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产前低蛋白和产后高脂肪饮食通过诱导 Sprague Dawley 大鼠后代 Igf2 的表达来促进脂肪组织的快速生长。

Prenatal low-protein and postnatal high-fat diets induce rapid adipose tissue growth by inducing Igf2 expression in Sprague Dawley rat offspring.

机构信息

USDA Agricultural Research Service, Grand Forks Human Nutrition Research Center, Grand Forks, ND.

出版信息

J Nutr. 2013 Oct;143(10):1533-9. doi: 10.3945/jn.113.178038. Epub 2013 Aug 14.

Abstract

Maternal low-protein diets result in lower birth weight followed by accelerated catch-up growth that is accompanied by the development of obesity and glucose intolerance in later life. Whether postnatal high-fat (HF) diets further contribute to the development of obesity and insulin resistance in offspring by affecting adipose tissue metabolism and DNA methylation is currently unknown. Obese-prone Sprague-Dawley rats were fed 8% low protein (LP) or 20% normal protein diets for 3 wk prior to conception and throughout pregnancy and lactation to investigate whether prenatal LP and postnatal HF diets affect the rate of adipose tissue growth, insulin-like growth factor 2 (Igf2) expression, and DNA methylation in male offspring. At weaning, the offspring were fed 10% normal fat or 45% HF diets for 12 wk. The adipose tissue growth rate was increased (up to 26-fold) by the LP prenatal and HF postnatal diets. Adipose tissue Igf2 mRNAs and DNA methylation were increased by the LP prenatal and HF postnatal diets. The LP prenatal and HF postnatal diet increased the number of small adipocytes in adipose tissue and decreased insulin sensitivity. These findings suggest that prenatal LP and postnatal HF intake result in adipose tissue catch-up growth through alterations in the expression of the Igf2 gene and DNA methylation within adipocytes. These alterations in adiposity are accompanied by an increased risk of development of type 2 diabetes.

摘要

母体低蛋白饮食会导致出生体重降低,随后出现快速追赶性生长,从而导致成年后肥胖和葡萄糖不耐受。目前尚不清楚,高脂肪(HF)饮食是否会通过影响脂肪组织代谢和 DNA 甲基化,进一步导致后代肥胖和胰岛素抵抗的发生。肥胖易感的 Sprague-Dawley 大鼠在受孕前 3 周以及整个孕期和哺乳期,分别喂食 8%低蛋白(LP)或 20%正常蛋白饮食,以研究产前 LP 和产后 HF 饮食是否会影响雄性后代脂肪组织生长速度、胰岛素样生长因子 2(Igf2)表达和 DNA 甲基化。在断奶时,后代分别喂食 10%正常脂肪或 45% HF 饮食 12 周。LP 产前和 HF 产后饮食会增加脂肪组织生长速度(增加 26 倍)。LP 产前和 HF 产后饮食增加了脂肪组织中 Igf2 mRNA 和 DNA 甲基化。LP 产前和 HF 产后饮食增加了脂肪组织中小脂肪细胞的数量,并降低了胰岛素敏感性。这些发现表明,产前 LP 和产后 HF 摄入通过改变脂肪细胞中 Igf2 基因的表达和 DNA 甲基化,导致脂肪组织的追赶性生长。这些脂肪量的改变伴随着 2 型糖尿病发生风险的增加。

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