Hudgins Lisa C, Baday Aline, Hellerstein Marc K, Parker Thomas S, Levine Daniel M, Seidman Cynthia E, Neese Richard A, Tremaroli Jolanta D, Hirsch Jules
The Rogosin Institute, New York, NY 10021, USA.
J Nutr Biochem. 2008 Apr;19(4):237-45. doi: 10.1016/j.jnutbio.2007.02.013. Epub 2007 Jul 6.
Hepatic de novo lipogenesis (DNL) is markedly stimulated in humans by low-fat diets enriched in simple sugars. However, the dietary responsiveness of the key enzyme controlling DNL in human adipose tissue, fatty acid synthase (FAS), is uncertain.
Adipose tissue mRNA for FAS is increased in lean and obese subjects when hepatic DNL is elevated by a eucaloric, low-fat, high-sugar diet.
Twelve lean and seven obese volunteers were given two eucaloric diets (10% vs. 30% fat; 75% vs. 55% carbohydrate; sugar/starch 60/40) each for 2 weeks by a random-order cross-over design. FAS mRNA in abdominal and gluteal adipose tissues was compared to hepatic DNL measured in serum by isotopic and nonisotopic methods. Adipose tissue mRNA for tumor necrosis factor-alpha and IL-6, which are inflammatory cytokines that modulate DNL, was also assayed.
The low-fat high-sugar diet induced a 4-fold increase in maximum hepatic DNL (P<.001) but only a 1.3-fold increase in adipose tissue FAS mRNA (P=.029) and no change in cytokine mRNA. There was a borderline significant positive correlation between changes in FAS mRNA and hepatic DNL (P=.039). Compared to lean subjects, obese subjects had lower levels of FAS mRNA and higher levels of cytokine mRNA (P<.001).
The results suggest that key elements of human adipose tissue DNL are less responsive to dietary carbohydrate than is hepatic DNL and may be regulated by diet-independent factors. Irrespective of diet, there is reduced expression of the FAS gene and increased expression of cytokine genes in adipose tissues of obese subjects.
富含单糖的低脂饮食可显著刺激人体肝脏从头脂肪生成(DNL)。然而,人体脂肪组织中控制DNL的关键酶脂肪酸合酶(FAS)对饮食的反应性尚不确定。
当通过等热量、低脂、高糖饮食使肝脏DNL升高时,瘦人和肥胖受试者脂肪组织中FAS的mRNA会增加。
采用随机交叉设计,12名瘦志愿者和7名肥胖志愿者分别接受两种等热量饮食(脂肪含量分别为10%和30%;碳水化合物含量分别为75%和55%;糖/淀粉比例为60/40),每种饮食持续2周。将腹部和臀部脂肪组织中的FAS mRNA与通过同位素和非同位素方法测定的血清肝脏DNL进行比较。还检测了肿瘤坏死因子-α和IL-6的脂肪组织mRNA,这两种炎性细胞因子可调节DNL。
低脂高糖饮食使肝脏最大DNL增加了4倍(P<0.001),但脂肪组织FAS mRNA仅增加了1.3倍(P = 0.029),细胞因子mRNA无变化。FAS mRNA变化与肝脏DNL之间存在临界显著正相关(P = 0.039)。与瘦受试者相比,肥胖受试者的FAS mRNA水平较低,细胞因子mRNA水平较高(P<0.001)。
结果表明,人体脂肪组织DNL的关键成分对饮食碳水化合物的反应性低于肝脏DNL,并可能受饮食无关因素的调节。无论饮食如何,肥胖受试者脂肪组织中FAS基因表达降低,细胞因子基因表达增加。