Professional Documents
Culture Documents
Original Communication
Received for publication: May 11, 2009; Accepted for publication: January 19, 2010
Abstract: Soy isoflavones have been reported to decrease the risk of atherosclerosis in postmenopausal
women. However, the effects of dietary consumption of soybean have not been explored. In this study,
we evaluated the effects of consuming yellow soybeans, black soybeans (Glycine max), or sword beans
(Canavalia gladiate) on lipid and oxidative stress levels in an ovariectomized rat model. Forty-seven
nine-week-old female rats were ovariectomized, randomly divided into four groups, and fed one of the
following diets for 10 weeks: a diet supplemented with casein (NC, n = 12), a diet supplemented with
yellow soybean (YS, n = 12), a diet supplemented with black soybean (BS, n = 12), or a diet supple-
mented with sword bean (SB, n = 11). Plasma triglyceride (TG) levels in the BS and SB groups were
significantly lower than that in the NC group. Notably, the BS group had significantly lower plasma
total cholesterol (TC), and low-density lipoprotein cholesterol (LDL-C) levels than the other groups.
Hepatic total lipid levels were significantly lower in the YS and SB groups, and cholesterol levels were
significantly lower in the SB group than in the NC group. Superoxide dismutase (SOD) and catalase
(CAT) activities were significantly higher in the groups fed beans compared to the NC group. Hepatic
thiobarbituric acid reactive substances (TBARS) levels were also significantly lower in the BS and SB
groups than the NC group. In conclusion, our results suggest that consumption of various types of beans
may inhibit oxidative stress in postmenopausal women by increasing antioxidant activity and improving
lipid profiles. Notably, intake of black soybean resulted in the greatest improvement in risk factors
associated with cardiovascular disease.
Key words: Yellow soybean, black soybean, sword bean, lipid metabolism, antioxidant enzyme activities.
DOI 10.1024/0300–9831/a000010 Int. J. Vitam. Nutr. Res., 80 (2), 2010, © Hogrefe & Huber Publishers
98 J.S. Byun et al.: Effect of Various Beans on Lipid Metabolism
Int. J. Vitam. Nutr. Res., 80 (2), 2010, © Hogrefe & Huber Publishers
J.S. Byun et al.: Effect of Various Beans on Lipid Metabolism 99
xylazine (45 mg/kg b.w.). The abdominal area was to decrease their trypsin-inhibiting activity. After cool-
sterilized with 75 % ethanol and opened by a surgical ing, beans were converted to powder using a 60 mesh.
operation. The uterus and ovaries were taken out, and Each diet was prepared by mixing various quantities
only the ovary was ligated and cut off. Then, the uterus of the powdered beans with the AIN-93M-based diet.
and adipose tissue were put back into the abdomen The yellow soybean, black soybean, and sword bean
and sewn up. The OVX rats were randomly divided powders accounted for 35 %, 35 %, and 50 % of the
into four groups and fed one of four diets: a casein diet experimental diet, respectively, to ensure isonitroge-
without soybean addition (NC group, n = 12), a yellow neous contents (15 %). Since each bean has a different
soybean diet (YS group, n = 12), a black soybean diet protein content (34.4 % for yellow soybean, 35.2 % for
(BS group, n = 12), or a sword bean diet (SB group, black soybean, and 22.7 % for sword bean). Thus, the
n = 11) for 10 weeks. The beans were purchased from protein source in the diet was either casein or whole
a local market and autoclaved for 16 minutes at 121 °C soy powder (Table I). All diets were isonitrogeneous
and isocaloric, and the energy ratio of carbohydrates
to proteins to lipids was adjusted to be 65:15:20, re-
Table I: Compositions of casein, yellow soybean, black spectively. All rats received water and food ad libitum.
soybean and sword bean (g/100 g edible portion). The composition of the normal experimental diet is
Ingredients Water Protein Fat Carbohydrate
provided in Table II. During the experimental period,
body weight was measured once per week and food
1)
Casein 0.96 98.3 0.05 0.63 intake was measured three times a week. All animals
Yellow soybean2) 9.6 34.4 18.6 28.4 were housed and cared for in accordance with the US
National Institutes of Health (NIH) Guide for the
Black soybean3) 11.0 35.2 18.2 26.4 Care and Use of Laboratory Animals.
Sword bean4) 10.4 22.7 3.2 52.2
1)
Lactic Acid Caseins (Nice Ltd., Ukraine)
Sample collection
2)
Powdered yellow soybean was autoclaved and dried
3)
Powdered black soybean was autoclaved and dried At the end of the experimental period, the rats were
4)
Powdered sword bean was autoclaved and dried deprived of food overnight and sacrificed under ethyl
Int. J. Vitam. Nutr. Res., 80 (2), 2010, © Hogrefe & Huber Publishers
100 J.S. Byun et al.: Effect of Various Beans on Lipid Metabolism
ether anesthesia. Blood samples were collected im- filtration of extracts, the collected solution was cen-
mediately into heparin-coated sterile tubes by car- trifuged at 3,000 × g for 10 minutes. The chloroform
diac puncture. Plasma was obtained from the blood phase was collected and vacuum-concentrated. Total
samples by centrifugation (4000 × g for 10 minutes) at lipids were estimated by gravimetric analysis. The
4 °C and stored at –70 °C until further analysis. The liver cholesterol concentrations were measured using
livers were removed, washed with cold saline, patted a commercial diagnostic kit (SIMENSE Germany).
between paper towels, weighed, and then stored at
–70 °C for laboratory analysis.
Hepatic antioxidant enzyme activities
Plasma lipid profiles Two grams of liver tissue were homogenized in 10 mL
of a 0.25 M sucrose buffer, then the homogenates
The concentrations of triglycerides (TG), total cho- were centrifuged at 600 × g for 10 minutes to remove
lesterol (TC), high-density lipoprotein cholesterol the nuclear fraction, and the remaining separated
(HDL-C), and low-density lipoprotein cholesterol supernatant was centrifuged at 10,000 × g for 20
(LDL-C) were measured using a commercial diag- minutes to collect the mitochondrial fraction for a
nostic kit (SIMENSE Germany Co, UK) and a pho- catalase (CAT) assay. The supernatant was ultra-
tometric autoanalyzer (ADVIA 2400, Japan). The centrifuged at 105,000 × g for 1 hour to isolate the
TC and TG levels in the plasma were estimated by cytosolic fraction for the superoxide dismutase (SOD)
the COD-POD method and the GK-GPO method, assay. SOD activity was estimated according to the
respectively. The HDL-C level in plasma was deter- method of Marklund and Marklund [29], which uses
mined after precipitation of apoB-containing lipopro- a color change due to auto-oxidation of pyrogallol.
teins by sodium phosphotungstate and MgCl2. The One unit (U) of enzyme activity was calculated as the
LDL-C level in plasma was calculated using Friede- protein content inhibiting 50 % of the auto-oxidation
wald’s formulation [27]. of pyrogallol without an enzyme source. SOD activ-
ity was expressed as U/mg protein. CAT activity was
measured by the disappearance rate of H2O2 moni-
Liver lipid profiles tored spectrophotometrically at 240 nm according
to the method of Aebi with slight modification [30].
Total lipids in the liver were extracted according to the One unit (U) of enzyme activity was defined as the
Folch method [28]. One gram of liver tissue was ho- amount of enzyme catalyzing 1 μmol of H2O2 per
mogenized with chloroform/methanol (2:1, v/v), and minute at 25 °C. The CAT activity was expressed as
then 2 mL of ice-cold distilled water was added. After U/mg protein.
Table III: The effects of various bean types on body weight, weight gain, food intake, and liver weight in ovariectomized
rats*.
Variables Groups
NC YS BS SB
Body weight (g)
Initial 164.83 ± 2.05NS 164.66 ± 2.83 164.08 ± 2.78 163.45 ± 1.42
a b b
Final 322.08 ± 11.69 288.75 ± 7.88 287.25 ± 9.70 221.40 ± 2.07c
Weight gain (g/day) 1.70 ± 0.12a 1.34 ± 0.08b 1.33 ± 0.11b 0.61 ± 0.02c
Food intake (g/day) 12.65 ± 0.33a 11.18 ± 0.19b 11.06 ± 0.35b 9.96 ± 0.05c
NS
Liver weight (g/100 g b.w.) 2.29 ± 0.09 2.48 ± 0.11 2.31 ± 0.07 2.25 ± 0.07
*
Data are expressed as mean ±S.E.M. of 11 to 12 rats per group. Values in the same row with different superscripts (a,
b, and c) are significantly different at a p-value less than 0.05 by one-way ANOVA and Duncan’s multiple-range test.
NS: Not significant
NC: ovariectomized rats fed a casein diet
YS: ovariectomized rats fed a yellow soybean diet
BS: ovariectomized rats fed a black soybean diet
SB: ovariectomized rats fed a sword bean diet
Int. J. Vitam. Nutr. Res., 80 (2), 2010, © Hogrefe & Huber Publishers
J.S. Byun et al.: Effect of Various Beans on Lipid Metabolism 101
Table IV: The effects of various bean types on plasma TG, TC, HDL-C, and LDL-C levels in ovariectomized rats* (mg/dL)..
Variables Groups
NC YS BS SB
a ab b
TG 54.58 ± 4.79 46.58 ± 4.29 36.75 ± 1.73 40.72 ± 2.60b
TC 53.36 ± 4.40a 40.33 ± 2.70b 27.50 ± 3.19c 34.54 ± 3.38bc
a b c
LDL-C 7.83 ± 0.68 6.50 ± 0.92 3.58 ± 0.65 4.54 ± 0.63bc
HDL-C 9.69 ± 0.54NS 10.51 ± 0.49 10.30 ± 0.90 11.02 ± 0.62
*
Data are expressed as mean ±S.E.M. of 11 to 12 rats per group. Values in the same row with different superscripts (a,
b, and c) are significantly different at a p-value less than 0.05 by one-way ANOVA and Duncan’s multiple-range test.
NS: Not significant
NC: ovariectomized rats fed a casein diet
YS: ovariectomized rats fed a yellow soybean diet
BS: ovariectomized rats fed a black soybean diet
SB: ovariectomized rats fed a sword bean diet
Int. J. Vitam. Nutr. Res., 80 (2), 2010, © Hogrefe & Huber Publishers
102 J.S. Byun et al.: Effect of Various Beans on Lipid Metabolism
cholesterol levels were not significantly different be- weight gain in rats fed various bean diets is probably
tween the YS and BS groups. due to the lower food intake of these rats compared
Superoxide dismutase (SOD) and catalase (CAT) ac- to rats fed casein diets. In addition to the lowest food
tivities were higher in the groups fed yellow soybean, intake, the SB group had the lowest body weight gain
black soybean, or sword bean than in the untreated among the various bean groups. This may be due to
control group (Table VI). Notably, SOD activities a difference in the taste and smell of the SB-supple-
were generally higher in the YS and BS groups than mented diet compared to the other experimental diets.
in the NC group. CAT activity was generally higher In previous studies [32, 33], levels of various lipids
in the groups fed various bean types than in the NC were significantly higher in OVX rats than in sham-
group, but there were no significant differences in operated rats. In fact, because of the possibility that
CAT activity among the various bean-fed groups. an ovariectomy might in itself increase the levels of
Hepatic TBARS levels were lower in the groups fed various lipids, we did not include a sham group in
beans than in the NC group. The SB group, and in our study. In this study, rats fed various bean types
particular the BS group, had lower TBARS levels showed a decrease in plasma TG, TC, and LDL-C
than the NC group. levels compared with the NC group. Plasma TG levels
in the BS and SB groups were significantly lower than
in the NC group. Both plasma TC and LDL-C levels
in the groups fed beans were significantly lower than
Discussion those in the NC group. Notably, the BS group had
the lowest plasma TC and LDL-C levels among the
We investigated the effects of consumption of three various bean-fed groups. Hepatic total lipid and total
bean types on lipid levels, lipid peroxidation, and an- cholesterol levels were also significantly lower in the
tioxidant enzyme activities in ovariectomized rats, various bean groups than in the NC group. Notably,
an animal model of the postmenopausal condition hepatic total lipid levels were significantly lower in
characterized by ovarian hormone deficiency. The the YS and SB groups, and hepatic total cholesterol
lipid profiles, lipid peroxidation levels, and antioxidant levels were significantly lower in the SB group, than
enzyme activities of OVX rats fed a diet supplemented the NC group.
with yellow soybeans, black soybeans, or sword beans Sirtori et al. [34] and Descovich et al. [35] found
were evaluated and compared with those of rats fed that diets high in soy protein (all animal protein re-
a casein diet. The parameters measured above are placed) substantially reduced blood LDL cholesterol
risk factors for cardiovascular disease, particularly by 20~30 % in animals with severe hypercholester-
atherosclerosis. olemia. When soy protein is substituted for animal
Rats in the NC group showed the greatest weight protein, hypercholesterolemia does not occur. Thus,
gain and food intake, followed by rats in the YS and either casein diets have a direct hypercholesterolemic
BS groups, and finally rats in the SB group. The re- action, or soy protein diets have a cholesterol-lowering
sults of this study indicate that consumption of beans action. In our study, consumption of various beans
significantly reduced body weight gain and food intake resulted in a decrease in levels of TG, TC, and LDL-
compared to consumption of casein. The lower body C. The soy protein contents of the experimental diets
Table V: The effects of various bean types on hepatic lipid profiles in ovariectomized rats*.
Variables Groups
NC YS BS SB
Lipid profiles (mg/g wet liver)
Total lipids 50.87 ± 9.07a 32.83 ± 2.37b 40.49 ± 3.75ab 29.88 ± 2.79b
Total cholesterol 4.84 ± 0.21a 4.53 ± 0.20ab 4.65 ± 0.16ab 4.16 ± 0.17b
*
Data are expressed as mean ± S.E.M. of 11 to 12 rats per group. Values in the same row with different superscripts (a,
b, and c) are significantly different at a p-value less than 0.05 by one-way ANOVA and Duncan’s multiple-range test.
NS: Not significant
NC: ovariectomized rats fed a casein diet
YS: ovariectomized rats fed a yellow soybean diet
BS: ovariectomized rats fed a black soybean diet
SB: ovariectomized rats fed a sword bean diet
Int. J. Vitam. Nutr. Res., 80 (2), 2010, © Hogrefe & Huber Publishers
J.S. Byun et al.: Effect of Various Beans on Lipid Metabolism 103
Table VI: The effects of various bean types on hepatic SOD and CAT activity and TBARS levels in ovariectomized rats*.
variables Groups
NC YS BS SB
Antioxidant status
SOD (U/mg protein) 3.44 ± 0.05b 3.82 ± 0.06a 3.82 ± 0.13 a 3.59 ± 0.05ab
CAT (U/mg protein) 22.75 ± 0.48b 26.87 ± 1.08a 30.10 ± 1.25a 28.23 ± 1.78a
Oxidant status TBARS
(nmol/g wet liver) 8.53 ± 0.49a 7.12 ± 0.33ab 5.10 ± 0.60c 6.29 ± 0.49bc
*
Data are expressed as mean ± S.E.M. of 11 to 12 rats per group. Values in the same row with different superscripts (a,
b, and c) are significantly different at a p-value less than 0.05 by one-way ANOVA and Duncan’s multiple-range test.
NC: ovariectomized rats fed a casein diet
YS: ovariectomized rats fed a yellow soybean diet
BS: ovariectomized rats fed a black soybean diet
SB: ovariectomized rats fed a sword bean diet
were the same (15 %) and the isoflavone contents of the reduction in lipids observed after the consump-
the experimental beans were similar (0.25 % for yel- tion of BS. Although the cholesterol-lowering effects
low soybean, 0.27 % for black soybean, and 0.22 % of soybeans are widely accepted, the mechanism(s)
for sword bean). Postmenopausal women are gener- underlying these effects is not well understood, but
ally at higher risk for cardiovascular disease because is postulated to be due to soy proteins, isoflavones,
ovarian hormone deficiency is associated with elevat- and anthocyanins, as well as other components [9, 13].
ed levels of circulating TC and LDL-C. In previous In addition, soybeans contain a wide range of phyto-
studies, dietary supplementation with soybean iso- chemicals that are currently being investigated. It is
flavones significantly decreased plasma TC, TG, and possible that the various phytochemicals interact syn-
especially LDL-C levels, and significantly increased ergistically to lower cholesterol. Our results suggest
HDL-C levels [36]. We hypothesize that the various that consumption of various types of beans, namely
isoflavone-containing beans investigated in this study soybeans and sword beans, has a beneficial effect on
may have lowered plasma cholesterol levels by their lipid profiles in OVX rats, as indicated by decreased
estrogenic activity. TG, TC, and LDL-C levels in both the blood and liver.
However, this hypocholesterolemic effect is not Antioxidant enzymes such as SOD and CAT can
simply an estrogenic effect, because soybeans are also effectively convert superoxide radicals to molecular
rich in anthocyanins and other phytochemicals. An- H2O2 and oxygen, and can consecutively decompose
thocyanins play important roles as dietary antioxidants H2O2 to molecular water and oxygen [41]. In fact, CAT
in the prevention of oxidative damage, and can reduce and SOD are capable of eliminating lipid peroxidation
the risk of coronary heart disease [37,38]. Black soy- products and reactive oxygen species (ROS), thereby
beans have a stronger anti-oxidative effect than yellow directly protecting cells and tissues from deleterious
soybeans and sword beans. The anti-oxidative activity radicals [42].
of dark-colored soybeans may be higher than those of Ozgocmen et al. [43] reported that postmenopausal
light-colored soybeans [39]. In our study, the rats fed women appeared to have increased oxidative stress as
BS had lower plasma TG, TC, and LDL-C levels than evidenced by high MDA levels and low CAT activity,
the rats fed YS or SB. Although the different beans suggesting that lack of estrogen had a pro-oxidant
had similar isoflavone and soy protein contents, the effect due to an increase in free radical formation.
differential result may be because the BS seed coat Increased oxidative stress and reduced bioavailabil-
contains higher quantities of anthocyanins than the ity of antioxidants may induce oxidative damage in
SB and YS seed coats. LDL oxidation is one of the postmenopausal woman and OVX rats. In this study,
more well-studied free radical-mediated processes. SOD and CAT activities were higher in the groups
Oxidized LDL is responsible for the pathogenesis of fed various types of beans than the NC group. Our
atherosclerosis that can lead to the build-up of plaque results are consistent with previous studies that dem-
in arteries [40]. Therefore, consumption of food rich onstrated that various types of beans had antioxidant
in antioxidants may protect against cardiovascular capacity both in vivo and in vitro [44, 45]. The protec-
disease. Anthocyanins in BS appear to contribute to tive roles of various beans against oxidative damage
Int. J. Vitam. Nutr. Res., 80 (2), 2010, © Hogrefe & Huber Publishers
104 J.S. Byun et al.: Effect of Various Beans on Lipid Metabolism
in OVX rats might be due to their ability to decrease soybeans may protect against cardiovascular disease
lipid oxidation, as it is known that isoflavones have and atherosclerosis. Further studies are required to
antioxidant activity [46]. However, SOD and CAT determine the potential implications of the consump-
activities were not significantly different between the tion of sword beans on lipid metabolism.
bean-fed groups in our study. Phytochemicals may act
by different mechanisms to defend against harmful
free radicals. Recently, soybeans have attracted atten-
tion because of their strong antioxidant, anti-cancer, References
and anti-inflammation effects [26]. Based on these
results, we hypothesize that consumption of sword 1. Law, M.R. and Wald, N.J. (1994) An ecological study
bean as well as yellow soybean and black soybean of serum cholesterol and ischaemic heart disease
can increase the activities of antioxidant enzymes in between 1950 and 1990. Europ. J. Clin. Nutr. 48, 305.
postmenopausal women. Further studies are needed 2. Cai, Y.Y., Khoo, L.P. and Xiong, Z.W. (2003)
to confirm this hypothesis. Developing a Web-enabled and graphics-enhanced
Hepatic TBARS levels are commonly used to as- collaborative environment for integrated research of
sess lipid peroxidation and oxidative stress [47]. In this cardiovascular and atherosclerotic clinical biology.
study, hepatic TBARS levels were the lowest in the BS Int. Conference on Cyberworlds 2003, 92.
group, followed by the SB and YS groups, and highest
3. Penn, M.S. and Chisolm, G.M. (1994) Oxidized
in the NC group. Soy isoflavones can directly quench
lipoproteins, altered cell function and atherosclerosis.
free radicals, though they may also decrease oxidative Atherosclerosis 108, 21.
damage through indirect mechanisms such as induc-
tion of cellular antioxidant- scavenging enzymes [48]. 4. Devi, G.S., Prasad, M.H., Saraswathi, I., Raghu,
The different hepatic TBARS levels in rats fed vari- D., Rao, D.N. and Reddy, P.P. (2000) Free radicals
ous types of bean may be due to the different levels of antioxidant enzymes and lipid peroxidation in dif-
isoflavones and anthocyanins in the beans. Notably, the ferent types of leukemias. Clin. Chim. Acta 293, 53.
strong effect of black soybean on hepatic TBARS levels 5. Isles, C.G., Hole, D.J. Hawthorne, V.M. and Lever,
may be related to the high anthocyanin content of this A.F. (1992) Relation between coronary risk and
type of bean. Anthocyanins may prevent the copper- coronary mortality in women of the Renfrew and
induced oxidation of LDL by both metal-chelating and Paisley survey: comparison with men. Lancet 339,
radical scavenging mechanisms [49]. Kowalczyk et al. 702.
[50] demonstrated that anthocyanin supplementation
6. Barrett, C.E. and Bush, T.L. (1991) Estrogen and
decreased hepatic TBARS levels and increased antioxi- coronary heart disease in women-reply. J. Am. Med.
dant activity in animals. Oxidative stress is associated Assoc. 266, 1358.
with cholesterol accumulation and foam cell formation,
which are the hallmarks of early atherosclerosis in vas- 7. Rosano, G.M., Vitale, C., Marazzi, G. and Volterrani,
cular tracts [51]. Anthocyanins can thus protect against M. (2007) Menopause and cardiovascular disease: the
oxidative damage and reduce the risk of coronary heart evidence. Climacteric 10, 19.
disease [52]. Overall, consumption of various beans had 8. Lewis, S. (2007) Do endocrine treatments for breast
a beneficial effect on antioxidant enzyme activities in cancer have a negative impact on lipid profiles and
OVX rats, as indicated by increased SOD and CAT cardiovascular risk in postmenopausal women? Am.
activities, and by decreased TBARS levels. Heart J. 153, 182.
In conclusion, our results suggest that consump-
9. Food labeling: health claims: soy protein and coronary
tion of beans containing soy protein and various an-
heart disease. (1999) Food and Drug Administration,
tioxidant micronutrients may inhibit oxidative stress HHS: final rule: soy protein and coronary heart
in postmenopausal women by enhancing antioxidant disease. Fed Reg. 64, 57700.
activity and decreasing levels of harmful lipids. These
effects are likely to be mediated by soy proteins, isofla- 10. Erdman, J.W. Jr. and Potter, S.M. (1997) Soy and
vones, anthocyanins, and other phytochemicals pres- bone health. The Soy Connection 5, 1.
ent in these beans. Notably, intake of black soybeans, 11. Chiechi, L.M., Secreto, G., D’Amore, M., Fanelli,
which contain the highest anthocyanin levels, resulted M., Venturelli, E., Cantatore, F., Valerio, T., Laselva,
in the greatest improvement in risk factors associated G. and Loizze, P. (2002) Efficacy of a soy rich diet in
with atherosclerosis and cardiovascular disease. Fur- preventing postmenopausal osteoporosis: The Menfis
thermore, sword beans as well as yellow and black randomized trial. Maturitas 42, 295.
Int. J. Vitam. Nutr. Res., 80 (2), 2010, © Hogrefe & Huber Publishers
J.S. Byun et al.: Effect of Various Beans on Lipid Metabolism 105
12. Coward, L., Barnes, N.C., Setchell, K.D.R. and disease. National Academy of Sciences of the United
Barnes, S. (1993) Genistein, daidzein and their States of America. 92, 7460.
β-glycoside conjugates: antitumor isoflavones in
soybean foods from American and Asian diets. J. 24. Purseglove, J.W. (1968) Canavalia gladiate (Jacq.)
Agr. Food Chem. 41, 1961. D.C. in tropical crops: Dicotyledons. 1, 245.
13. Anderson, R.L. and Wolf, W.J. (1995) Compositional 25. Spoladore, D.S. and Teixeria, J.P.F. (1987) Chemical
changes in trypsin inhibitors, phytic acid, saponins composition of seeds of canavalia gladiate D.C.
and isoflavones related to soybean processing. J. Bragantia. 46, 133.
Nutr. 125, 581(s).
26. Morris, J.B. (2007) Swordbean (Canavalia ensiformis
14. Khosla, P., Samman, S. and Carroll, K.K. (1991) (L.) genetic resources regenerated for potential
Decreased receptor-mediated LDL catabolism in medical, nutraceutical and agricultural traits. Genetic
casein-fed rabbits precedes the increase in plasma Resources and Group Evolution. 54, 585.
cholesterol levels. J. Nutr. Biochem. 2, 203.
27. Friedewald, W.T., Levy, R.I. and Fredrickson, D.S.
15. Wiseman, H., Lim, P. and O‘Reilly, J. (1996) (1972) Estimation of the concentration of low density
Inhibition of liposomal lipid peroxidation by lipoprotein cholesterol in plasma, without use of the
isoflavonoid-type phyto-oestrogens from soybeans of preparative ultracentrifuge. Clinical Chemistry 18,
different countries of origin. Biochem. Soc. Trans. 24, 499.
392.
28. Folch, J., Lees, M. and Sloan-Stanley, G.H. (1966) A
16. Sreeram, N.P., Schutzki, R., Chandra, A. and Nair, simple method for isolation and purification of total
M.G. (2002) Characterization, quantification, and lipids from animal tissues. J. Biol. Chem. 266, 497.
bioactivities of anthocyanins in Cornus species. J.
Agric. Food Chem. 50, 2519. 29. Marklund, S. and Marklund, G. (1974) Involvement
of the superoxide anion radical in the autoxidation
17. Bermudez, M.J. and Tomas-Barberan, F.A. (2004) of pyrogallol and a convenient assay for superoxide
Evaluation of commercial red fruit juice concentrates dismutase. European Journal of Biochemistry 47,
as ingredients for antioxidant functional juices. Eur. 467.
Food Res. Technol. 219, 133.
30. Aebi, H. (1984) Catalase in vitro. Methods
18. Einbond, L.S., Reynertson, K.A., LUO, X.D., Enzym. 105, 121.
Basile, M.J. and Kennelly, E.J. (2004) Anthocyanin
antioxidants from edible fruits. Food Chem. 84, 23. 31. Ohkawa, H., Ohishi, N. and Yagi, K. (1979) Assay
for lipid peroxides in animal tissues by thiobarbituric
19. The Korean Nutritional Society (1989) The status of acid reaction. Analytical Biochemistry 95, 351.
food and nutrition consumption. pp. 98, 100, Korean
Nutritional Resource Data, Shin-Kwang Publishing 32. Lee, B.H., Lee, H.H., Kim, J.H., Cho, B.R. and
Co., Seoul. Choi, Y.S. (2007) Effects of a soluble fraction of
soybean on lipid profiles in ovariectomized rats fed a
20. Inagaki, S., Morimura, S. and Shigematsu, T. (2005) cholesterolemic diet. J. Med. Food 10, 521.
Apoptosis induction by vinegar produced from boiled
extract of black soybeans in human monoblastic 33. Gossell-Williams, M., Lyttle, K., Clarke, T., Gardner,
leukemia U937 cells: difference in sensitivity to cell M. and Simon, O. (2008) Supplementation with
toxicity compared to normal lymphocytes. Food pumpkin seed oil improves plasma lipid profile
Science and Technology Research 11, 311. and cardiovascular outcomes of female non-
ovariectomized and ovariectomized Sprague-Dawley
21. Kim, J. and Jeon, J.R. (2005) Quality characteristics rats. Phytother. Res. 22, 873.
of tofu added with black soybean hull powder. J. Kor.
Soc. Food Cult. 20, 633. 34. Sirtori, C.R., Gatti, E., Mantero, O., Conti, F.,
Agradi, E., Sirtori, M., Fraterrigo, L, Tavazzi L.
22. Azevedo, L., Gomes, J.C. and Stringheta, P.C. (2003) and Kritchevsky, D. (1979) Clinical experience
Black bean (Phaseolus vulgaris L.) as a protective with the soybean protein diet in the treatment of
agent against DNA damage in mice. Food Chem. hypercholesterolemia. Am. J. Clin. Nutr. 32, 1645.
Tox. 41, 1671.
35. Descovich, G.C., Ceredi, C., Gaddi, A., Benassi,
23. Walzem, R.L., Watkins, S. and Frankel, E.N. (1995) M.S., Mannino, G., Colombo, L., Cattin, L., Fontana,
Older plasma lipoproteins are more susceptible G., Senin, U., Mannarino, E., Caruzzo, C., Bertelli,
to oxidation: a linking mechanism for the lipid and E., Fragiacomo, C., Noseda, G., Senin, M. and
oxidation theories of atherosclerotic cardiovascular Sirtori, C.R. (1980) Multicentre study of soybean
Int. J. Vitam. Nutr. Res., 80 (2), 2010, © Hogrefe & Huber Publishers
106 J.S. Byun et al.: Effect of Various Beans on Lipid Metabolism
protein diet for outpatient diet for outpatient hyper- 46. Oh, H.Y., Lim, S.Y., Lee, J.M., Kim, D.Y., Ann, E.S.
cholesterolemic patients. Lancet 2, 709. and Yoon, S. A. (2007) Combination of soy isoflavone
supplementation and exercise improves lipid profiles
36. Reynolds, K., Chin, A. and Lees, K.A. (2006) A meta- and protects antioxidant defense-systems against
analysis of the effect of soy protein supplementation exercise-induced oxidative stress in ovariectomized
on serum lipids. Am. J. Cardi. 98, 633. rats. Bio. Factors. 29, 175.
37. Drenska, D., Bantutova, I. and Ovcharov, R. 47. Beltowski, J., Wojcicka, G., Gorny, D. and Marciniak,
(1989) Anticonvulsant effect of anthocyanins and A. (2000) The effect of dietary-induced obesity on
antioxidants. Fomatsiya (Sofia) 39, 33. lipid peroxidation, antioxidant enzymes and total
plasma antioxidant capacity. J. Physiol. Pharmacol. 5,
38. Satue-Gracia, M.T., Heinonen, M. and Frankel, E.N.
883.
(1997) Anthocyanins as antioxidants on human low-
density lipoprotein and lecithin-liposome systems. J. 48. Wei, H., Cai, Q. and Rahn, R.O. (1996) Inhibition
Agric. Food Chem. 45, 3362. of UV light- and Fenton reaction-induced
oxidative DNA damage by the soybean isoflavone
39. Bae, E.A. and Moon, G.S. (1997) A study on the
antioxidative activities of Korean soybeans. J. genistein. Carcinogenesis 17, 73.
Korean Soc. Food Sci. Nutr. 26, 203. 49. Dorman, H.J.D., Peltoketo, A., Hiltumen, L. and
40. Steinberg, D. (1997) Low-density lipoprotein Tikkanen, M.J. (2003) Characterisation of the
oxidation and its pathobiological significance. J. Bio. antioxidant properties of de-odourised aqueous
Chem. 272, 34. extracts from selected Lamiaceae herbs. Food
Chem. 83, 255.
41. Yang, Z., Jie, G. and Dong, F. (2008) Radical-
scavenging abilities and antioxidant properties of 50. Kowalczyk, E., Kopff, A., Niedworok, J., Kopff, M.
theaflavins and their gallate esters in H2O2-mediated and Jankowski, A. (2002) Anthocyanins–an adjunct
oxidative damage system in the HPF-1 cells. to cardiovascular therapy? Kardiologia Polska 57, 332.
Toxicology in Vitro 22, 1250.
51. Glass, C.K. and Witztum, J.L. (2001) Atherosclerosis:
42. Cherian, M.G., Jayasurya, A. and Bay, B.H. (2003) the road ahead. Cell 104, 503.
Metallothioneins in human tumors and potential
52. Wang, H., Nair, M.G. and Strasburg, G.M. (1999)
roles in carcinogenesis. Mutat. Res.10, 201.
Antioxidant and antiinflammatory activities of
43. Ozgocmen, S., Kaya, H. and Fadillioglu, E. (2007) anthocyanins and their aglycon, cyanidin, from tart
Role of antioxidant systems, lipid peroxidation, cherries. J. Natur. Produc. 62, 802.
and nitric oxide in postmenopausal osteoporosis.
Molecular and Cellular Biochemistry. 295, 45.
Prof. Sang Sun Lee
44. Madhujith, T. and Shahidi, F. (2005) Antioxidant
potential of pea beans (Phaseolus vulgaris L.). J. Department of Food & Nutrition
Food Sci. 70, 85. Hanyang University,
#17 Haengdang-dong
45. Wang, D., Wang, L.J., Zhu, E.X., Zhu, J.Y., Chen, Seongdong-gu
X.D., Zou, L., Saito, M. and Li, L.T. (2008) In vitro Seoul 133 – 791
and in vivo studies on the antioxidant activities of the South Korea
aqueous extracts of Douchi (a traditional Chinese Telephone: +82–2-2220–1206
salt-fermented soybean food). Food Chem. 107, Fax: +82–2-2281–8285
1421. E-mail: leess@hanyang.ac.kr
Int. J. Vitam. Nutr. Res., 80 (2), 2010, © Hogrefe & Huber Publishers
All in-text references underlined in blue are linked to publications on ResearchGate, letting you access and read them immediately.