Molecular Biology, Nutrition and Biotechnology (Nutrigenomics), University of the Balearic Islands (UIB), Palma de Mallorca 07122, Spain.
J Nutr Biochem. 2010 Jan;21(1):23-33. doi: 10.1016/j.jnutbio.2008.10.001. Epub 2009 Jan 20.
The aim of this study was to analyze regional differences in the time-course response to fasting and refeeding in the expression of genes involved in lipid metabolism in retroperitoneal, mesenteric and inguinal adipose tissue. Rats were studied under different feeding conditions: feeding state; after 4, 8 or 24 h of fasting; and after 3 h of refeeding following 8 h of fasting. The expression of lipogenesis-related genes decreased by fasting in adipose tissue, and the retroperitoneal depot showed the fastest response: mRNA levels of peroxisome proliferator-activated receptor gamma 2 (PPARgamma2) decreased after 4 h of fasting and those of sterol regulatory element binding protein 1c (SREBP1c), fatty acid synthase (FAS), GPAT and glucose transporter 4 (GLUT4) decreased after 8 h. In the inguinal depot, mRNA levels of SREBP1c, acetyl-coenzyme A carboxylase alpha, FAS and lipoprotein lipase decreased after 8 h of fasting, while in the mesenteric depot, only GLUT4 and FAS mRNA levels decreased after 8 and 24 h, respectively. Concerning lipolytic and fatty acid oxidation genes, only adipose triglyceride lipase and carnitine palmitoyltransferase 1a expression increased after 24 h of fasting in the retroperitoneal depot. Three hours of refeeding restored the expression of the lipogenic transcription factors PPARgamma2 and SREBP1c in the retroperitoneal depot and of PPARgamma2 in the inguinal depot. This period of refeeding was ineffective in changing the expression of genes related with lipid mobilization and fatty acid oxidation, except hormone-sensitive lipase, whose expression decreased in the mesenteric depot. It is suggested that different regulations of the expression of genes related with lipid metabolism between internal and subcutaneous depots to feeding and fasting conditions are site-specific metabolic features of white adipose tissue.
本研究旨在分析在禁食和再喂养过程中,参与脂肪代谢的基因表达的时间进程在腹部、肠系膜和腹股沟脂肪组织中的区域差异。在不同的喂养条件下对大鼠进行了研究:喂养状态;禁食 4、8 或 24 小时后;禁食 8 小时后再喂养 3 小时。脂肪组织中与脂肪生成相关的基因在禁食后表达减少,腹膜后脂肪垫的反应最快:过氧化物酶体增殖物激活受体γ 2(PPARγ2)mRNA 水平在禁食 4 小时后下降,固醇调节元件结合蛋白 1c(SREBP1c)、脂肪酸合酶(FAS)、甘油磷酸酰基转移酶和葡萄糖转运蛋白 4(GLUT4)mRNA 水平在禁食 8 小时后下降。在腹股沟脂肪垫中,SREBP1c、乙酰辅酶 A 羧化酶α、FAS 和脂蛋白脂肪酶的 mRNA 水平在禁食 8 小时后下降,而在肠系膜脂肪垫中,只有 GLUT4 和 FAS 的 mRNA 水平分别在禁食 8 小时和 24 小时后下降。关于脂肪分解和脂肪酸氧化基因,只有脂肪甘油三酯脂肪酶和肉碱棕榈酰转移酶 1a 的表达在腹膜后脂肪垫中禁食 24 小时后增加。再喂养 3 小时恢复了腹膜后脂肪垫中脂肪生成转录因子 PPARγ2 和 SREBP1c 的表达,以及腹股沟脂肪垫中 PPARγ2 的表达。这段再喂养时间对与脂质动员和脂肪酸氧化相关基因的表达没有影响,除了激素敏感脂肪酶,其在肠系膜脂肪垫中的表达下降。这表明,内部和皮下脂肪组织对喂养和禁食条件的脂肪代谢相关基因表达的不同调节是白色脂肪组织的特定部位代谢特征。