![]() |
|
|
Food Science Australia, North Ryde, Australia
Dear Editor:
A recent article by Lucas et al. (1
) prompts a comment on
the possible role of saponins in mediating the hypercholesterolemic
activity of soy protein. The hypercholesterolemic activity of soy
protein is now so well established that the U.S. Food and Drug
Administration has approved a coronary heart disease risk reduction
claim (2
). But, as Lucas et al. (1
) pointed
out, commercial soy protein typically contains high levels of saponins,
isoflavones and other phytochemicals that may in themselves influence
cholesterol metabolism (3
, 4
). So, it is perhaps
unfortunate that the health claim fails to specify a requirement for
these materials.
Lucas et al. (1
) reported that in Golden Syrian hamsters,
soy protein has no hypercholesterolemic activity after extraction with
ethanol, a treatment that would remove saponins, isoflavones and other
phytochemicals from the protein. They discussed the possible role of
isoflavones in mediating the hypercholesterolemic activity of soy
protein, while at the same time mentioning that this has recently been
questioned (5
). But, they did not discuss the possible
role of saponins.
The hypercholesterolemic activity of saponins has been well documented,
with clearly defined molecular mechanisms (6
). Saponins
are a structurally diverse group of triterpene or steroid glycosides.
The molecules are amphiphilic, the triterpene or steroid part being
hydrophobic and the sugar part hydrophilic, giving saponins their
characteristic surface activity from which the name is derived. There
seem to be two mechanisms by which saponins can affect cholesterol
metabolism:
Potter et al. (7
) suggested > 20 y ago
that the hypercholesterolemic action of soy protein is attributable to
the presence of saponins. Since then, it has been shown that isolated
soy saponins prevent dietary hypercholesterolemia in rats
(6
) and that whole soy flour increases fecal excretion of
bile acids compared with ethanol-extracted soy flour in rats
(6
) and humans (6
). Surprisingly, a search of
the literature (using Food Science and Technology Abstracts)
revealed only one report of a study of cholesterol metabolism in which
animals (in this case, rats) were fed highly purified soy protein
(8
). No hypercholesteolemic effect was observed with the
purified protein, although there were other metabolic effects. Clearly
much research remains to be done in this important area, particularly
in view of the health claims currently permitted for soy protein.
Manuscript received 24 May 2001. Revision accepted 9 August 2001.
LITERATURE CITED
1. Lucas, E. A., Khalil, D. A., Daggy, B. P. & Arjmandi, B. H. (2001) Ethanol-extracted soy protein isolate does not modulate serum cholesterol in golden Syrian hamsters: a model of postmenopausal hypercholesterolemia. J. Nutr. 131:211-214.
2. U.S. Food and Drug Administration (1999) Food Labeling Health Claims; Protein and Coronary Heart Disease; Final Rule. Federal Register 64 FR 57 October 26. U.S. Food and Drug Administration, Washington, DC. .
3. Fenwick, D. E. & Oakenfull, D. (1981) Saponin content of soya beans and some commercial soya bean products. J. Sci. Food Agric. 32:273-278.
4. Anderson, R. L. & Wolf, W. J. (1995) Compositional changes in trypsin inhibition, phytic acid, saponins and isoflavones related to soybean processing. J. Nutr. 125:581S-588S.
5. Greaves, K. A., Parks, J. S., Williams, J. K. & Wagner, J. D. (1999) Intact dietary soy protein, but not adding an isoflavone-rich soy extract to casein, improves plasma lipids in ovariectomized cynomologus monkeys. J. Nutr. 129:1585-1592.
6. Oakenfull, D. G. & Sidhu, G. S. (1990) Could saponins be a useful treatment for hypercholesterolaemia?. Eur. J. Clin. Nutr. 44:79-88.[Medline]
7. Potter, J. D., Topping, D. L. & Oakenfull, D. (1979) Soya, saponins and plasma cholesterol. Lancet i: 223. .
8. Madani, S., Prost, J. & Belleville, J. (2000) Dietary protein level and origin (casein and highly purified soybean protein) affect hepatic storage, plasma lipid transport, and antioxidative status in the rat. Nutrition 16:368-375.[Medline]
This article has been cited by other articles:
![]() |
N. R Matthan, S. M Jalbert, L. M Ausman, J. T Kuvin, R. H Karas, and A. H Lichtenstein Effect of soy protein from differently processed products on cardiovascular disease risk factors and vascular endothelial function in hypercholesterolemic subjects Am. J. Clinical Nutrition, April 1, 2007; 85(4): 960 - 966. [Abstract] [Full Text] [PDF] |
||||
![]() |
S.-O. Lee, A. L. Simons, P. A. Murphy, and S. Hendrich Soyasaponins Lowered Plasma Cholesterol and Increased Fecal Bile Acids in Female Golden Syrian Hamsters Experimental Biology and Medicine, July 1, 2005; 230(7): 472 - 478. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. A. Greany, J. A. Nettleton, K. E. Wangen, W. Thomas, and M. S. Kurzer Probiotic Consumption Does Not Enhance the Cholesterol-Lowering Effect of Soy in Postmenopausal Women J. Nutr., December 1, 2004; 134(12): 3277 - 3283. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Hu, M. B. Reddy, S. Hendrich, and P. A. Murphy Soyasaponin I and Sapongenol B Have Limited Absorption by Caco-2 Intestinal Cells and Limited Bioavailability in Women J. Nutr., August 1, 2004; 134(8): 1867 - 1873. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Song, S.-O. Lee, P. A. Murphy, and S. Hendrich Soy Protein With or Without Isoflavones, Soy Germ and Soy Germ Extract, and Daidzein Lessen Plasma Cholesterol Levels in Golden Syrian Hamsters Experimental Biology and Medicine, October 1, 2003; 228(9): 1063 - 1068. [Abstract] [Full Text] [PDF] |
||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||