n-3 PUFA have shown potential anti-
obesity and
insulin-sensitising properties. However, the mechanisms involved are not clearly established. The aim of the present study was to assess the effects of EPA administration, one of the
n-3 PUFA, on
body-weight gain and adiposity in rats fed on a standard or a high-fat (cafeteria) diet. The actions on white adipose tissue lipolysis, apoptosis and on several genes related to
obesity and
insulin resistance were also studied. Control and cafeteria-induced
overweight male Wistar rats were assigned into two subgroups, one of them daily received EPA ethyl
ester (1 g/kg) for 5 weeks by
oral administration. The high-fat diet induced a very significant increase in both
body weight and fat mass. Rats fed with the cafeteria diet and orally treated with EPA showed a marginally lower
body-weight gain (P = 0.09), a decrease in food intake (P < 0.01) and an increase in
leptin production (P < 0.05). EPA administration reduced retroperitoneal adipose tissue weight (P < 0.05) which could be secondary to the inhibition of the adipogenic
transcription factor PPARgamma gene expression (P < 0.001), and also to the increase in apoptosis (P < 0.05) found in rats fed with a control diet.
TNFalpha gene expression was significantly increased (P < 0.05) by the cafeteria diet, while EPA treatment was able to prevent (P < 0.01) the rise in this inflammatory
cytokine. Adiposity-corrected
adiponectin plasma levels were increased by EPA. These actions on both
TNFalpha and
adiponectin could explain the beneficial effects of EPA on
insulin resistance induced by the cafeteria diet.