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Opposing Activity Changes in AMP Deaminase and AMP-Activated Protein Kinase in the Hibernating Ground Squirrel

机译:冬眠地松鼠中AMP脱氨酶和AMP激活的蛋白激酶的相反活性变化

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摘要

Hibernating animals develop fatty liver when active in summertime and undergo a switch to a fat oxidation state in the winter. We hypothesized that this switch might be determined by AMP and the dominance of opposing effects: metabolism through AMP deaminase (AMPD2) (summer) and activation of AMP-activated protein kinase (AMPK) (winter). Liver samples were obtained from 13-lined ground squirrels at different times during the year, including summer and multiples stages of winter hibernation, and fat synthesis and β-fatty acid oxidation were evaluated. Changes in fat metabolism were correlated with changes in AMPD2 activity and intrahepatic uric acid (downstream product of AMPD2), as well as changes in AMPK and intrahepatic β-hydroxybutyrate (a marker of fat oxidation). Hepatic fat accumulation occurred during the summer with relatively increased enzymes associated with fat synthesis (FAS, ACL and ACC) and decreased enoyl CoA hydratase (ECH1) and carnitine palmitoyltransferase 1A (CPT1A), rate limiting enzymes of fat oxidation. In summer, AMPD2 activity and intrahepatic uric acid levels were high and hepatic AMPK activity was low. In contrast, the active phosphorylated form of AMPK and β-hydroxybutyrate both increased during winter hibernation. Therefore, changes in AMPD2 and AMPK activity were paralleled with changes in fat synthesis and fat oxidation rates during the summer-winter cycle. These data illuminate the opposing forces of metabolism of AMP by AMPD2 and its availability to activate AMPK as a switch that governs fat metabolism in the liver of hibernating ground squirrel.
机译:冬眠的动物在夏季活跃时会发展成脂肪肝,而在冬季会转变为脂肪氧化状态。我们假设这种转换可能是由AMP和相反作用的优势决定的:通过AMP脱氨酶(AMPD2)的代谢(夏季)和AMP激活的蛋白激酶(AMPK)的激活(冬季)。在一年中的不同时间(包括夏季和冬季冬眠的多个阶段)从13个衬里的松鼠中获取肝脏样品,并评估了脂肪合成和β-脂肪酸氧化。脂肪代谢的变化与AMPD2活性和肝内尿酸(AMPD2的下游产物)的变化以及AMPK和肝内β-羟基丁酸酯(脂肪氧化的标志物)的变化相关。夏季发生肝脏脂肪积累,与脂肪合成相关的酶(FAS,ACL和ACC)相对增加,烯酰辅酶A水合酶(ECH1)和肉碱棕榈酰转移酶1A(CPT1A)降低,这是脂肪氧化的限速酶。在夏季,AMPD2活性和肝内尿酸水平高,肝AMPK活性低。相反,在冬季冬眠期间,AMPK和β-羟基丁酸酯的活性磷酸化形式均增加。因此,在夏季和冬季,AMPD2和AMPK活性的变化与脂肪合成和脂肪氧化率的变化平行。这些数据阐明了AMPD2对AMP代谢的反作用力,以及激活AMPK作为控制冬眠地松鼠肝脏脂肪代谢的开关的有效性。

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