DOI QR코드

DOI QR Code

Effect of dietary isoflavones of soybean by-product on estrogen and testosterone levels in mouse

  • Park, Sungkwon (Department of Food Science & Biotechnology, Sejong University) ;
  • Choi, Hojun (Department of Food Science & Biotechnology, Sejong University) ;
  • Seo, Jinyoun (BK21 plus Project Team, College of Pharmacy, Seoul National University) ;
  • Cho, Sangrae (BK21 plus Project Team, College of Pharmacy, Seoul National University) ;
  • Kim, Jungsang (School of Food Science and Biotechnology, Kyungpook National University) ;
  • Hong, Sung Wook (World Institute of Kimchi) ;
  • Park, Changseok (Yecheon Agriculture Technology Center)
  • Received : 2016.09.09
  • Accepted : 2016.11.29
  • Published : 2016.12.31

Abstract

Boar taint, an unpleasant odor of pork, is associated with two substances including androstenone and skatole. Testosterone is a steroid hormone as well as a strong predictor for androstenone secretion. Isoflavones of soy origin play a role in modulating the metabolism of sex hormones. Although several methods responsible for reducing boar taint are under investigation, the precise mechanism by which isoflavones reduce testosterone has not yet been identified. The objective of the current study was to investigate the effects of isoflavones extracted from a soy by-product on the concentration of serum testosterone in mouse. A total of 24 mice were supplemented with basal diet (control), daidzin plus genistin mix (T1), or isoflavone extracts (T2). After 11 days of treatment, size and weight of testis, as well as the concentration of sex hormones, including testosterone and estrogen, were analyzed. There was no difference in size or weight of testis from mice among control, T1, and T2. Serum testosterone levels were significantly decreased (p < 0.05) both in T1 and T2 when compared with the control group. Furthermore, estrogen concentration in blood was increased (p < 0.05) in T2 (numerically increased in T1) compared with the control group. Taken together, the use of isoflavones extracted from soy by-products would be a plausible strategy for reducing testosterone level, ultimately reducing boar taint without castration of piglets.

Keywords

References

  1. Akingbemi BT, Braden TD, Kemppainen BW, Hancock KD, Sherrill JD, Cook SJ, He X, Supko JG. 2007. Exposure to phytoestrogens in the perinatal period affects androgen secretion by testicular Leydig cells in the adult rat. Endocrinology 148:4475-4488. https://doi.org/10.1210/en.2007-0327
  2. Bateman HL, Patisaul HB. 2008. Disrupted female reproductive physiology following neonatal exposure to phytoestrogens or estrogen specific ligands is associated with decreased GnRH activation and kisspeptin fiber density in the hypothalamus. Neurotoxicology 29:988-997. https://doi.org/10.1016/j.neuro.2008.06.008
  3. Cederroth CR, Zimmermann C, Beny JL, Schaad O, Combepine C, Descombes P, Doerge DR, Pralong FP, Vassalli JD, Nef S. 2010. Potential detrimental effects of a phytoestrogen-rich diet on male fertility in mice. Molecular and Cellular Endocrinology 321:152-160. https://doi.org/10.1016/j.mce.2010.02.011
  4. Cimafranca MA, Davila J, Ekman GC, Andrews RN, Neese SL, Peretz J, Woodling KA, Helferich WG, Sarkar J, Flaws JA, Schantz SL, Doerge DR, Cooke PS. 2010. Acute and chronic effects of oral genistein administration in neonatal mice. Biology of Reproduction 83:114-121.
  5. Cline JM, Franke AA, Register TC, Golden DL, Adams MR. 2004. Effects of dietary isoflavone aglycones on the reproductive tract of male and female mice. Toxicologic Pathology 32:91-99. https://doi.org/10.1080/01926230490265902
  6. Dillingham BL, McVeigh BL, Lampe JW, Duncan AM. 2005. Soy protein isolates of varying isoflavone content exert minor effects on serum reproductive hormones in healthy young men. Journal of Nutrition 135:584-591. https://doi.org/10.1093/jn/135.3.584
  7. Dupont S, Krust A, Gansmuller A, Dierich A, Chambon P, Mark M. 2000. Effect of single and compound knockouts of estrogen receptors alpha (ERalpha) and beta (ERbeta) on mouse reproductive phenotypes. Development 127:4277-4291.
  8. Glover A, Assinder SJ. 2006. Acute exposure of adult male rats to dietary phytoestrogens reduces fecundity and alters epididymal steroid hormone receptor expression. Journal of Endocrinology 189:565-573. https://doi.org/10.1677/joe.1.06709
  9. Goyal HO, Robateau A, Braden TD, Williams CS, Srivastava KK, Ali K. 2003. Neonatal estrogen exposure of male rats alters reproductive functions at adulthood. Biology of Reproduction 68:2081-2091. https://doi.org/10.1095/biolreprod.102.010637
  10. Hamilton-Reeves JM, Rebello SA, Thomas W, Slaton JW, Kurzer MS. 2007. Isoflavone-rich soy protein isolate suppresses androgen receptor expression without altering estrogen receptor-beta expression or serum hormonal profiles in men at high risk of prostate cancer. Journal of Nutrition 137:1769-1775. https://doi.org/10.1093/jn/137.7.1769
  11. Hancock KD, Coleman ES, Tao YX, Morrison EE, Braden TD, Kemppainen BW, Akingbemi BT. 2009. Genistein decreases androgen biosynthesis in rat Leydig cells by interference with luteinizing hormone-dependent signaling. Toxicology Letters 184:169-175. https://doi.org/10.1016/j.toxlet.2008.11.005
  12. Hu GX., Zhao BH, Chu YH, Zhou HY, Akingbemi BT, Zheng ZQ, Ge RS. 2010. Effects of genistein and equol on human and rat testicular 3beta-hydroxysteroid dehydrogenase and 17beta-hydroxysteroid dehydrogenase 3 activities. Asian Journal of Andrology 12:519-526. https://doi.org/10.1038/aja.2010.18
  13. Kamboh AA, Zhu WY. 2013. Effect of increasing levels of bioflavonoids in broiler feed on plasma anti-oxidative potential, lipid metabolites, and fatty acid composition of meat. Poultry Science 92:454-461. https://doi.org/10.3382/ps.2012-02584
  14. Kudou S, Shimoyamada M, Imura T, Uchida T, Okubo K. 1991. A new isoflavone glycoside in soybean seeds (Glycine max MERRILL), glycitein 7-O-${\beta}$-D-(6"-O-Acetyl) glucopyranoside. Agricultural and Biological Chemistry 55:859-860.
  15. Kuiper GG, Lemmen JG, Carlsson B, Corton JC, Safe SH, van der Saag PT, van der Burg B, Gustafsson JA. 1998a. Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor beta. Endocrinology 139:4252-4263. https://doi.org/10.1210/endo.139.10.6216
  16. Kuiper GG, Lemmen JG, Carlsson B, Corton JC, Safe SH, van der Saag PT, van der Burg B, Gustafsson JA. 1998b. Interaction of Estrogenic Chemicals and Phytoestrogens with Estrogen Receptor ${\beta}$. Endocrinology 139:4252-4263. https://doi.org/10.1210/endo.139.10.6216
  17. Mahmoud AM, Yang W, Bosland MC. 2014. Soy isoflavones and prostate cancer: a review of molecular mechanisms. The Journal of Steroid Biochemistry and Molecular Biology 140:116-132. https://doi.org/10.1016/j.jsbmb.2013.12.010
  18. McCarver G, Bhatia J, Chambers C, Clarke R, Etzel R, Foster W, Hoyer P, Leeder JS, Peters JM, Rissman E, Rybak M, Sherman C, Toppari J, Turner K. 2011. NTP-CERHR expert panel report on the developmental toxicity of soy infant formula. Birth Defects Research (Part B) 92:421-468. https://doi.org/10.1002/bdrb.20314
  19. Napier ID, Simon L, Perry D, Cooke PS, Stocco DM, Sepehr E, Doerge DR, Kemppainen BW, Morrison EE, Akingbemi BT. 2014. Testicular development in male rats is sensitive to a soy-based diet in the neonatal period. Biology of Reproduction 90:40.
  20. Rasmussen MK, Ekstrand B. 2014. Regulation of 3${\beta}$-hydroxysteroid dehydrogenase and sulphotransferase 2A1 gene expression in primary porcine hepatocytes by selected sex-steroids and plant secondary metabolites from chicory (Cichorium intybus L.) and wormwood (Artemisia sp.). Gene 536:53-58. https://doi.org/10.1016/j.gene.2013.11.092
  21. Sherrill JD, Sparks M, Dennis J, Mansour M, Kemppainen BW, Bartol FF, Morrison EE, Akingbemi BT. 2010. Developmental exposures of male rats to soy isoflavones impact Leydig cell differentiation. Biology of Reproduction 83:488-501.
  22. Thuillier R, Manku G, Wang Y, Culty M. 2009. Changes in MAPK pathway in neonatal and adult testis following fetal estrogen exposure and effects on rat testicular cells. Microscopy Research and Technique 72:773-786. https://doi.org/10.1002/jemt.20756
  23. Wang H, Murphy PA. 1994. Isoflavone composition of american and japanese soybeans in Iowa: Effects of variety, crop year, and location. Journal of Agricultural and Food Chemistry 42:1674-1677. https://doi.org/10.1021/jf00044a017
  24. Zamaratskaia G, Squires EJ. 2009. Biochemical, nutritional and genetic effects on boar taint in entire male pigs. Animal 3:1508-1521. https://doi.org/10.1017/S1751731108003674