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饮食诱导的肥胖以及C57BL/6J和ICAM-1缺陷小鼠肝脏基因表达的改变。

Diet-induced obesity and hepatic gene expression alterations in C57BL/6J and ICAM-1-deficient mice.

作者信息

Gregoire Francine M, Zhang Qin, Smith Steven J, Tong Carmen, Ross David, Lopez Henry, West David B

机构信息

Pfizer Global R&D, Alameda, California 94502, USA.

出版信息

Am J Physiol Endocrinol Metab. 2002 Mar;282(3):E703-13. doi: 10.1152/ajpendo.00072.2001.

Abstract

The effects of high-fat feeding on the development of obesity were evaluated in intercellular adhesion molecule-1 (ICAM-1) knockout and C57BL/6J (B6) male mice fed a high-fat diet for < or =50 days. Serum and tissues were collected at baseline and after 1, 11, and 50 days on the diet. After 11 days on the diet, ICAM-1-deficient, but not B6, mice developed fatty livers and showed a significant increase in inguinal fat pad weight. At day 50, ICAM-1-deficient mice weighed less, and their adiposity index and circulating leptin levels were significantly lower than those of B6 controls. To better understand the early differential response to the diet, liver gene expression was analyzed at three time points by use of Affymetrix GeneChips. In both strains, a similar pattern of gene expression was detected in response to the high-fat diet. However, sterol regulatory element-binding protein-1, apolipoprotein A4, and adipsin mRNAs were significantly induced in ICAM-1-deficient livers, suggesting that these genes and their associated pathways may be involved in the acute diet response observed in the knockout mice.

摘要

在喂食高脂饮食≤50天的细胞间黏附分子-1(ICAM-1)基因敲除雄性小鼠和C57BL/6J(B6)雄性小鼠中,评估高脂喂养对肥胖发生发展的影响。在饮食干预的基线期以及第1天、第11天和第50天后收集血清和组织。饮食干预11天后,ICAM-1基因缺陷小鼠(而非B6小鼠)出现脂肪肝,且腹股沟脂肪垫重量显著增加。在第50天,ICAM-1基因缺陷小鼠体重较轻,其肥胖指数和循环瘦素水平显著低于B6对照组。为了更好地理解对饮食的早期差异反应,利用Affymetrix基因芯片在三个时间点分析肝脏基因表达。在两种品系中,均检测到对高脂饮食有相似的基因表达模式。然而,在ICAM-1基因缺陷小鼠的肝脏中,固醇调节元件结合蛋白-1、载脂蛋白A4和脂肪酶的mRNA显著上调,表明这些基因及其相关途径可能参与了基因敲除小鼠中观察到的急性饮食反应。

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