ACE-modulated adiposity is related to higher energy expenditure and independent of lipolysis and glucose incorporation into lipids in adipocytes

• Published in: Physiological genomics Vol. 49; no. 12; pp. 712 - 721
• Main Authors: Fonseca-Alaniz, Miriam Helena, Higa, Talita Sayuri, Ferraz-de-Campos, Tarcila Beatriz, Takada, Julie, Torres-Leal, Francisco Leonardo, Evangelista, Fabiana Sant'Anna, Lima, Fabio Bessa, Krieger, José Eduardo
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.12.2017
• Subjects: ACE protein; Adipocytes; Adipose tissue; Adipose Tissue - metabolism; Adiposity - genetics; Adiposity - physiology; Angiotensin; Angiotensin II; Body weight; Carcasses; Energy expenditure; Energy Metabolism - genetics; Energy Metabolism - physiology; Fasting; Food intake; Gene dosage; Gene expression; Glucose; Glucose - metabolism; Laboratory testing; Lipids; Lipolysis; Peptidyl-dipeptidase A; Renin; Rodents; Transgenic mice; adipose tissue; lipogenesis; energy expenditure; lipolysis; ACE gene
• ISSN: 1094-8341; 1531-2267
• DOI: 10.1152/physiolgenomics.00056.2017

Emerging evidence suggests that both systemic and white adipose tissue-renin-angiotensin system components influence body weight control. We previously demonstrated that higher angiotensin-converting enzyme (ACE) gene expression is associated with lower body adiposity in a rodent model. In this study, we tested the hypothesis that a higher ACE gene dosage reduces fat accumulation by increasing energy expenditure and modulating lipolysis and glucose incorporation into lipids in adipocytes. After a 12 wk follow-up period, transgenic mice harboring three ACE (3ACE) gene copies displayed diminished WAT mass, lipid content in their carcasses, adipocyte hypotrophy, and higher resting oxygen uptake (V̇o ) in comparison with animals with one ACE gene copy (1ACE) after long fasting (12 h). No differences were found in food intake and in the rates of lipolysis and glucose incorporation into lipids in adipocytes. To assess whether this response involves increased angiotensin II type I receptor (AT1R) activation, AT1R blocker (losartan) was used in a separate group of 3ACE mice with body weight and adiposity comparable to that in the other 3ACE animals. We suggest that fasting-induced lower adiposity observed in animals with 3ACE gene copies might be associated with a higher expense of energy reserves; this response did not involve AT1R activation.