tolerance. FRD rats also had significantly higher GK activity in the cytosolic fraction (18.3 +/- 0.35 vs. 11.27 +/- 0.34 mU/mg protein). Differences in GK protein concentration (116% and 100%) were not significant, suggesting a potentially impaired GK translocation in FRD rats. Although GK transcription level was similar, PFK2 gene expression and protein concentration were 4- and 5-fold higher in the cytosolic fraction of FRD animals. PFK2 immunological blockage significantly decreased GK activity in control and FRD rats; in the latter, this blockage decreased GK activity to control levels. Results suggest that increased liver GK activity might participate in the adaptative response to fructose overload to maintain glucose/triglyceride homeostasis in intact animals. Under these conditions, PFK2 increase would be the main enhancer of GK activity.
机译:我们评估了不同调节机制的相对作用,特别是6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶(PFK2 / FBPase-2)在具有果糖诱导的胰岛素抵抗的完整动物的肝脏葡萄糖激酶(GK)活性中的相对作用。并损害糖脂代谢。我们测量了富果糖饮食(FRD)和对照组大鼠的血糖,甘油三酸酯和胰岛素浓度,葡萄糖耐量,肝脏甘油三酸酯含量,GK活性以及GK和PFK2蛋白和基因表达。 3周后,FRD大鼠的血糖,胰岛素和甘油三酸酯水平明显升高,肝脏甘油三酸酯含量,胰岛素抵抗和葡萄糖耐量降低。 FRD大鼠在胞浆中的GK活性也明显更高(18.3 +/- 0.35 vs. 11.27 +/- 0.34 mU / mg蛋白)。 GK蛋白浓度(116%和100%)的差异不显着,表明FRD大鼠中GK易位可能受损。尽管GK转录水平相似,但FRD动物的细胞质分数中PFK2基因表达和蛋白质浓度分别高4和5倍。 PFK2免疫阻断明显降低了对照组和FRD大鼠的GK活性;在后者中,这种阻断作用将GK活性降低至控制水平。结果表明,增加的肝脏GK活性可能参与了对果糖超负荷的适应性反应,从而维持了完整动物体内的葡萄糖/甘油三酸酯稳态。在这些条件下,PFK2的增加将是GK活性的主要增强剂。

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