Fifteen healthy men (aged 26.0±3.1 years, BMI 23.8±1.9 kg/m2), were enrolled. Subjects were randomised to 3–4 weeks of oral FO supplementation (7.2 g/day, providing 1.1 g/day of 20:5(n-3) and 0.7 g/day of 22:6 (n-3) fatty acids) or no supplementation and then submitted to endotoxin challenge: 2 ng/kg of LPS. All subjects were studied twice (placebo and LPS). Measurements: vital signs, energy expenditure (EE), glucose and lipid metabolism (2H2-glucose), plasma cytokines and stress hormones for 6 h after LPS or placebo.
LPS caused cytokine release, fever, increases in heart rate, resting EE and substrate oxidation, plasma glucagon and glucose concentrations; the neuro-endocrine response was characterised by increased plasma stress hormones. FO significantly blunted fever, ACTH and cortisol plasma levels (no effect on cytokine release). FO blunted the peak norepinephrine after LPS.
FO supplements blunted the endocrine stress response and the increase in body temperature, but had no impact on cytokine production after LPS. These findings conflict with the postulated anti-inflammatory effects of FO on arachidonic acid metabolism and cytokine release. These results suggest that FO may exert beneficial effects in sepsis though non-inflammatory which require further investigations