Adipose depot-specific modulation of angiotensinogen gene expression in diet-induced obesity

Am J Physiol Endocrinol Metab. 2004 Jun;286(6):E891-5. doi: 10.1152/ajpendo.00551.2003. Epub 2004 Jan 28.

Abstract

Adipose tissue represents an important source of angiotensinogen (AGT). We investigated the effect of obesity induced by a high-fat diet on the expression of mouse (mAGT) and human AGT (hAGT) genes in liver, kidney, and heart and different adipose depots in normal mice (C57BL/6J), and in transgenic mice expressing the hAGT gene under the control of its own promoter. Mice were fed a high-fat diet (45% kcal) or normal chow (10% kcal) for 10 and 20 wk. The expression of mAGT and hAGT mRNA was quantified using an RNAse protection assay. Mice on the high-fat diet exhibited increased weight, fat mass, and plasma leptin. Expression of mAGT or hAGT genes was not affected by high-fat diet in nonadipose tissues, brown adipose tissue, or subcutaneous white fat. In contrast, high-fat diet increased both mAGT and hAGT gene expression in visceral adipose depots (omental, reproductive, and perirenal fat). Thus obesity-induced by a high-fat diet is associated with a tissue-specific increased expression of both mouse and human AGT genes in intra-abdominal adipose tissue. Our findings also suggest that 1.2 kb of regulatory sequences present in the hAGT transgene are sufficient to transcriptionally respond to a high-fat diet in an adipose-specific and depot-specific manner.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adipose Tissue / physiology*
  • Angiotensinogen / genetics*
  • Animals
  • Body Weight
  • Dietary Fats / pharmacology*
  • Gene Expression
  • Hypertension / physiopathology
  • Leptin / blood
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Obesity / physiopathology*
  • RNA, Messenger / analysis

Substances

  • Dietary Fats
  • Leptin
  • RNA, Messenger
  • Angiotensinogen