Skip to main content
Log in

Effects of tea polyphenols on ovarian development in rats

  • Original Articles
  • Published:
Journal of Endocrinological Investigation Aims and scope Submit manuscript

Abstract

Tea is the most consumed beverage in the world. Tea polyphenols are the major constituents of tea leaves and have shown many potential healthy benefits. However, whether tea polyphenols influence ovarian follicle assembly and development and ovarian life span is unknown. To study the effect of tea polyphenols on ovarian follicle development and oocyte apoptosis, we investigated rat ovarian development of different ages [from postnatal day (PD)1 after birth to 10 months] after treatment with tea polyphenols. Our data showed that the percentage of unassembled follicles increased in the ovaries of 1 — and 2-day-old rats which were ip injected with tea polyphenols (50 mg/kg/d) or whose mothers were treated with tea polyphenols (100 mg/kg/d) by intragastric administration from the day 11 after the detection of vaginal plug till delivery. The percentage of primordial follicles increased, while that of developing follicles decreased in the ovaries of 4- and 8-day-old rats following peritoneal injection with tea polyphenols compared with controls. The ratio of terminal deoxynucleotidyltransferase-mediated dUTP nick-end labeling (TUNEL)-positive oocytes decreased in the ovaries of neonatal rats following tea polyphenol treatment. In the 3- and 10-month-old rat ovaries, the number of primordial follicles augmented, whereas that of atretic follicles decreased after the treatment for 4 weeks. These data suggest that tea polyphenols may inhibit the transition from primordial to developing follicles, extend the entire growth phase of a follicle, and reduce dominant follicle numbers per cycle to increase the reserve of germ cells, inhibit oocyte apoptosis and follicle atresia during ovarian development from birth to early aged, and retard climacterium in rats. Drinking even a small cup of tea per day may benefit to extent the productive life of ovary.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Kezele P, Skinner MK. Regulation of ovarian primordial follicle assembly and development by estrogen and progesterone: endocrine model of follicle assembly. Endocrinology 2003, 144: 3329–37.

    Article  PubMed  CAS  Google Scholar 

  2. McGee EA, Hsueh AJ. Initial and cyclic recruitment of ovarian follicles. Endocr Rev 2000, 21: 200–14.

    PubMed  CAS  Google Scholar 

  3. Forabosco A, Sforza C, De Pol A, et al. Morphometric study of the human neonatal ovary. Anat Rec 1991, 231: 201–8.

    Article  PubMed  CAS  Google Scholar 

  4. Perez GI, Maravei DV, Trbovich AM, Cidlowski JA, Tilly JL, Hughes FM Jr. Identification of potassium-dependent and -independent components of the apoptotic machinery in mouse ovarian germ cells and granulose cells. Biol Reprod 2000, 63: 1358–69.

    Article  PubMed  CAS  Google Scholar 

  5. Morita Y, Tilly JL. Oocyte apoptosis: like sand through an hourglass. Dev Biol 1999, 213: 1–17.

    Article  PubMed  CAS  Google Scholar 

  6. Vaskivuo TE, Tapanainen JS. Apoptosis in the human ovary. Reprod Biomed Online 2003, 6: 24–35.

    Article  PubMed  Google Scholar 

  7. Pepling ME, Spradling AC. Female mouse germ cells form synchronously dividing cysts. Development 1998, 125: 3323–8.

    PubMed  CAS  Google Scholar 

  8. McGee EA, Perlas E, LaPolt PS, Tsafriri A, Hsueh AJ. Follicle-stimulating hormone enhances the development of preantral follicles in juvenile rats. Biol Reprod 1997, 57: 990–8.

    Article  PubMed  CAS  Google Scholar 

  9. Rajah R, Glaser EM, Hirshfield AN. The changing architecture of the neonatal rat ovary during histogenesis. Dev Dyn 1992, 194: 177–92.

    Article  PubMed  CAS  Google Scholar 

  10. Wise PM. Alterations in proestrous LH, FSH, and prolactin surges in middle-aged rats. Proc Soc Exp Biol Med 1982, 169: 348–54.

    Article  PubMed  CAS  Google Scholar 

  11. Dudley SD. Responsiveness to estradiol in central nervous system of aging female rats. Neurosci Biobehav Rev 1982, 6: 39–45.

    Article  PubMed  CAS  Google Scholar 

  12. Lin YS, Tsai YJ, Tsay JS, Lin JK. Factors affecting the levels of tea polyphenol and caffeine in tea leaves. J Agric Food Chem 2003, 51: 1864–73.

    Article  PubMed  CAS  Google Scholar 

  13. Wang LF, Kim DM, Lee CY. Effects of heat processing and storage on flavanols and sensory qualities of green tea beverages. J Agric Food Chem 2000, 48: 4227–32.

    Article  PubMed  CAS  Google Scholar 

  14. Manning J, Roberts JC. Analysis of catechin content of commercial green tea products. J Herb Pharmacother 2003, 3: 19–32.

    Article  PubMed  CAS  Google Scholar 

  15. Katiyar SK, Elmets CA. Green tea polyphenolic antioxidants and skin photoprotection. Int J Oncol 2001, 18: 1307–13.

    PubMed  CAS  Google Scholar 

  16. Hernaez, JF, Xu, M, Dashwood, RH. Antimutagenic activity of tea towards 2-hydroxyamino-3-methylimidazo[4,5-f] quinoline: effect of tea concentration and brew time on electrophile scavenging. Mutat Res 1998, 402: 299–306.

    Article  PubMed  CAS  Google Scholar 

  17. Annabi B, Lachambre MP, Bousquet-Gagnon N, Page M, Gingras D, Beliveau R. Green tea polyphenol (-)-epigallocatechin 3-gallate inhibits MMP-2 secretion and MT1-MMP-driven migration in gliblastoma cells. Biochim Biophys 2002, 1542: 209–20.

    Article  CAS  Google Scholar 

  18. Nam S, Smith DM, Dou QP. Ester bone-containing tea polyphenol potently inhibit proteasome activity in vitro and in vivo. J Biol Chem 2001, 276: 13322–30.

    Article  PubMed  CAS  Google Scholar 

  19. Otsuka T, Ogo T, Eto T, Asano Y, Suganuma M, Niho Y. Growth inhibition of leukemic cells by (−)-epigallocatechin gallate, the main constituent of green tea. Life Sci 1998, 63: 1397–403.

    Article  PubMed  CAS  Google Scholar 

  20. Liang YC, Lin-Shiau SY, Chen CF, Lin JK. Inhibition of cyclin-dependent kinases 2 and 4 activities as well as induction of Cdk inhibitors p21 and p27 during growth arrest of human breast carcinoma cells by (−)-epigallocatechin-3-gallate. J Cell Biochem 1999, 75: 1–12.

    Article  PubMed  CAS  Google Scholar 

  21. Ahmad N, Cheng P, Mukhtar H. Cell cycle dysregulation by green tea polyphenol epigallocatechin-3-gallate. Biochem Biophys Res Commun 2000, 275: 328–34.

    Article  PubMed  CAS  Google Scholar 

  22. Basini G, Bianco F, Grasselli F. EGCG, a major component of green tea, inhibits VEGF production by swine granulosa cells. Biofactors 2005, 23: 25–33.

    Article  PubMed  CAS  Google Scholar 

  23. Zhou XR, Gong ZJ, Yuan GJ, Sun XM. Study of protective role and its mechanism of tea polyphenol and EGCG in rats with alcohol-induced liver disease. China J Modem Medicine 2006, 16: 840–3.

    CAS  Google Scholar 

  24. Zhou XR, Gong ZJ, Yuan GJ, et al. Effects of tea polyphenol on alcoholic liver injury in rats. World Chin J Digestology 2006, 14: 50–6.

    CAS  Google Scholar 

  25. Parkening TA. Reproductive senescence in the Chinese hamster (Cricetulus griseus). J Gerontol 1982, 37: 283–7.

    Article  PubMed  CAS  Google Scholar 

  26. Kao YH, Hiipakka RA, Liao S. Modulation of endocrine systems and food intake by green tea epigallocatechin gallate. Endocrinology 2000, 141: 980–7.

    PubMed  CAS  Google Scholar 

  27. Aneja R, Hake PW, Burroughs TJ, Denenberg AG, Wong HR, Zingarelli B. Epigallocatechin, a green tea polyphenol, attenuates myocardial ischemia reperfusion injury in rats. Mole Med 2004, 10: 55–62.

    Article  CAS  Google Scholar 

  28. Hegarty VM, May HM, Khaw KT. Tea drinking and bone mineral density in older women. Am J Clin Nutr, 2000, 71: 1003–7.

    PubMed  CAS  Google Scholar 

  29. Fujiki H. Green tea: health benefits as cancer preventive for humans. Chem Rec 2005, 5: 119–32.

    Article  PubMed  CAS  Google Scholar 

  30. Kezele P, Skinner MK. Regulation of ovarian primordial follicle assembly and development by estrogen and progesterone: endocrine model of follicle assembly. Endocrinology 2003, 144: 3329–37.

    Article  PubMed  CAS  Google Scholar 

  31. Oktay K, Newton H, Mullan J, Gosden RG. Development of human primordial follicles to antral stages in SCID/hpg mice stimulated with follicle-stimulating hormone. Hum Reprod 1998, 13: 1133–8.

    Article  PubMed  CAS  Google Scholar 

  32. Yu YS, Sui HS, Han ZB, Li W, Luo MJ, Tan JH. Apoptosis in granulosa cells during follicular atresia: relationship with steroids and insulin-like growth factors. Cell Res 2004, 14: 341–6.

    Article  PubMed  CAS  Google Scholar 

  33. Chamoun D, Demoura MD, Levitas E, et al. Transcriptional and posttranscriptional regulation of intraovarian insulin-like growth factor-binding proteins by interleukin-1beta (IL-1beta): evidence for IL-1beta as an antiatretic principal. Endocrinology 1999, 140: 3488–95.

    PubMed  CAS  Google Scholar 

  34. Burke CR, Cardenas H, Mussard ML, Day ML. Histological and steroidogenic changes in dominant ovarian follicles during oestradial-induced atresia in heifers. Reproduction 2005, 129: 611–20.

    Article  PubMed  CAS  Google Scholar 

  35. Robles R, Morita Y, Mann KK, et al. The aryl hydrocarbon receptor, a basic helix-loop-helix transcription factor of the PAS gene family, is required for normal ovarian germ cell dynamics in the mouse. Endocrinology 2000, 141: 450–3.

    Article  PubMed  CAS  Google Scholar 

  36. Marcondes FK, Bianchi FJ, Tanno AP. Determintion of the estrous cycle phases of rats: some helpful considerations. Braz J Biol 2002, 62: 609–14.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to L. L. Luo MD.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Luo, L.L., Huang, J., Fu, Y.C. et al. Effects of tea polyphenols on ovarian development in rats. J Endocrinol Invest 31, 1110–1118 (2008). https://doi.org/10.1007/BF03345661

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF03345661

Keywords

Navigation