![]() |
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||



Centre for Advanced Food Studies,
* Department Human Nutrition, The Royal Veterinary and Agricultural University, DK-1958 Frederiksberg, Denmark;
Biocentrum-DTU, Biochemistry and Nutrition, Technical University of Denmark, Lyngby, Denmark;
** Section of Geriatrics and Clinical Nutrition Research, Faculty of Medicine, Uppsala University, Uppsala, Sweden; and
The Copenhagen City Heart Study, Bispebjerg University Hospital, Copenhagen, Denmark
3To whom correspondence should be addressed. E-mail: tth{at}kvl.dk.
There is a demand and need for healthy solid dietary fats. However, synthetic fats can be tailored to contain specific physiologic properties. Our goal was to design dietary solid test fats that would be both beneficial to the atherogenic lipid profile and stable against lipid peroxidation. Sixteen men (age 3575 y) substituted 80 g of their normal dietary fat intake with test fat for two periods of 21 d each in a double-blind, randomized, crossover study. Although solid, both test fats were low in cholesterol-raising SFA. Test fat "F" contained 5 g/100 g long chain (n-3) fatty acids matched by oleic acid in test fat "O." Plasma total triacylglycerol (TAG), VLDL TAG, cholesterol in VLDL, and intermediate density lipoproteins (IDL) were lower (P < 0.05), whereas apolipoprotein (apo) B of the large LDL-2 (d = 10311042 g/L) subclass, and cholesterol of HDL2b subclass, were higher after intake of F than O fat (P < 0.05). There was no difference in the effect on in vivo oxidation measured as the ratio of plasma isoprostanes F2 to arachidonic acid and urinary isoprostanes, whereas the vitamin E activity/plasma total lipids ratio was higher after intake of F than O (P = 0.008). In conclusion, a solid dietary fat containing (n-3) PUFA decreased plasma TAG, VLDL, and IDL cholesterol, and redistributed lipoprotein subclasses in LDL and HDL, with a higher concentration of the larger and less atherogenic subfractions. These changes took place without an increase in oxidative stress as measured by in vivo markers.
KEY WORDS: fish oil stearic acid LDL subclasses HDL subclasses oxidative stress
This article has been cited by other articles:
![]() |
M. J Caslake, E. A Miles, B. M Kofler, G. Lietz, P. Curtis, C. K Armah, A. C Kimber, J. P Grew, L. Farrell, J. Stannard, et al. Effect of sex and genotype on cardiovascular biomarker response to fish oils: the FINGEN Study Am. J. Clinical Nutrition, September 1, 2008; 88(3): 618 - 629. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. N. Mathur, K. R. Watt, and F. J. Field Regulation of intestinal NPC1L1 expression by dietary fish oil and docosahexaenoic acid J. Lipid Res., February 1, 2007; 48(2): 395 - 404. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Nalsen, B. Vessby, L. Berglund, M. Uusitupa, K. Hermansen, G. Riccardi, A. Rivellese, L. Storlien, A. Erkkila, S. Yla-Herttuala, et al. Dietary (n-3) Fatty Acids Reduce Plasma F2-Isoprostanes but Not Prostaglandin F2{alpha} in Healthy Humans J. Nutr., May 1, 2006; 136(5): 1222 - 1228. [Abstract] [Full Text] [PDF] |
||||