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Role of hypothalamic de novo ceramides synthesis in obesity and associated metabolic disorders

机译:下丘脑的作用在肥胖症和相关代谢障碍中的合成

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Background Sphingolipid-mediated signalling pathways are described as important players in the normal functioning of neurons and nonneuronal cells in the central nervous system (CNS). Scope of review This review aims to show role of de novo ceramide synthesis in the CNS in controling key physiological processes, including food intake, energy expenditure, and thermogenesis. The corollary is a condition that leads to a dysfunction in ceramide metabolism in these central regions that can have major consequences on the physiological regulation of energy balance. Major conclusions Excessive hypothalamic de novo ceramide synthesis has been shown to result in the establishment of central insulin resistance, endoplasmic reticulum stress, and inflammation. Additionally, excessive hypothalamic de novo ceramide synthesis has also been associated with changes in the activity of the autonomic nervous system. Such dysregulation of hypothalamic de novo ceramide synthesis forms the key starting point for the initiation of pathophysiological conditions such as obesity – which may or may not be associated with type 2 diabetes.
机译:背景技术鞘磷脂介导的信号传导途径被描述为中枢神经系统(CNS)中神经元和非对细胞正常功能的重要参与者。审查范围本综述旨在显示De Novo神经酰胺合成在CNS中控制关键生理过程的作用,包括食物摄入,能源支出和热生成。必然结果是导致这些中央区域中神经酰胺代谢的功能障碍,这可能对能量平衡的生理调节产生重大影响。主要结论已经显示出过量的下丘氨酸透明酰胺合成导致建立中央胰岛素抵抗,内质网胁迫和炎症。另外,过量的下丘脑DE Novo神经酰胺合成也与自主神经系统的活性的变化有关。下丘脑DE Novo神经酰胺合成的这种缺点形成了发酵病理学病症的关键起点,例如肥胖症 - 这可能或可能与2型糖尿病有关。

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