References
- Neugarten BL, Kraines RJ. "Menopausal symptoms" in women of various ages. Psychosom Med. 1965 ; 27 : 266-73. https://doi.org/10.1097/00006842-196505000-00009
- Grady D. Management of menopausal symptoms. N Engl J Med. 2006 ; 355 : 2338-47. https://doi.org/10.1056/NEJMcp054015
- Cho HS, Kim HG, Ahn S, Yoo GN. A case report of the effects of Jia Wei Si Wu Tang (augmented four-substance decoction) on a menopausal disorder patient. J Korea Instit Orient Med Diagn. 2011 ; 15(2) : 215-222
- Du HK. Oriental kidney system internal medicine. Seoul:Sungbosa. 2003 : 1241-50.
- Rossouw JE, Anderson GL, Prentice RL, LaCroix AZ, Kooperberg C, Stefanick ML, Jackson RD, Beresford SAA, Howard BV, Johnson KC, Kotchen JM, Ockene J. Risks and benefits of estrogen plus progestin in healthy postmenopausal women : principal results from the women's health initiative randomized controlled trial. JAMA. 2002 ; 288 : 321-33. https://doi.org/10.1001/jama.288.3.321
- Lobo RA. Benefits and risks of estrogen replacement therapy. Am J Obstet Gynecol. 1995 ; 173 : 982-9. https://doi.org/10.1016/0002-9378(95)90247-3
- Wallach EE, Gambrell Jr RD. The menopause benefits and risks of estrogen - progestogen replacement therapy. Fertil Steril. 1982 ; 37 : 457-74. https://doi.org/10.1016/S0015-0282(16)46149-2
- Kronenberg F, Fugh-Berman A. Complementary and alternative medicine for menopausal symptoms : a review of randomized, controlled trials. Ann Intern Med. 2002 ; 137 : 805-13. https://doi.org/10.7326/0003-4819-137-10-200211190-00009
- Han KK, Soares Jr JM, Haidar MA, De Lima GR, Baracat EC. Benefits of soy isoflavone therapeutic regimen on menopausal symptoms. Obstet Gynecol. 2002 ; 99 : 389-94.
- Chung MH, Kim GW, Lee BJ, Um KJ. Studies on efficacy of Polygoni multiflori Radix and Cynanchi wilfordi Radix. Kor. J. Pharmacogn. 1991 ; 22(1) : 67.
- Kim HJ. Effects of Cynanchum wilfordii extract on serum lipid components and enzyme activities in hyperlipidemic and streptozotocin induced diabetic rats. Korean J. Human. Ecology. 2004 ; 7(2) : 1-11.
- Kim HK, Kim YA, Lee AY, Ko BS. Pattern analysis of Cynanchi wilfordii radix and Polygoni multiflori radix. Kor J Pharmacogn. 2003 ; 34(4) : 278-81
- Qiu S, Cho JS, Kim JT, Moon JH, Zhou Y, Lee SB, Park HJ, Lee HJ. Caudatin suppresses adipogenesis in 3T3-L1 adipocytes and reduces body weight gain in high-fat diet-fed mice through activation of hedgehog signaling. Phytomedicine. 2021 ; 92 : 153715 https://doi.org/10.1016/j.phymed.2021.153715
- Wang LJ, Chen H, Ma YB, Huang XY, Geng CA, Zhang XM, Chen JJ. Design, synthesis and biological evaluation of caudatin analogs as potent hepatitis B virus inhibitors. Med Chem. 2015 ; 11(2) : 165-79. https://doi.org/10.2174/1573406410666140902111326
- Zhen X, Choi HS, Kim JH, Kim SL, Liu R, Ko YC, Yun BS, Lee DS. Caudatin isolated from Cynanchumauriculatum inhibits breast cancer stem cell formation via a GR/YAP Signaling. Biomolecules. 2020 18 ; 10(6) : 925. https://doi.org/10.3390/biom10060925
- Song J, Ding W, Liu B, Liu D, Xia Z, Zhang L, Cui L, Luo Y, Jia X, Feng L. Anticancer effect of caudatin in diethylnitrosamine-induced hepatocarcinogenesis in rats. Mol Med Rep. 2020 ; 22(2) : 697-706. https://doi.org/10.3892/mmr.2020.11135
- 한국한의학연구원. 비주화(啤酒花) [Internet]. 특허청; 2007. Available from: https://doi.org/10.20929/KTKP.MED.0000078189
- Cleemput MV, Cattoor K, Bosscher KD, Haegeman G, Keukeleire DD, Heyerick A. Hop (Humulus lupulus)-derived bitter acids as multipotent bioactive compounds. J. Nat. Prod. 2009 ; 72 : 1220-1230. https://doi.org/10.1021/np800740m
- Wang J, Li D, Dangott LJ, Wu G. Proteomics and Its Role in Nutrition Research. The Journal of Nutrition. 2006 ; 136(7) : 1862-1867. https://doi.org/10.1093/jn/136.7.1862
- Effenberger KE, Johnsen SA, Monroe DG, Spelsberg TC, Westendorf JJ. Regulation of osteoblastic phenotype and gene expression by hop-derived phytoestrogens. J Steroid Biochem Mol Biol. 2005 ; 96 : 387-99. https://doi.org/10.1016/j.jsbmb.2005.04.038
- Humpel M, Isaksson P, Schaefer O, Kaufmanna U, Ciana P, Maggic A, Schleuning WD. Tissue specificity of 8-prenylnaringenin: protection from ovariectomy induced bone loss with minimal trophic effects on the uterus. J Steroid Biochem Mol Biol. 2005 ; 97 : 299-305. https://doi.org/10.1016/j.jsbmb.2005.05.009
- Diel P, Thomae RB, Caldarelli A, Zierau O, Kolba S, Schmidt S, Schwab P, Metz P, Vollmer G. Regulation of gene expression by 8-prenylnaringenin in uterus and liver of Wistar rats. Planta Med. 2004 ; 70 : 39-44. https://doi.org/10.1055/s-2004-815453
- Pepper MS, Hazel SJ, Humpel M, Schleuning WD. 8-Prenylnaringenin, a novel phytoestrogen, inhibits angiogenesis in vitro and in vivo. J Cell Physiol. 2004 ; 199 : 98-107. https://doi.org/10.1002/jcp.10460
- Zierau O, Morrissey C, Watson RWG, Schwab P, Kolba S, Metz P, Vollmer G. Antiandrogenic activity of the phytoestrogens naringenin, 6-(1,1-dimethylallyl) naringenin and 8-prenylnaringenin. Planta Med. 2003 ; 69 : 856-8 https://doi.org/10.1055/s-2003-43222
- Sathyamoorthy N, Wang TTY, Phang JM. Stimulation of pS2 expression by diet-derived compounds. Cancer Res. 1994 ; 54 : 957-61.
- Loven MA, Wood JR, Nardulli AM. Interaction of estrogen receptors α and β with estrogen response elements. Mol Cell Endocrinol. 2001 ; 181 : 151-63. https://doi.org/10.1016/S0303-7207(01)00491-9
- Lindsay R. The menopause and osteoporosis. Obstet Gynecol. 1996 ; 87 : 16S-9S. https://doi.org/10.1016/0029-7844(95)00430-0
- Oursler MJ. Direct and indirect effects of estrogen on osteoclasts. J Musculoskelet Neuronal Interact. 2003 ; 3 : 363-6.
- Nishikawa M, Akatsu T, Katayama Y, Yasutomo Y, Kado S, Kugal N, Yamamoto M, Nagata N. Bisphosphonates act on osteoblastic cells and inhibit osteoclast formation in mouse marrow cultures. Bone. 1996 ; 18 : 9-14. https://doi.org/10.1016/8756-3282(95)00426-2
- Abrahamsen B. Bisphosphonate adverse effects, lessons from large databases. Curr Opin Rheumatol. 2010 ; 22(4) : 404-9. https://doi.org/10.1097/BOR.0b013e32833ad677
- Silverman SL, Lane NE. Glucocorticoid-induced osteoporosis. Curr Osteoporos Rep. 2009 ; 7(1) : 23-6. https://doi.org/10.1007/s11914-009-0005-4
- Cho SI. Effects of the Rehmanniae radix preparat on ovariectomized rats. Kor J Herbology. 2005 ; 20(4) : 61-7.
- Kim JH, Kim JY, Ann JY, Park HJ, Kim HJ, Kwak HB, Oh JM, Kim YK. Inhibitory effects of Achyranthis bidentatae radix on osteoclast differentiation and bone resorption. Kor J Herbology. 2010 ; 25(1) : 65-74.
- Hwang JS, Seo BI, Park JH, Roh SS, Kim MY, KimSM, Goo JS. Effect of Cervi cornu on treatment of osteoporosis in ovariectomized rats. Kor J Herbology. 2010 ; 25(2) : 1-10.
- Velarde MC. Pleiotropic actions of estrogen: a mitochondrial matter. Physiological Genomics. 2013 ; 45(3) : 106-9. https://doi.org/10.1152/physiolgenomics.00155.2012
- Hu P, Kinyamu HK, Wang L, Martin J, Archer TK, Teng C. Estrogen induces estrogen-related receptor alpha gene expression and chromatin structural changes in estrogen receptor (ER)-positive and ER-negative breast cancer cells. J Biol Chem. 2008 ; 283(11) : 6752-63. https://doi.org/10.1074/jbc.M705937200
- Lee E, Jang M, Lima TG, Kim T, Ha H, Lee JH, Hong HD, Cho CW. Selective activation of the estrogen receptor-β by the polysaccharide from Cynanchum wilfordii alleviates menopausal syndrome in ovariectomized mice. Int J Biol Macromol. 2020 ; 165(Pt A) : 1029-37. https://doi.org/10.1016/j.ijbiomac.2020.09.165
- Rasmussen TH, Nielsen, JB. Critical parameters in the MCF-7 cell proliferation bioassay (E-Screen). Biomarkers. 2002 ; 7(4) : 322-36. https://doi.org/10.1080/13547500210132907