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游离脂肪酸受体4调控能量代谢的途径与分子机制 被引量:5

Pathways and Molecular Mechanism of Free Fatty Acid Receptor 4 in Metabolism Regulation
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摘要 游离脂肪酸(FFA)是调节机体能量代谢的重要物质,可通过胞内代谢所产生的中间产物或在胞外激活细胞膜上G蛋白偶联受体调节代谢。FFA受体4(FFAR4)是FFA激活的一种膜受体,表达于下丘脑、胃肠道、脂肪、肝脏和舌等多种与物质代谢相关的组织,可影响激素和细胞因子等分泌,通过多个途径调节机体代谢过程,包括影响下丘脑摄食中枢活动,调节胃肠内分泌,改变脂肪细胞状态,参与肝脏代谢,影响味觉和食物喜好等。FFAR4激动剂可通过以上作用增加机体能量消耗,有望用于肥胖和2型糖尿病的治疗。 Free fatty acids( FFA) are important in regulating energy metabolism,and they regulate body metabolism not only by intracellular metabolism but also by activating the G-protein coupled receptor on the extracellular membrane. FFA receptor 4( FFAR4) is a membrane receptor activated by FFA,which is expressed in hypothalamus,gastrointestinal tract,fat,liver and tongue and other tissues related to body metabolism,which can affect the secretion of hormones and cytokines,regulate the metabolic process of the body through many ways,including affecting the activity of feeding center of hypothalamus,regulating gastrointestinal endocrine,changing the state of fat cells,and participating in liver metabolism,thereby affecting taste and food preference,etc. FFAR4 agonists are able to increase energy consumption through the above mentioned function and are expected as the candidates for the therapy of obesity and diabetes.
作者 任晓莹 梁向艳 刘媛 李亚 赵玉峰 REN Xiaoying;LIANG Xiangyan;LIU Yuan;LI Ya;ZHAO Yufeng(Institute of Basic Medical Sciences,Department of Basic Medical Sciences,Xi′an Medical College,Xi′an 710021,China;Department of Endocrinology,the First Affiliated Hospital,Xi′an Medical College,Xi′an 710077,China)
出处 《医学综述》 2020年第4期636-640,共5页 Medical Recapitulate
基金 国家自然科学基金(81700370) 西安市科技计划项目(201805094YX2SF28(12))。
关键词 能量代谢 游离脂肪酸 游离脂肪酸受体4 Energy metabolism Free fatty acid Free fatty acid receptor 4
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  • 1张瑞,谢欣,王明伟.游离脂肪酸受体的结构、分布及功能[J].生命的化学,2005,25(2):92-94. 被引量:2
  • 2龚珍,贺凌燕,柳红,刘景根,朱维良,陈凯先,蒋华良.一个潜在的糖尿病新靶标——GPR40[J].生命科学,2006,18(5):467-472. 被引量:4
  • 3Rompler H, Hofreiter M, Schoneberg T, et al. G proteincoupled time travel: evolutionary aspects of GPCR research. Mol Interv, 2007, 7(1): 17-25
  • 4Wettschureck N, Offermarms S. Mammalian G proteins and their cell type specific functions. Physiol Rev, 2005, 85(4): 1159-204
  • 5Katsuma S, Hatae N, Tsujimoto G, et al. Free fatty acids inhibit serum deprivation-induced apoptosis through GPR120 in a murine enteroendocrine cell line STC- 1. J Biol Chem, 2005, 280(20): 19507-15
  • 6Madiraju SRM, Poitout V. G protein-coupled receptors and insulin secretion: 119 and counting. Endocrinology, 2007, 148(6): 2598-600
  • 7Wang JH, Simonavicius N, Ling L, et al. Medium-chain fatty acids as ligands for orphan G protein-coupled receptor GPR84. J Biol Chem, 2006, 281(45): 34457-64
  • 8Matsumura S, Inoue K, Fushiki T, et al. GPR expression in the rat taste bud relating to fatty acid sensing. Biomed Res, 2007, 28(1): 49-55
  • 9Doyle M E, Egan JM. Mechanisms of action of glucagon-like peptide 1 in the pancreas. Pharmacol Ther, 2007, 113 (3): 546-93
  • 10Combettes MMJ. GLP-1 and type 2 diabetes: physiology and new clinical advances. Curr Opin Pharmacol, 2006, 6 (6): 598-605

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