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Adipose tissue lipolysis and energy metabolism in early cancer cachexia in mice

机译:小鼠早期癌症恶病质中的脂肪组织脂肪分解和能量代谢

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Cancer cachexia is a progressive metabolic disorder that results in depletion of adipose tissue and skeletal muscle. A growing body of literature suggests that maintaining adipose tissue mass in cachexia may improve quality-of-life and survival outcomes. Studies of lipid metabolism in cachexia, however, have generally focused on later stages of the disorder when severe loss of adipose tissue has already occurred. Here, we investigated lipid metabolism in adipose, liver and muscle tissues during early stage cachexia - before severe fat loss - in the colon-26 murine model of cachexia. White adipose tissue mass in cachectic mice was moderately reduced (34-42%) and weight loss was less than 10% of initial body weight in this study of early cachexia. In white adipose depots of cachectic mice, we found evidence of enhanced protein kinase A - activated lipolysis which coincided with elevated total energy expenditure and increased expression of markers of brown (but not white) adipose tissue thermogenesis and the acute phase response. Total lipids in liver and muscle were unchanged in early cachexia while markers of fatty oxidation were increased. Many of these initial metabolic responses contrast with reports of lipid metabolism in later stages of cachexia. Our observations suggest intervention studies to preserve fat mass in cachexia should be tailored to the stage of cachexia. Our observations also highlight a need for studies that delineate the contribution of cachexia stage and animal model to altered lipid metabolism in cancer cachexia and identify those that most closely mimic the human condition.
机译:癌症恶病质是一种进行性代谢紊乱,导致脂肪组织和骨骼肌衰竭。越来越多的文献表明,维持恶病质的脂肪组织质量可能会改善生活质量和生存结果。然而,恶病质中脂质代谢的研究通常集中在已经发生严重脂肪组织损失的疾病后期。在这里,我们研究了结肠癌26恶病质鼠模型中,早期恶病质-严重脂肪损失之前-在脂肪,肝和肌肉组织中的脂质代谢。在早期恶病质的这项研究中,恶病质小鼠中的白色脂肪组织量适度减少(34-42%),体重减轻小于初始体重的10%。在恶病质小鼠的白色脂肪库中,我们发现增强的蛋白激酶A激活的脂解作用与增加的总能量消耗和棕色(而非白色)脂肪组织生热和急性期反应的标志物表达增加相吻合。在早期恶病质中,肝脏和肌肉中的总脂质没有变化,而脂肪氧化的标志物却增加了。这些初始代谢反应中的许多反应与恶病质后期的脂质代谢报道相反。我们的观察结果表明,针对恶病质保存脂肪量的干预研究应针对恶病质阶段进行。我们的观察结果还强调,需要进行研究以描述恶病质阶段和动物模型对癌症恶病质中脂质代谢改变的贡献,并确定与人类病情最相似的那些。

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