Chriett Sabrina, Pirola Luciano
Sabrina Chriett, Luciano Pirola, INSERM Unit 1060, South Lyon Hospital, Medical Faculty, CarMeN Laboratory, Lyon-1 University, INRA U1397, 69921 Oullins, France.
World J Biol Chem. 2015 Aug 26;6(3):223-30. doi: 10.4331/wjbc.v6.i3.223.
The increasing incidence of obesity worldwide and its related cardiometabolic complications is an urgent public health problem. While weight gain results from a negative balance between the energy expenditure and calorie intake, recent research has demonstrated that several small organic molecules containing a four-carbon backbone can modulate this balance by favoring energy expenditure, and alleviating endoplasmic reticulum stress and oxidative stress. Such small molecules include the bacterially produced short chain fatty acid butyric acid, its chemically produced derivative 4-phenylbutyric acid, the main ketone body D-β-hydroxybutyrate - synthesized by the liver - and the recently discovered myokine β-aminoisobutyric acid. Conversely, another butyrate-related molecule, α-hydroxybutyrate, has been found to be an early predictor of insulin resistance and glucose intolerance. In this minireview, we summarize recent advances in the understanding of the mechanism of action of these molecules, and discuss their use as therapeutics to improve metabolic homeostasis or their detection as early biomarkers of incipient insulin resistance.
全球肥胖症发病率的不断上升及其相关的心脏代谢并发症是一个紧迫的公共卫生问题。虽然体重增加是能量消耗与卡路里摄入之间负平衡的结果,但最近的研究表明,几种含有四碳骨架的小分子可以通过促进能量消耗、减轻内质网应激和氧化应激来调节这种平衡。这类小分子包括细菌产生的短链脂肪酸丁酸、其化学合成衍生物4-苯基丁酸、肝脏合成的主要酮体D-β-羟基丁酸以及最近发现的肌动蛋白β-氨基丁酸。相反,另一种与丁酸相关的分子α-羟基丁酸已被发现是胰岛素抵抗和葡萄糖不耐受的早期预测指标。在这篇小型综述中,我们总结了对这些分子作用机制理解的最新进展,并讨论了它们作为改善代谢稳态的治疗药物的用途,或作为早期胰岛素抵抗生物标志物的检测方法。