Literature search services are currently unavailable. During our hosting provider's UPS upgrade we experienced a hardware failure and are currently working to resolve the issue.

Preparing your results

Our searching services are busy right now. Your search will reload in five seconds.

Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Adipocyte-specific deficiency of angiotensinogen decreases plasma angiotensinogen concentration and systolic blood pressure in mice.

Previous studies demonstrated that overexpression of angiotensinogen (AGT) in adipose tissue increased blood pressure. However, the contribution of endogenous AGT in adipocytes to the systemic renin-angiotensin system (RAS) and blood pressure control is undefined. To define a role of adipocyte-derived AGT, mice with loxP sites flanking exon 2 of the AGT gene (Agt(fl/fl)) were bred to transgenic mice expressing Cre recombinase under the control of an adipocyte fatty acid-binding protein 4 promoter (aP2) promoter to generate mice with adipocyte AGT deficiency (Agt(aP2)). AGT mRNA abundance in adipose tissue and AGT secretion from adipocytes were reduced markedly in adipose tissues of Agt(aP2) mice. To determine the contribution of adipocyte-derived AGT to the systemic RAS and blood pressure control, mice were fed normal laboratory diet for 2 or 12 mo. In males and females of each genotype, body weight and fat mass increased with age. However, there was no effect of adipocyte AGT deficiency on body weight, fat mass, or adipocyte size. At 2 and 12 mo of age, mice with deficiency of AGT in adipocytes had reduced plasma concentrations of AGT (by 24-28%) compared with controls. Moreover, mice lacking AGT in adipocytes exhibited reduced systolic blood pressures compared with controls (Agt(fl/fl), 117 ± 2; Agt(aP2), 110 ± 2 mmHg; P < 0.05). These results demonstrate that adipocyte-derived AGT contributes to the systemic RAS and blood pressure control.

Pubmed ID: 22071160


  • Yiannikouris F
  • Karounos M
  • Charnigo R
  • English VL
  • Rateri DL
  • Daugherty A
  • Cassis LA


American journal of physiology. Regulatory, integrative and comparative physiology

Publication Data

January 15, 2012

Associated Grants

  • Agency: NCRR NIH HHS, Id: P20 RR021954
  • Agency: NCRR NIH HHS, Id: P20 RR021954-04
  • Agency: NCRR NIH HHS, Id: P20 RR021954-05
  • Agency: NCRR NIH HHS, Id: P20-RR-021954
  • Agency: NHLBI NIH HHS, Id: R01 HL073085
  • Agency: NHLBI NIH HHS, Id: R01 HL073085-08
  • Agency: NHLBI NIH HHS, Id: R01 HL073085-09
  • Agency: NHLBI NIH HHS, Id: R01-HL-073085
  • Agency: NHLBI NIH HHS, Id: T32-HL-091812

Mesh Terms

  • Adipocytes
  • Adiposity
  • Angiotensinogen
  • Animals
  • Blood Glucose
  • Blood Pressure
  • Body Weight
  • Female
  • Male
  • Mice
  • Mice, Transgenic
  • Renin-Angiotensin System