Camargo Antonio, Meneses Maria E, Perez-Martinez Pablo, Delgado-Lista Javier, Jimenez-Gomez Yolanda, Cruz-Teno Cristina, Tinahones Francisco J, Paniagua Juan A, Perez-Jimenez Francisco, Roche Helen M, Malagon Maria M, Lopez-Miranda Jose
Lipids and Atherosclerosis Unit, IMIBIC, Reina Sofia University Hospital, University of Cordoba, Av. Menendez Pidal, s/n, Córdoba, Spain.
Eur J Nutr. 2014;53(2):617-26. doi: 10.1007/s00394-013-0570-2. Epub 2013 Aug 7.
Adipose tissue is now recognized as a highly active metabolic and endocrine organ. Our aim was to investigate the effect of the dietary fat on the two main adipose tissue functions, endocrine and lipid store, by analyzing the adipose tissue gene expression from metabolic syndrome patients.
A randomized, controlled trial conducted within the LIPGENE study assigned 39 metabolic syndrome patients to 1 of 4 isoenergetic diets: (1) high-saturated fatty acid (HSFA), (2) high-monounsaturated fatty acid (HMUFA), (3) low-fat, high-complex carbohydrate diet supplemented with long-chain n-3 fatty acids (LFHCC n-3), and (4) low-fat, high-complex carbohydrate diet supplemented with placebo (LFHCC), for 12 weeks each. A fat challenge reflecting the fatty acid composition as the original diets was conducted post-intervention.
The long-term consumption of HSFA, LFHCC, and LFHCC n-3 diets, but not HMUFA diet, decreased the perilipin fasting mRNA levels. LFHCC diet consumption increased fasting FABP4 expression, while it was reduced by the consumption of LFHCC n-3 diet. LFHCC meal reduced, while LFHCC n-3 meal intake increased postprandial CAV1 expression.
The quantity and quality of dietary fat induce differential lipid storage and processing related gene expression, which may interact with the expression of adipokines through common regulatory mechanisms.
脂肪组织如今被认为是一个高度活跃的代谢和内分泌器官。我们的目的是通过分析代谢综合征患者的脂肪组织基因表达,来研究膳食脂肪对脂肪组织的两种主要功能(内分泌和脂质储存)的影响。
在LIPGENE研究中进行了一项随机对照试验,将39名代谢综合征患者分配到4种等能量饮食中的一种:(1)高饱和脂肪酸(HSFA),(2)高单不饱和脂肪酸(HMUFA),(3)补充长链n-3脂肪酸的低脂、高复合碳水化合物饮食(LFHCC n-3),以及(4)补充安慰剂的低脂、高复合碳水化合物饮食(LFHCC),每种饮食持续12周。干预后进行了一项反映原始饮食脂肪酸组成的脂肪挑战。
长期食用HSFA、LFHCC和LFHCC n-3饮食,但不包括HMUFA饮食,会降低禁食状态下围脂滴蛋白的mRNA水平。食用LFHCC饮食会增加禁食状态下FABP4的表达,而食用LFHCC n-3饮食则会使其降低。LFHCC餐会降低餐后CAV1的表达,而LFHCC n-3餐的摄入则会增加其表达。
膳食脂肪的数量和质量会诱导不同的脂质储存和加工相关基因表达,这些基因表达可能通过共同的调节机制与脂肪因子的表达相互作用。