참고문헌
- J. Cell Biochem. v.22 Rationale for the use of genistein-containing soy matrices in chemoprevention trials for breast and prostate cancer Barnes, S.;Peterson, T.G.;Coward, L.
- Drug Saf. v.24 Risks and benefits of soy phytoestrogens in cardiovascular diseases, cancer, climacteric symptoms and osteoporosis Sirtori, C.R. https://doi.org/10.2165/00002018-200124090-00003
- Acta. Paediatr. Suppl. v.402 Nutritional aspects of soy formula Lonnerdal, B.
- J. Nutr. v.133 Cancer inhibition by inositol hexaphosphate (IP6) and inositol: from laboratory to clinic Vucenik, I.;Shamsuddin, A.M. https://doi.org/10.1093/jn/133.11.3778S
- Am. J. Clin. Nutr. v.76 A single daily dose of soybean phytosterols in ground beef decreases serum total cholesterol and LDL cholesterol in young, mildly hypercholesterolemic men Matvienko, O.A.;Lewis, D.S.;Swanson, M.;Arndt, B.;Rainwater, D.L.;Stewart, J.;Alekel, D.L.
- J. Nutr. v.116 Influence of saponins on gut permeability and active nutrient transport in vitro Johnson, I.T.;Gee, J.M.;Price, K.;Curl, C.;Fenwick, G.R. https://doi.org/10.1093/jn/116.11.2270
- J. Nutr. v.131 Soy protein, saponins and plasma cholesterol Oakenfull, D.
- J. Nutr. v.125 Saponins as anticarcinogens Rao, A.V.;Sung, M.K.
- Justus Liebigs Ann. Chem. v.489 Isoflavon- und saponin-glucoside in Soja-Hispida Walz, E. https://doi.org/10.1002/jlac.19314890110
- J. Am. Oil Chem. Soc. v.63 Genistin (an isoflavone glucoside) and its aglucone, genistein, from soybeans Walter, E.D. https://doi.org/10.1021/ja01857a013
- Phytochemistry v.12 A new isoflavone from soya beans Naim, M.;Gestetner, B.;Kirson, I.;Birk, Y.;Bondi, A. https://doi.org/10.1016/S0031-9422(00)84641-5
- Agric. Biol. Chem. v.55 Malonyl isoflavone glycosides in soybean seeds (Glycine Max merrill) Kudou, S.;Fleury, Y.;Welti, D. https://doi.org/10.1271/bbb1961.55.2227
- Mammalian lignans and phyto-oestrogens: recent studies on their formation metabolism and biological role in health and disease;Role of the Gut Flora in Toxicity and Cancer Setchell, K.D.R.;Adlercreutz, H.;Rowland, I.R.(ed.)
- Biochim. Biophys. Acta v.560 Physiological and pharmacological effects of estrogens in breast cancer Leclerq, G.;Heuson, J.C.
- Am. J. Clin. Nutr. v.68 Soy isoflavone analysis: quality control and a new internal standard Song, T.;Barua, K.;Buseman, G.;Murphy, P.A. https://doi.org/10.1093/ajcn/68.6.1474S
- Korean J. Food Sci. Technol. v.34 Determination of isoflavone, total saponin, dietary fiber, soy oligosaccharides and lecithins from commercial soy products based on the one serving size Kim, C.H.;Park, J.S.;Sohn, H.S.;Chung, C.W.
- J. Nutr. v.125 In vitro hormonal effects of soybean isoflavones Molteni, A.;Brizio-Molteni, L.;Persky, V.
- J. Endocrinol. v.37 Steroid and phytoestrogen binding to sheep uterine receptors in vitro Shutt, D.A.;Cox, R.I.
- J. Natl. Cancer Inst. v.64 Affinity of phytoestrogen for estradiol-binding proteins and effects of coumestrol on growth of 7,12-dimethylbenz(a)anthracene-induced rat mammary tumors Verdeal, K.;Brown, R.R.;Richardson, T.;Ryan, D.S.
- J. Endocrinol. v.85 Effect of equol on oestrogen receptors and on synthesis of DNA and protein in the immature rat uterus Tang, B.Y.;Adams, N.R. https://doi.org/10.1677/joe.0.0850291
- Proc. Natl. Acad. Sci. USA v.93 Cloning of a novel estrogen receptor expressed in rat prostate and ovary Kuiper, G.G.J.M.;Enmark, E.;Pelto-Huikko, M.;Nilsson, S.;Gustafsson, J.A.
-
Endocrinology (Baltimore)
v.138
Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors
${\alpha}\; and\;{\beta}$ Kuiper, G.G.J.M.;Carlsson, B.;Grandien, K. https://doi.org/10.1210/en.138.3.863 -
Biochem. Biophys. Res Commun.
v.248
Identification of estrogen receptor
${\beta}$ RNA in human breast and abdominal subcutaneous adipose tissue Crandall, D.L.;Busler, D.E.;Novak, T.J.;Weber, R.V.;Kral, J.G. https://doi.org/10.1006/bbrc.1998.8997 -
Endocrinology (Baltimore)
v.138
Differential expression of estrogen receptors
${\alpha}\;and\;{\beta}$ mRNA during differentiation of human osteoblast SV-HFO cells Arts, J.;Kuiper, G.G.J.M.;Janssen, J.M.M.F. https://doi.org/10.1210/en.138.11.5067 -
Proc. Natl. Acad. Sci. USA
v.96
Differentiation between vasculoprotective and uterotrophic effects of ligands with different binding affinities to estrogen receptors
${\alpha}\;and\;{\beta}$ Makela, S.;Savolainen, H.;Aavik, E.;Myllarniemi, M.;Strauss, L.;Taskinen, E.;Gustafsson, J.A.;Hayry, P. -
J. Biol. Chem.
v.276
Estrogen receptor
${\beta}-selective$ transcriptional activity and recruitment of coregulators by phytoestrogens Tzagarakis-Foster, C.A.Z.;Scharschmidt, T.C.;Lomri, N.;Leitman, D.C. https://doi.org/10.1074/jbc.M100953200 - Lancet v.350 Case control study of phytoestrogens and breast cancer Ingram, D.;Sanders, K.;Kolybaba, M.;Lopez, D. https://doi.org/10.1016/S0140-6736(97)01339-1
- Menopause v.7 Phytoestrogen and breast cancer in postmenopausal women: a case control study Murkies, A.;Dalais, F.S.;Briganti, E.M.;Burger, H.G.;Healy, D.L.;Wahlqvist, M.L.;Davis, S.R. https://doi.org/10.1097/00042192-200007050-00003
- Anticancer Res. v.16 Inhibition of N-methyl-N-nitrosourea-induced mammary tumors in mts by the soybean isoflavones Constantinou, A.I.;Mehta, R.G.;Vaughan, A.
- Carcinogenesis v.21 Inhibitory effects of bifidobacterium-fermented soy milk on 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine-induced rat mammary carcinogenesis, with a partial contribution of its component isoflavones Ohta, T.;Nakatsugi, S.;Watanabe, K.;Kawamori, T.;Ishikawa, F.;Morotomi, M.;Sugie, S.;Toda, T.;Sugimura, T.;Wakabayashi, K. https://doi.org/10.1093/carcin/21.5.937
- Anticancer Res. v.20 Antitumor effects of soybean hypocotyls and soybeans on the mammary tumor induction by N-methyl-N-nitrosourea in F344 rats Zaizen, Y.;Higuchi, Y.;Matsuo, N.;Shirabe, K.;Tokuda, H.;Takeshita, M.
- Cancer Res. v.49 Prospective study of demographics, diet, and prostate cancer among men of Japanese ancestry in Hawaii Severson, R.K.;Nomura, A.M.;Grove, J.S.;Stemmermann, G.N.;Stemmermann, A.
- J. Natl. Cancer Inst. v.90 Nutritional and socioeconomic factors in relation to prostate cancer mortality: a crosssnational study Hebert, J.R.;Hurley, T.G.;Olendzki, B.C.;Teas, J.;Ma, Y.;Hampl, J.S. https://doi.org/10.1093/jnci/90.21.1637
- Nutr. Cancer v.35 Decreased growth of human prostate LNCaP tumors in SCID mice fed a low-fat, soy protein diet with isoflavones Aronson, W.J.;Tymchuk, C.N.;Elashoff, R.M.;McBride, W.H.;McLean, C.;Wang, H.;Heber, D. https://doi.org/10.1207/S15327914NC352_6
- Prostate v.42 Rye bran and soy protein delay growth and increase apoptosis of human LNCaP prostate adenocarcinoma in nude mice Bylund, A.;Zhang, J.X.;Bergh, A.;Damber, J.E.;Widmark, A.;Johansson, A.;Adlercreutz, H.;Aman, P.;Shepherd, M.J.;Hallmans, G. https://doi.org/10.1002/(SICI)1097-0045(20000301)42:4<304::AID-PROS8>3.0.CO;2-Z
- Int. J. Oncol. v.16 Inhibition of prostate-specific antigen expression by genistein in prostate cancer cells Davis, J.N.;Muqim, N.;Bhuiyan, M.;Kucuk, O.;Pienta, K.J.;Sarkar, F.H.
- Cancer Res. v.61 Genistein in the diet reduces the incidence of poorly differentiated prostatic adenocarcinoma in transgenic mice (TRAMP) Mentor-Marcel, R.;Lamartiniere, C.A.;Eltoum, I.E.;Greenberg, N.M.;Elgavish, A.
- Mol. Cell. Endocrinol. v.186 Dietary genistein down-regulates androgen and estrogen receptor expression in the rat prostate Fritz, W.A.;Wang, J.;Eltoum, I.E. https://doi.org/10.1016/S0303-7207(01)00663-3
- Proc. Soc. Exp. Biol. Med. v.208 Estrogenic flavonoids: structural requirements for biological activity Miksicek, R.J.
- Endocrinology v.139 Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor beta Kuiper, G.G.;Lemmen, J.G.;Carlsson, B.;Corton, J.C.;Safe, S.H.;Van der Saag, P.T.;Van der Burg, B.;Gustafsson, J.A. https://doi.org/10.1210/en.139.10.4252
- Proc. Natl. Acad. Sci. U.S.A. v.90 Genistein, a dietary-derived inhibitor of in vitro angiogenesis Fotsis, T.;Pepper, M.;Adlercreutz, H.;Fleischmann, G.;Hase, T.;Montesano, R.;Schweigerer, L.
- Ann. Med. v.29 Phyto-oestrogens and western diseases Adlercreutz, H.;Mazur, W. https://doi.org/10.3109/07853899709113696
- J. Endocrinol. v.147 Inhibition of 5 a-reductase in genital skin fibroblasts and prostate tissue by dietary lignans and isoflavonoids Evans, B.A.J.;Griffiths, K.;Morton, M.S. https://doi.org/10.1677/joe.0.1470295
-
Proc. Soc. Exp. Biol. Med.
v.217
Inhibition of
$17{\beta}-hydroxysteroid$ oxidoreductase by flavonoids in breast and prostate cancer cells Makela, S.;Poutanen, M.;Kostian, M.L.;Lehtimaki, N.;Strauss, L.;Santti, R.;Vihko, R. - J. Steroid Biochem. Mol. Biol. v.44 Inhibition of human aromatase by mammalian lignans and isoflavonoid phytoestrogens Adlercreutz, H.;Bannwart, C.;Wahala, K.;Makela, T.;Brunow, G.;Hase, T.;Arosemena, P.J.;Kellis, J.T. Jr.;Vickery, L.E. https://doi.org/10.1016/0960-0760(93)90022-O
- Br. J. Cancer. v.75 Inhibition of growth and induction of differentiation of metastatic melanoma cells in vitro by genistein: chemosensitivity is regulated by cellular p53 Rauth, S.;Kichina, J.;Green, A. https://doi.org/10.1038/bjc.1997.268
- J. Nutr. v.126 Soybean isoflavones improve cardiovascular risk factors without affecting the reproductive system in prepubertal monkeys Anthony, M.S.;Clarkson, T.B.;Hughes, C.L. Jr.;Morgan, T.M.;Burke, G.L. https://doi.org/10.1093/jn/126.1.43
- Arch. Intern. Med. v.159 A randomized trial comparing the effects of casein with that of soy protein containing varying amounts of isoflavones on plasma concentrations of lipids and lipoproteins Crouse, J.R. III;Morgan, T.;Terry, J.G.;Ellis, J.;Vitolins, M.;Burke, G.L. https://doi.org/10.1001/archinte.159.17.2070
- J. Nutr. v.128 Supplementation with isoflavonoid phytoestrogens does not alter serum lipid concentrations: a randomized controlled trial in humans Hodgson, J.M.;Puddey, I.B.;Beilin, L.J.;Mori, T.A.;Croft, K.D.
- J. Nutr. v.126 A soy protein isolate rich in genistein and daidzein and its effects on plasma isoflavone concentration, platelet aggregation, blood lipids and fatty acid composition of plasma phospholipid in normal men Gooderham, M.J.;Adlercreutz, H.;Ojala, S.T.;Wahala, K.;Holub, B.J.
- Am. J. Cardiol. v.85 Phytoestrogens do not influence lipoprotein levels or endothelial function in healthy, postmenopausal women Simons, L.A.;von Konigsmark, M.;Simons, J.;Celermajer, D.S. https://doi.org/10.1016/S0002-9149(00)00759-1
- N. Engl. J. Med. v.333 Meta-analysis of the effects of soy protein intake on serum lipids Anderson, J.W.;Johnstone, B.M.;Cook-Newell, M.E. https://doi.org/10.1056/NEJM199508033330502
- 21 CFR Part 101 Fed.Regist. v.64 Food labeling:health claims:soy protein and coronary heart disease Food and Drug Administration
- J. Nutr. v.129 Intact dietary soy protein, but not adding an isoflavone-rich soy extract to casein,improves plama lipids in ovariectomized cynomologus monkeys Greaves, K.A.;Parks, J.S.;Williams, J.K.;Wagner, J.D. https://doi.org/10.1093/jn/129.8.1585
- Biochem. Biophys. Res. Commun. v.258 Genistein is neuroprotective in murine models of familial amyotrophic lateral sclerosis and stroke Trieu, V.N.;Uckun, F.M. https://doi.org/10.1006/bbrc.1999.0577
- Br. J. Pharmacol. v.128 Cardioprotection by the phytoestrogen genistein in experimental ischaemia-reperfusion injury Deodato, B.;Altavilla, D.;Squadrito, G.;Campo, G.M.;Arlotta, M.;Minutoli, L.;Saitta, A.;Cucinotta, D.;Calapai, G.;Caputi, A.P.;Miano, M.;Squadrito, F. https://doi.org/10.1038/sj.bjp.0702973
- Proc. Natl. Acad. Sci. USA v.95 Effects of phytoestrogen intake on low density lipoprotein oxidation resistance Tikkanen, M.J.;Wahala, K.;Ojala, S.;Vihma, V.;Adlercreutz, H.
- Metabolism v.49 Effects of soy protein food on low density lipoprotein oxidation and ex vivo sex hormone receptor activity-a controlled cross over trial Jenkins, D.J.A.;Kendall, C.W.C.;Garsetti, M.;Rosenberg-Zand, R.S.;Jackson, C.J.;Agarwal, S.;Rao, A.V.;Diamandis, E.P.;Parker, T.;Faulkner, D.;Vuksan, V.;Vidgen, E. https://doi.org/10.1016/S0026-0495(00)80022-0
- Thromb.Vasco Biol. v.17 Soy protein versus soy phytoestrogens in the prevention of diet-induced coronary artery atherosclerosis of male cynomolgus monkeys Anthony, M.S.;Clarkson, T.B.;Bullock, B.C.;Wagner, J.D. https://doi.org/10.1161/01.ATV.17.11.2524
- Fertil. Steril. v.67 Soy isoflavones enhance coronary vascular reactivity in atherosclerotic female macaques Honore, E.K.;Williams, J.K.;Anthony, M.S.;Clarkson, T.B. https://doi.org/10.1016/S0015-0282(97)81872-9
-
FEBS Lett.
v.315
The tyrosine kinase inhibitors methyl 2,5-dihydroxycinnamate and genistein reduce thrombin-evoked tyrosine phosphorylation and
$Ca^{2+}$ entry in human platelets Sargeant, P.;Farndale, R.W.;Sage, S.O. https://doi.org/10.1016/0014-5793(93)81172-V - Arterioscler.Thromb.Vasco Biol. v.17 Soy isoflavones improve systemic arterial compliance but not plasma lipids in menopausal and perimenopausal women Nestel, P.J.;Yamashita, T.;Sasahara, T.;Pomeroy, S.;Dart, A.;Komesaroff, P.;Owen, A.;Abbey, M. https://doi.org/10.1161/01.ATV.17.12.3392
- Am. J. Clin. Nutr. v.76 Effects of high-and low-isoflavone soyfoods on blood lipids,oxidized LDL, homocysteine,and blood pressure in hyperlipidemic men and women Jenkins, D.J.;Kendall, C.W.;Jackson, C.J.;Connelly, P.W.;Parker, T.;Faulkner, D.;Vidgen, E.;Cunnane, S.C.;Leiter, L.A.;Josse, R.G.
- Am. J. Epidemiol. v.144 Prevalence of dementia and its subtypes in the Japanese American population of King County, Washington state :The Kame Project Graves, A.B.;Larson, E.B.;Edland, S.D.;Bowen, J.D.;McCormick, W.C.;McCurry, S.M.;Rice, M.M.;Wenzlow, A.;Uomoto, J.M. https://doi.org/10.1093/oxfordjournals.aje.a009000
- Neurosci. Lett. v.261 Evidence for up-regulation of brain-derived neurotrophic factor mRNA by soy phytoestrogens in the frontal cortex of retired breeder female rats Pan, Y.;Anthony, M.;Clarkson, T.B. https://doi.org/10.1016/S0304-3940(98)00994-X
- Proc. Soc. Exp. Biol. Med. v.221 Effect of estradiol and soy phytoestrogens on choline acetyltransferase and nerve growth factor mRNAs in the frontal cortex and hippocampus of female rats Pan, Y.;Anthony, M.;Clarkson, T.B.
-
Menopause
v.7
Soy phytoestrogens improve radial arm maze performance in ovariectomized retired breeder rats and do not attenuate benefits of
$17{\beta}-estradiol$ treatment Pan, Y.;Anthony, M.;Watson, S.;Clarkson, T.B. https://doi.org/10.1097/00042192-200007040-00004 - BMC Neuroscience v.2 Visual spatial memory is enhanced in females (but not in males)by dietary soy phytoestrogens Lund, T.D.;West, T.W.;Tian, L.Y.;Bu, L.H.;Simmons, D.L.;Setchell, K.D.;Adlercreutz, H.;Lephart, E.D. https://doi.org/10.1186/1471-2202-2-20
- J. Am. Coll. Nutr. v.19 Brain aging and midlife tofu consumption White, L.R.;Petrovitch, H.;Ross, G.W.;Masaki, K.;Hardman, J.;Nelson, J.;Davis, D.;Markesbery, W.
- Brain Res. v.913 Dietary soy phytoestrogens produce anxiolytic effects in the elevated plusmaze Lund, T.D.;Lephart, E.D. https://doi.org/10.1016/S0006-8993(01)02793-7
- Brain Res. v.120 Pre-or postnatal testosterone and flutamide effects on sexually dimorphic nuclei of the rat hypothalamus Lund, T.D.;Salyer, D.L.;Fleming, D.E.;Lephart, E.D. https://doi.org/10.1016/S0165-3806(00)00013-4
- Neurotoxicol Teratol. v.24 Neurobehavioral effects of dietary soy phytoestrogens Lephart, E.D.;West, T.W.;Weber, K.S.;Rhees, R.W.;Setchell, K.D.;Adlercreutz, H.;Lund, T.D. https://doi.org/10.1016/S0892-0362(01)00197-0
- Psychopharmacology v.157 Soya improves human memory File, S.E.;Jarrett, N.;Fluck, E.;Duffy, R.;Casey, K.;Wiseman, H. https://doi.org/10.1007/s002130100845
- Ann. NY. Acad. Sci. v.933 Plasticity of the hippocampus:adaptation to chronic stress and allostatic load McEwen, B.S. https://doi.org/10.1111/j.1749-6632.2001.tb05830.x
- Brain Res. v.467 Developmental change in the nerve growth factor action from induction of choline acetyltransferase to promotion of cell survival in cultured basal forebrain cholinergic neurons from postnatal rats Hatanaka, H.;Tsukui, H.;Nihonmatsu, I.
- Neuroscience v.8 Development of septal cholinergic neurons in culture:plating density and glial cells modulate effects of NGF on survival,fiber growth,and expression of transmitter-specific enzymes Hartikka, J.;Hefti, F. https://doi.org/10.1523/JNEUROSCI.08-08-02967.1988
- Ann. Rev. Neurosci. v.22 Neurotrophins and synaptic plasticity McAllister, A.K.;Katz, L.C.;Lo, D.C. https://doi.org/10.1146/annurev.neuro.22.1.295
- Am. J. Epidemiol. v.155 Dietary soy isoflavones and bone mineral density: results from the study of women's health across the nation Greendale, G.A.;FitzGerald, G.;Huang, M.H.;Sternfeld, B.;Gold, E.;Seeman, T.;Sherman, S.;Sowers, M. https://doi.org/10.1093/aje/155.8.746
- Am. J. Clin. Nutr. v.68 Soy protein and isoflavones:their effects on blood lipids and bone density in postmenopausal women Potter, S.M.;Baum, J.A.;Teng, H.;Stillman, R.J.;Shay, N.F.;Erdman, J.W. https://doi.org/10.1093/ajcn/68.6.1375S
- Am. J. Clin. Nutr. v.72 Isoflavone-rich soy protein isolate attenuate bone loss in the lumbar spine of perimenopausal women Alekel, D.L.;Germain, A.;Peterson, C.T.;Hanson, K.B.;Stewart, J.W.;Toda, T.
- Biosci Biotechnol Biochem. v.68 Evaluation of the preventive effect of isoflavone extract on bone loss in ovariectomized rats Lee, Y.B.;Lee, H.J.;Kim, K.S.;Lee, J.Y.;Nam, S.Y.;Cheon, S.H.;Sohn, H.S. https://doi.org/10.1271/bbb.68.1040
- J.Cell BioChem. v.61 Variable effects of tyrosine kinase inhibitors on avian osteoclastic activity and reduction of bone loss in ovariectomized rats Blair, H.C.;Jordon, S.E.;Peterson, T.G.;Barnes, S. https://doi.org/10.1002/(SICI)1097-4644(19960616)61:4<629::AID-JCB17>3.0.CO;2-A
- Am. J. Clin. Nutr. v.68 Systemic administration of genistein partially prevents bone loss in ovariectomized rat in a nonestrogen-like mechanism Fanti, O.;Faugere, M.C.;Gang, Z.;Schmidt, J.;Cohen, D.;Malluche, H.H.
- J. Agric. Food Chem. v.50 Determination of saponins in legumes by direct densitometry Gurfinkel, D.M.;Rao, A.V. https://doi.org/10.1021/jf010754c
- Biosci. Biotechnol.Biochem. v.62 Relationship between chemical structures and biological activities of triterpenoid saponins from soybean Yoshiki, Y.;Kudou, S.;Okubo, K. https://doi.org/10.1271/bbb.62.2291
- Yakugaku Zasshi v.108 Saponin and sapogenol. XLIV. Soyasaponin composition in soybeans of various origins and soyasaponin content in various organs of soybean Taniyama, T.;Yoshikawa, M.;Kitagawa, I. https://doi.org/10.1248/yakushi1947.108.6_562
- Agric. Biol. Chem. v.55 Composition and content of saponins in soybean seed according to variety,cultivation year and maturity Shiraiwa, M.;Harada, K.;Okubo, K. https://doi.org/10.1271/bbb1961.55.911
- Agric. Biol. Chem. v.54 Distributions of saponin constituents in some varieties of soybean plant Shimoyamada, M.;Kudo, S.;Okubo, K.;Yamauchi, F.;Harada, K. https://doi.org/10.1271/bbb1961.54.77
- J. Sci. Food Agric v.37 Saponin content of soya and some commercial soya products by means of high-performance liquid chromatography of the sapogenins Ireland, P.A.;Dziedzic, S.Z.;Kearsley, M.W. https://doi.org/10.1002/jsfa.2740370715
- Yakugaku Zasshi v.104 Quantitative determination of soyasaponin in soybeans of various origins and soybean products by means of high performance liquid chromatography Kitagawa, I.;Yoshikawa, M.;Hayashi, T.;Taniyama, T.
- Fed. Proc. v.33 Ultrastructure of membrane lesions in immune lysis, smotic lysis and drug-induced lysis Seeman, P.
- Br. J. Nutr. v.55 A mechanism for the hypocholesterolaemic activity of saponins Sidhu, G.S.;Oakenfull, D.G. https://doi.org/10.1079/BJN19860070
- Planta Med. v.50 Effects of soyasaponins on liver injury induced by highly peroxidized fat in rats Ohminami, H.;Kimura, Y.;Okuda, H.;Arichi, S.;Yoshikawa, M.;Kitagawa, I. https://doi.org/10.1055/s-2007-969760
-
Planta Med.
v.64
Kaikasaponin III and soyasaponin I, major triter- pene saponins of Abrus cantoniensis, act on GOT and GPT: influence on transaminase elevation of rat liver cells concomitantly exposed to
$CCl_4$ for one hour Miyao, H.;Arao, T.;Udayama, M.;Kinjo, J.;Nohara, T. https://doi.org/10.1055/s-2006-957355 - Planta Med. v.64 Structure-hepatoprotective relationships study of soyasaponins I-IV having soyasapogenol B as aglycone Kinjo, J.;Imagire, M.;Udayama, M.;Arao, T.;Nohara, T. https://doi.org/10.1055/s-2006-957416
- Nutr. Cancer v.23 Effect of soybean saponins and gypsophilla saponin on growth and viability of colon carcinoma cells in culture Sung, M.K.;Kendall, C.W.C.;Koo, M.M.;Rao, A.V. https://doi.org/10.1080/01635589509514380
- Nutr. Cancer v.27 Effect of soya bean saponins on azoxymethane-induced preneoplastic lesions in the colon of mice Koratkar, R.;Rao, A.V. https://doi.org/10.1080/01635589709514526
- J. Med. Food v.5 Protective effect of soybean saponins and major antioxidants against aflatoxin B1-induced mutagenicity and DNA-adduct formation Jun, H.S.;Kim, S.E.;Sung, M.K. https://doi.org/10.1089/109662002763003393
- Nutr. Cancer v.39 Soybean saponins inhibit cell proliferation by suppression PKC activation and induce differentiation of HT-29 human colon adenocarcinoma cells Oh, Y.J.;Sung, M.K. https://doi.org/10.1207/S15327914nc391_18
-
Cancer Lett.
v.210
Antiproliferative crude soy saponin extract modulates the expression of
$I{\kappa}B{\alpha}$ , protein kinase C, and cyclooxygenase-2 in human colon cancer cells Kim, H.Y.;Yu, R.;Kim, J.S.;Kim, Y.K.;Sung, M.K. https://doi.org/10.1016/j.canlet.2004.01.009 -
Biosci. Biotechnol.BioChem.
v.65
Superoxide-and 1,1-diphenyl-2-picryl- hydrazyl radical -scavenging activities of soyasaponin
${\beta}g$ related to gallic acid Yoshiki, Y.;Kahara, T.;Okubo, K.;Sakabe, T.;Yamasaki, T. https://doi.org/10.1271/bbb.65.2162 - Planta Med. v.62 Prevention of hydrogen peroxide damage by soybean saponins to mouse fibroblasts Yoshikoshi, M.;Yoshiki, Y.;Okubo, K.;Seto, J.;Sasaki, Y. https://doi.org/10.1055/s-2006-957871
- AIDS v.3 Inhibitory effect of glycosides like saponin from soybean on the infectivity of HIV in vitro Nakashima, H.;Okubo, K.;Honda, Y.;Tamura, T.;Matsuda, S.;Yamamoto, N. https://doi.org/10.1097/00002030-198910000-00007
-
Zhong Yao Cai
v.26
Study on the inhibition of
${\alpha}-glucosidase$ by soyasaponins Quan, J.;Yin, X.;Jin, M.;Shen, M.