![]() |
|
|
Manuscript received 3 July 1997. Initial reviews completed 15 August 1997. Revision accepted 15 October 1997.
Foster Biomedical Research Laboratory, Brandeis University, Waltham, MA 02254
The imbalance that develops between low-density lipoprotein (LDL) production and clearance during saturated fat consumption is responsible for expanding the circulating LDL pool. To assess the imbalance attributable to fatty acids alone, i.e., without the interaction of dietary cholesterol, the most fat-sensitive species available (the gerbil) was challenged with either a 12:0+14:0 rich-fat (high coconut, low safflower) or high 18:2 (high safflower, low coconut) fat for 4-5 wks. The plasma lipoprotein cholesterol profile, including lipoprotein composition, particle size and 125I-LDL turnover were measured. Although total plasma cholesterol (TC) was threefold higher with saturated fatty acid (SFA) feeding (230 vs. 70 mg/100 mL; 5.9 ± 0.1 vs. 1.8 ± 0.05 mmol/L, P < 0.0001) and LDL cholesterol (LDL-C) was fivefold greater (10 vs. 54 mg/100 mL; 0.26 ± 0.02 vs. 1.4 ± 0.02 mmol/L, P < 0.001), the high-density lipoprotein (HDL2) fraction increased the most (27 vs. 79 mg/100 mL; 0.7 ± 0.02 vs. 2.0 ± 0.1 mmol/L, P < 0.05) with minimal HDL3 (NS) difference (16 vs. 26 mg/100 mL; 0.43 ± 0.08 vs. 0. 7 ± 0.05 mmol/L). Particle composition and size did not differ between groups. LDL kinetic analyses revealed that the fractional catabolic rate did not differ between gerbils with these extreme fat intakes, implicating overproduction and not reduced clearance as the primary consideration in LDL expansion. Thus SFA-induced cholesterolemia can be severe in the absence of dietary cholesterol with a greater impact on high-density lipoprotein than LDL and without an appreciable role attributed to LDL clearance (receptors).
Key words: gerbils, LDL, LDL kinetics, LDL receptor activity, saturated fat.
The Journal of Nutrition Vol. 128 No. 3 March 1998,
pp. 477-484
Copyright ©1998 by the American Society for Nutritional Sciences
This article has been cited by other articles:
![]() |
A. Ohta, M. Uehara, K. Sakai, M. Takasaki, H. Adlercreutz, T. Morohashi, and Y. Ishimi A Combination of Dietary Fructooligosaccharides and Isoflavone Conjugates Increases Femoral Bone Mineral Density and Equol Production in Ovariectomized Mice J. Nutr., July 1, 2002; 132(7): 2048 - 2054. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Uehara, A. Ohta, K. Sakai, K. Suzuki, S. Watanabe, and H. Adlercreutz Dietary Fructooligosaccharides Modify Intestinal Bioavailability of a Single Dose of Genistein and Daidzein and Affect Their Urinary Excretion and Kinetics in Blood of Rats J. Nutr., March 1, 2001; 131(3): 787 - 795. [Abstract] [Full Text] |
||||
![]() |
K. Hayes Medium-chain triacylglycerols may not raise cholesterol Am. J. Clinical Nutrition, December 1, 2000; 72(6): 1583 - 1583. [Full Text] [PDF] |
||||
![]() |
T. Morohashi, T. Sano, A. Ohta, and S. Yamada True Calcium Absorption in the Intestine Is Enhanced by Fructooligosaccharide Feeding in Rats J. Nutr., October 1, 1998; 128(10): 1815 - 1818. [Abstract] [Full Text] |
||||