期刊
JOURNAL OF LIPID RESEARCH
卷 44, 期 11, 页码 2127-2134出版社
ELSEVIER
DOI: 10.1194/jlr.M300235-JLR200
关键词
sterol regulatory element binding protein 1c; carbohydrate response element binding protein; fatty acid synthase; messenger ribonucleic acid; acetyl-CoA carboxylase 1; stable isotopes
Lipogenesis is considered less active in human than in rat adipose tissue. This could be explained by different nutritional conditions, namely high-carbohydrate (HCHO) diet in rats and high-fat (HF) diet in humans. Adipose tissue was sampled (postabsorptive state) in rats and humans receiving HCHO or BY diets, ad libitum fed humans, and obese subjects. We measured 1) mRNA concentrations of fatty acid synthase (FAS), acetyl-CoA carboxylase 1 (ACC1), sterol regulatory element binding protein 1c (SREBP-1c), and carbohydrate response element binding protein (ChREBP), 2) SREBP-1c protein, and 3) FAS activity. FAS, ACC1, ChREBP, and SREBP1-c mRNA concentrations were unaffected by diet in humans or in rats. FAS and ACC1 mRNA levels were lower in humans than in rats (P < 0.05). FAS activity was unaffected by diet and was lower in humans (P < 0.05). SREBP-1c mRNA concentrations were similar in rats and humans, but the precursor and mature forms of SREBP-1c protein were less abundant in humans (P < 0.05). ChREBP mRNA concentrations were lower in humans than in rats.jlr In conclusion, the lipogenic capacity of adipose tissue is lower in humans than in rats. This is not related to differences in diet and is probably explained by lower abundance of SREBP-1c protein. A decreased expression of ChREBP could also play a role.-Letexier, D., C. Pinteur, V. Large, V Frering, and M. Beylot. Comparison of the expression and activity of the lipogenic pathway in human and rat adipose tissue..
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