Genistein increases progesterone secretion by elevating related enzymes in chicken granulosa cells

ABSTRACT Genistein, a biologically active isoflavone, exists in many soy products. It is well known that genistein binds to both oestrogen receptor alpha (ER&agr;) and oestrogen receptor beta (ER&bgr;), but it has a higher affinity to ER&bgr;. Genistein can also bind to the G protein‐coupled receptor 30 (GPR30, also known as G protein‐coupled oestrogen receptor 1 or GPER). Furthermore, weak oestrogenic activity has been found in genistein, but the mechanism of action remains unknown. The aim of this study was to investigate the in vitro effects of genistein on the secretion of progesterone (P4) and oestradiol (E2) in chicken granulosa cells harvested from follicles, as well as the mRNA expression of ERs in these cells. In addition, we examined the expression of key enzymes including steroidogenic acute regulatory protein (StAR), cytochrome P450 side‐chain cleavage (P450scc), and 3&bgr;‐hydroxysteroid dehydrogenase (3&bgr;‐HSD) in the process of P4 synthesis. The results showed that genistein did not affect the viability of granulosa cells, nor was the proliferating cell nuclear antigen (PCNA) protein changed. Among the 1‐, 10‐, 100‐, and 1,000‐nM concentrations tested, treatment with 1 nM genistein for 48 h significantly increased P4 but did not affect E2 secretion. Real‐time PCR results showed that the ER&bgr; gene expression in granulosa cells was markedly upregulated by 1 nM genistein treatment for 48 h, but there was no significant difference in ER&agr; and GPR30 expression. Genistein also increased the gene expression of StAR, P450scc and 3&bgr;‐HSD in the cultured granulosa cells. These results indicate that genistein acts directly on chicken granulosa cells to increase P4 production by upregulating the gene expression of key enzymes through binding in ER&bgr;. It may exert positive effects on the reproduction of late‐laying hens and act as an effective and safe feed additive for animals.

[1]  Yunqi Xiao,et al.  Comprehensive evaluation of the role of soy and isoflavone supplementation in humans and animals over the past two decades , 2018, Phytotherapy research : PTR.

[2]  S. Hu,et al.  Effects of nonglycosylated and glycosylated prolactin on basal and gonadotropin-stimulated steroidogenesis in chicken ovarian follicles. , 2017, Domestic animal endocrinology.

[3]  Dan Zhao,et al.  Effect of estrogen on chick primordial follicle development and activation , 2017, Cell biology international.

[4]  M. Messina Soy and Health Update: Evaluation of the Clinical and Epidemiologic Literature , 2016, Nutrients.

[5]  T. Minegishi,et al.  Retinoic acid enhances progesterone production via the cAMP/PKA signaling pathway in immature rat granulosa cells , 2016, Biochemistry and biophysics reports.

[6]  Sujith Ravi,et al.  Understanding genistein in cancer: The "good" and the "bad" effects: A review. , 2016, Food chemistry.

[7]  A. Sadowska,et al.  The Effects of Phytoestrogen Genistein on Steroidogenesis and Estrogen Receptor Expression in Porcine Granulosa Cells of Large Follicles. , 2015, Folia biologica.

[8]  H. Tong,et al.  Effects of High-Dose Daidzein on Laying Performance, Egg Quality and Antioxidation in Laying Hens , 2013 .

[9]  H. Tong,et al.  Safety evaluation of daidzein in laying hens: part II. Effects on calcium-related metabolism. , 2013, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[10]  H. Tong,et al.  Safety evaluation of daidzein in laying hens: part I. Effects on laying performance, clinical blood parameters, and organs development. , 2013, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[11]  B. Wąsowska,et al.  Effects of the phytoestrogen, genistein, and protein tyrosine kinase inhibitor-dependent mechanisms on steroidogenesis and estrogen receptor expression in porcine granulosa cells of medium follicles. , 2013, Domestic animal endocrinology.

[12]  R. Zhao,et al.  Effects of kisspeptin-10 on progesterone secretion in cultured chicken ovarian granulosa cells from preovulatory (F1–F3) follicles , 2011, Peptides.

[13]  F. Grasselli,et al.  The impact of the phyto-oestrogen genistein on swine granulosa cell function. , 2010, Journal of animal physiology and animal nutrition.

[14]  A. Nynca,et al.  Effects of phytoestrogen daidzein and estradiol on steroidogenesis and expression of estrogen receptors in porcine luteinized granulosa cells from large follicles. , 2009, Journal of physiology and pharmacology : an official journal of the Polish Physiological Society.

[15]  J. Vanselow,et al.  In vitro exposure of porcine granulosa cells to the phytoestrogens genistein and daidzein: effects on the biosynthesis of reproductive steroid hormones. , 2007, Reproductive toxicology.

[16]  M. Beck,et al.  Activity of three-beta-hydroxysteroid dehydrogenase in granulosa cells treated in vitro with luteinizing hormone, follicle-stimulating hormone, prolactin, or a combination. , 2006, Poultry science.

[17]  T. Yamazaki,et al.  Tributyltin disturbs bovine adrenal steroidogenesis by two modes of action , 2005, Steroids.

[18]  I. Yamamoto,et al.  cDNA Cloning and mRNA Expression of Estrogen Receptor α in Japanese Quail , 2003 .

[19]  H. Adlercreutz Phyto-oestrogens and cancer. , 2002, The Lancet. Oncology.

[20]  A. Johnson,et al.  Regulation of steroidogenic acute regulatory protein and luteinizing hormone receptor messenger ribonucleic acid in hen granulosa cells. , 2001, Endocrinology.

[21]  S. Inoue,et al.  Interaction of Phytoestrogens with Estrogen Receptors α and β , 2001 .

[22]  P. Shughrue,et al.  Comparative distribution of estrogen receptor‐α and ‐β mRNA in the rat central nervous system , 1997, The Journal of comparative neurology.

[23]  D. Long,et al.  Changes in plasma concentrations of luteinizing hormone, progesterone, and testosterone in turkey hens during the ovulatory cycle. , 1997, General and comparative endocrinology.

[24]  E. Adashi,et al.  Insulin-like growth factor-I-mediated amplification of follicle-stimulating hormone-supported progesterone accumulation by cultured rat granulosa cells: enhancement of steroidogenic enzyme activity and expression. , 1997, Biology of reproduction.

[25]  J. McLachlan,et al.  The estrogenic and antiestrogenic activities of phytochemicals with the human estrogen receptor expressed in yeast , 1997, Steroids.

[26]  K. Setchell,et al.  Biological effects of a diet of soy protein rich in isoflavones on the menstrual cycle of premenopausal women. , 1994, The American journal of clinical nutrition.

[27]  A. Johnson,et al.  Cytochrome P450 side-chain cleavage (P450scc) in the hen ovary. II. P450scc messenger RNA, immunoreactive protein, and enzyme activity in developing granulosa cells. , 1991, Biology of reproduction.

[28]  A. Johnson,et al.  Cytochrome P450 side-chain cleavage (P450scc) in the hen ovary. I. Regulation of P450scc messenger RNA levels and steroidogenesis in theca cells of developing follicles. , 1991, Biology of reproduction.

[29]  B. Marrone,et al.  Quantitative cytochemistry of 3 beta-hydroxysteroid dehydrogenase activity in avian granulosa cells during follicular maturation. , 1989, Biology of reproduction.

[30]  C. Hughes,et al.  Phytochemical mimicry of reproductive hormones and modulation of herbivore fertility by phytoestrogens. , 1988, Environmental health perspectives.

[31]  P Argos,et al.  The chicken oestrogen receptor sequence: homology with v‐erbA and the human oestrogen and glucocorticoid receptors. , 1986, The EMBO journal.

[32]  S. O'leary POISONING IN MAN FROM EATING POISONOUS PLANTS. PRESENT STATUS IN THE UNITED STATES: PRELIMINARY REPORT. , 1964, Archives of environmental health.