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首页> 外文期刊>Comparative biochemistry and physiology, Part B. Biochemistry & molecular biology >Changes in expression of hepatic genes involved in energy metabolism during hibernation in captive, adult, female Japanese black bears (Ursus thibetanus japonicus)
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Changes in expression of hepatic genes involved in energy metabolism during hibernation in captive, adult, female Japanese black bears (Ursus thibetanus japonicus)

机译:肝基因表达的变化能量代谢在人工冬眠期间,成年人,女性日本黑熊(熊属

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摘要

Hibernating bears survive up to 6. months without feeding by utilizing stored body fat as fuel. To investigate how bears maintain energy homeostasis during hibernation, we analyzed changes in mRNA expression of hepatic genes involved in energy metabolism throughout the hibernation period in captive, adult, female Japanese black bears (Ursus thibetanus japonicus). Real-time PCR analysis revealed down-regulation of glycolysis- (e.g., glucokinase), amino acid catabolism- (e.g., alanine aminotransferase) and de novo lipogenesis-related genes (e.g., acetyl-CoA carboxylase 1), and up-regulation of gluconeogensis- (e.g., pyruvate carboxylase), β-oxidation- (i.e., uncoupling protein 2) and ketogenesis-related genes (i.e., 3-hydroxy-3-methylglutary-CoA synthase 2), during hibernation, compared to the active period (June). In addition, we found that glycolysis-related genes (i.e., glucokinase and pyruvate kinase) were more suppressed in the early phase of hibernation (January) compared to the late phase (March). One week after the commencement of feeding in April, expression levels of most genes returned to levels comparable to those seen in June, but β-oxidation-related genes were still up-regulated during this period. These results suggest that the modulation of gene expression is not static, but changes throughout the hibernation period. The transcriptional modulation during hibernation represents a unique physiological adaptation to prolonged fasting in bears.
机译:冬眠熊生存6。利用体内储存的脂肪作为燃料。研究熊保持体内平衡能量冬眠期间,我们分析了信使rna的变化肝基因表达参与能量在整个冬眠时期新陈代谢日本黑熊俘虏,成年人,女性分析发现糖酵解,下调(例如,葡糖激酶),氨基酸分解代谢(例如,丙氨酸转氨酶)和新创lipogenesis-related基因(如乙酰辅酶a羧化酶1),和老年病gluconeogensis(如丙酮酸羧化酶),β氧化-(即解偶联蛋白2)ketogenesis-related基因(即3-hydroxy-3-methylglutary-CoA合成酶2),期间冬眠,而活跃的时期(6月)。(例如,葡糖激酶和glycolysis-related基因丙酮酸激酶)更多的镇压冬眠的早期阶段(1月)相比后期阶段(3月)。4月份开始喂养,表达式大多数基因水平回到水平6月媲美,但是β-oxidation-related仍然上调的基因在这段时间。基因表达不是静态的调制,但在冬眠期变化。转录调制在冬眠代表一个独特的生理适应长期禁食熊。

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