Desai Mina, Ferelli Monica, Kallichanda Natash, Lane Robert H
Perinatal Research Laboratories, Department of Obstetrics and Gynecology, David-Geffen School of Medicine at University of California, Los Angeles, CA 90502, USA.
Reprod Sci. 2008 Oct;15(8):785-96. doi: 10.1177/1933719108318597.
As enhanced adipogenesis contributes to programmed obesity, adipogenic and lipogenic signaling pathways in intrauterine growth restricted (IUGR) offspring were examined. From 10 days to term gestation, rats received ad libitum food (control) or were 50% food-restricted (IUGR). Pups were nursed and weaned to ad libitum diet. mRNA and protein levels of adipogenic transcription factors and lipid enzymes (1 day and 9 month) and adipocyte cell size (3 weeks and 9 months) were determined. One day-old IUGR males showed upregulation of peroxisome proliferator-activated receptor (PPAR gamma(2)), including upstream factors regulating PPAR gamma, and RXR alpha, with which PPAR gamma heterodimerizes. Intracellular lipolytic enzyme (hormone-sensitive lipase) was downregulated. Nine-month-old IUGR males showed upregulation of adipogenic and lipogenic (SREBP1c) transcription factors with upregulation of enzymes facilitating fatty acid uptake (lipoprotein lipase) and synthesis (fatty acid synthase), leading to hypertrophic adipocytes. Paradoxical upregulation of adipogenesis signaling cascade prior to the development of obesity in IUGR males suggests early changes in signaling mechanisms.
由于增强的脂肪生成会导致程序性肥胖,因此对宫内生长受限(IUGR)后代的脂肪生成和脂肪生成信号通路进行了研究。从妊娠第10天到足月,大鼠自由进食(对照)或食物限制50%(IUGR)。幼崽哺乳并断奶后自由饮食。测定了脂肪生成转录因子和脂质酶的mRNA和蛋白质水平(1天和9个月)以及脂肪细胞大小(3周和9个月)。1日龄IUGR雄性大鼠的过氧化物酶体增殖物激活受体(PPARγ(2))上调,包括调节PPARγ的上游因子和与PPARγ异二聚化的RXRα。细胞内脂解酶(激素敏感性脂肪酶)下调。9月龄IUGR雄性大鼠的脂肪生成和脂肪生成(SREBP1c)转录因子上调,促进脂肪酸摄取(脂蛋白脂肪酶)和合成(脂肪酸合酶)的酶上调,导致脂肪细胞肥大。IUGR雄性大鼠在肥胖发生之前脂肪生成信号级联的反常上调表明信号机制的早期变化。