Addition of n-3 fatty acids to a 4-hour lipid infusion does not affect insulin sensitivity, insulin secretion, or markers of oxidative stress in subjects with type 2 diabetes mellitus
Received 5 April 2009; accepted 16 June 2009. published online 28 August 2009.
Abstract
Fatty acids (FA) can impair glucose metabolism to a varying degree depending on time of exposure and also of type of FA. Here we tested for acute effects of marine n-3 FA on insulin sensitivity, insulin secretion, energy metabolism, and oxidative stress. This was a randomized, double-blind, crossover study in 11 subjects with type 2 diabetes mellitus. A 4-hour lipid infusion (Intralipid [Fresenius Kabi, Halden, Norway], total of 384 mL) was compared with a similar lipid infusion partly replaced by Omegaven (Fresenius Kabi) that contributed a median of 0.1 g fish oil per kilogram body weight, amounting to 0.04 g/kg of marine n-3 FA. Insulin sensitivity was assessed by isoglycemic hyperinsulinemic clamps; insulin secretion (measured after the clamps), by C-peptide glucagon tests; and energy metabolism, by indirect calorimetry. Infusion of Omegaven increased the proportion of n-3 FA in plasma nonesterified fatty acids (NEFA) compared with Intralipid alone (20:5n-3: median, 1.5% [interquartile range, 0.6%] vs −0.2% [0.2%], P = .001; 22:6n-3: 0.8% [0.4%] vs −0.7% [0.2%], P = .001). However, glucose utilization was not affected; neither was insulin secretion or total energy production (P = .966, .210, and .423, respectively, for the differences between the lipid clamps). Omegaven tended to lower oxidation of fat (P = .062) compared with Intralipid only, correlating with the rise in individual n-3 NEFA (r = 0.627, P = .039). The effects of clamping on phospholipid FA composition, leptin, adiponectin, or F2-isoprostane concentrations were not affected by Omegaven. Enrichment of NEFA with n-3 FA during a 4-hour infusion of Intralipid failed to affect insulin sensitivity, insulin secretion, or markers of oxidative stress in subjects with type 2 diabetes mellitus.
aDivision of Clinical Nutrition, Department of Clinical Service, St. Olavs Hospital, Trondheim, Norway
bDepartment of Cancer Research and Molecular Medicine, Faculty of Medicine, Norwegian University of Science and Technology, Trondheim, Norway
cDepartment of Medical Biochemistry, St. Olavs Hospital, Trondheim, Norway
dDepartment of Public Health and Caring Sciences, Faculty of Medicine, Oxidative Stress and Inflammation, Uppsala University, Uppsala Science Park, Uppsala, Sweden
eOxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford, UK
fDivision of Endocrinology, Department of Medicine, St. Olavs Hospital, Trondheim, Norway
Corresponding author. Division of Clinical Nutrition, Department of Clinical Service, St. Olavs Hospital, N-7006 Trondheim, Norway. Tel.: +47 72571310; fax: +47 72571203.
The work was done at St. Olavs Hospital, Trondheim, Norway.
The local ethics committee approved the study protocol. All participants gave written informed consent.