High Sodium Intake Enhances Insulin-stimulated Glucose Uptake in Rat Epididymal Adipose Tissue
Article first published online: 6 SEP 2012
2008 North American Association for the Study of Obesity (NAASO)
Volume 16, Issue 6, pages 1186–1192, June 2008
How to Cite
Fonseca-Alaniz, M. H., Takada, J., Andreotti, S., De Campos, T. B.F., Campaña, A. B., Borges-Silva, C. N. and Lima, F. B. (2008), High Sodium Intake Enhances Insulin-stimulated Glucose Uptake in Rat Epididymal Adipose Tissue. Obesity, 16: 1186–1192. doi: 10.1038/oby.2008.69
- Issue published online: 6 SEP 2012
- Article first published online: 6 SEP 2012
- Received September 26, 2007; Accepted February 02, 2008
Objective: This study investigated the effect of different sodium content diets on rat adipose tissue carbohydrate metabolism and insulin sensitivity.
Methods and Procedures: Male Wistar rats were fed on normal- (0.5% Na+; NS), high- (3.12% Na+; HS), or low-sodium (0.06% Na+; LS) diets for 3, 6, and 9 weeks after weaning. Blood pressure (BP) was measured using a computerized tail-cuff system. An intravenous insulin tolerance test (ivITT) was performed in fasted animals. At the end of each period, rats were killed and blood samples were collected for glucose and insulin determinations. The white adipose tissue (WAT) from abdominal and inguinal subcutaneous (SC) and periepididymal (PE) depots were weighed and processed for adipocyte isolation and measurement of in vitro rates of insulin-stimulated 2-deoxy-d-[3H]-glucose uptake (2DGU) and conversion of -[U-14C]-glucose into 14CO2.
Results: After 6 weeks, HS diet significantly increased the BP, SC and PE WAT masses, PE adipocyte size, and plasma insulin concentration. The sodium dietary content did not influence the whole-body insulin sensitivity. A higher half-maximal effective insulin concentration (EC50) from the dose-response curve of 2DGU and an increase in the insulin-stimulated glucose oxidation rate were observed in the isolated PE adipocytes from HS rats.
Discussion: The chronic salt overload enhanced the adipocyte insulin sensitivity for glucose uptake and the insulin-induced glucose metabolization, contributing to promote adipocyte hypertrophy and increase the mass of several adipose depots, particularly the PE fat pad.