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Yin and Yang of hypothalamic insulin and leptin signaling in regulating white adipose tissue metabolism

机译:下丘脑胰岛素和瘦素信号传导的阴阳调节白脂肪组织代谢

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Fatty acids released from white adipose tissue (WAT) provide important energy substrates during fasting. However, uncontrolled fatty acid release from WAT during non-fasting states causes lipotoxicity and promotes inflammation and insulin resistance, which can lead to and worsen type 2 diabetes (DM2). WAT is also a source for insulin sensitizing fatty acids such as palmitoleate produced during de novo lipogenesis. Insulin and leptin are two major hormonal adiposity signals that control energy homeostasis through signaling in the central nervous system. Both hormones have been implicated to regulate both WAT lipolysis and de novo lipogenesis through the mediobasal hypothalamus (MBH) in an opposing fashion independent of their respective peripheral receptors. Here, we review the current literature on brain leptin and insulin action in regulating WAT metabolism and discuss potential mechanisms and neuro-anatomical substrates that could explain the opposing effects of central leptin and insulin. Finally, we discuss the role of impaired hypothalamic control of WAT metabolism in the pathogenesis of insulin resistance, metabolic inflexibility and type 2 diabetes.
机译:从白色脂肪组织(WAT)释放的脂肪酸在禁食期间提供了重要的能量底物。但是,在非禁食状态下从WAT中释放的不受控制的脂肪酸会引起脂毒性,并促进炎症和胰岛素抵抗,从而导致并加剧2型糖尿病(DM2)。 WAT还是从头脂肪形成过程中产生的胰岛素敏感性脂肪酸(如棕榈油酸酯)的来源。胰岛素和瘦素是两个主要的激素肥胖信号,它们通过中枢神经系统中的信号控制能量稳态。两种激素都被认为通过中下丘脑(MBH)以相反的方式调节WAT脂解和新生脂肪形成,而独立于其各自的外周受体。在这里,我们回顾了有关脑瘦素和胰岛素在调节WAT代谢中作用的最新文献,并讨论了可能解释中心瘦素和胰岛素的相反作用的潜在机制和神经解剖学底物。最后,我们讨论了下丘脑控制WAT代谢受损在胰岛素抵抗,代谢僵硬和2型糖尿病发病机理中的作用。

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