Journal of Applied Physiology
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J Appl Physiol 107: 794-800, 2009. First published July 9, 2009; doi:10.1152/japplphysiol.91062.2008
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Responses of LDL and HDL particle size and distribution to omega-3 fatty acid supplementation and aerobic exercise

Joshua S. Wooten, Kyle D. Biggerstaff, and Vic Ben-Ezra

Exercise Physiology Laboratory, Department of Kinesiology, Texas Woman's University, Denton, Texas

Submitted 6 August 2008 ; accepted in final form 5 July 2009

The purpose of this investigation was to determine the independent and combined effects of aerobic exercise and omega-3 fatty acid (n-3fa) supplementation on lipid and lipoproteins. Sedentary, normoglycemic, nonsmoking men (n = 11) were assigned to perform rest and exercise before and during n-3fa supplementation. Exercise consisted of 3 consecutive days of treadmill walking at 65% maximum O2 consumption for 60 min. Supplementation consisted of 42 days of 4.55 g/day of n-3fa. A two-way factorial ANOVA with repeated measures revealed significant reductions in total cholesterol (P = 0.001, –9.2%) and triglyceride (P = 0.007, –32.4%) concentrations postexercise. In addition, exercise increased LDL peak particle size (P = 0.001) from 26.2 to 26.4 nm, but not HDL size. The n-3fa supplementation resulted in a significant shift in the distribution of HDL-cholesterol (HDL-C) carried by HDL2b+2a (P = 0.001, 14.2%) and HDL3a+3b (P = 0.001, –22.8%), despite no significant changes in lipid and lipoprotein-cholesterol concentrations. The majority of the shift in HDL-C was noted in HDL2b (P = 0.001, 20.9%) and HDL3a (P < 0.001, –31.0%) particles. There were no combined effects of exercise and n-3fa supplementation on lipids and lipoproteins. Three consecutive days of aerobic exercise reduced triglyceride and total cholesterol concentrations with a concomitant increase in LDL peak particle size. In contrast, n-3fa supplementation shifted HDL-C from HDL3 particles to HDL2 particles, despite no significant changes in HDL2-C and HDL3-C concentrations. Exercise and n-3fa supplementation do not synergistically improve serum lipids and lipoproteins, but rather independently affect the metabolism of lipids and lipoproteins.

docosahexaenoic acids; eicosapentaenoic acids; lipoprotein-cholesterol



Address for reprint requests and other correspondence: J. S. Wooten, Baylor College of Medicine, Section of Atherosclerosis and Lipoprotein Research, Fondren/Brown M.S. A601, 6565 Fannin St., Houston, TX 77030 (e-mail: wooten{at}bcm.edu)







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