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MELATONIN AND CHILD-BEARING. PART 1. PREIMPLANTATION PERIOD AND IMPLANTATION

https://doi.org/10.1234/XXXX-XXXX-2013-3-3-8

Abstract

Melatonin (M) — a hormone developed at land vertebrata and human in endocrine gland — pineal. It is established that one of the main functions M is synchronization of work of all bodies, regulation of seasonal and daily rhythms of their physiological activity. Function of synchronization and regulation of the rhythm is carried out according to a daily rhythm of an expression to the Mdepending on day and night length. The M is capable to influence growth, development and physiological activity of varios types of cell is similar to growth factors, influencing mechanisms of signaling pathways and cascades. It is confirmed that processes of conception, pregnancy and child-bearing directly depend on a rhythm an a profile of secretion of a pineal hormone of M in a organism. In this reveiew attempt to unite available in literary data of participation of M in various physiological processes durind preimplantation and post-implantation periods of life of an organism is undertaken, its positive and negative effects on puberty stages, gametogenese, fertilisation and implantation.

About the Authors

A. Yu. Molchanov

Russian Federation


M. G. Ivanovskaya
НИИ физико-химической биологии им. А.Н. Белозерского МГУ имени М.В. Ломоносова, 119991, г. Москва.
Russian Federation


References

1. Brzezinski A. Melatonin and human reproduction: why the effect is so elusive? // From molecules to therapy / Eds. S.R. Pandi-Perumal, D.P. Cardinali Melatonin. N.Y.: Nova Science Publishers, 2007. P. 219—225.

2. Silman R.E. Melatonin and the human gonadotrophin-releasing hormone pulse generator // J. Endocrinol. 1991. Vol. 128. P. 7—11.

3. Waldhauser F., Boepple P.A., Schemper M., Mansfield M.J., Crowley W.F.Jr. Serum melatonin in central precocious puberty is lower than in age-matched prepubertal // J. Clin. Endocrinol. Metab. 1991. Vol. 73. P. 793—796.

4. Cavallo A. Melatonin and human puberty. Current perspectives // J. Pineal. Res. 1993. Vol. 15. P. 115—121.

5. Cohen H.N., Hay I.D., Anneswley T.M. Serum immunoreactive melatonin in boys with delayed puberty // Clin. Endocrinol. 1982. Vol. 17. P. 291—297.

6. Diaz Lopez B., Diaz Rodriguez E., Urquijio C., Fernandez Alvarez C. Melatonin influences on the neuroendocrine—reproductive axis // Ann. N.Y. Acad. Sci. 2005. Vol. 1057. P. 337—364.

7. Reiter R.J. Pineal melatonin: cell biology of its synthesis and its physiological interactions // Endocrinol. Rev. 1991. Vol. 12. P. 151—180.

8. Roy D., Belsham D.D. Melatonin receptor activation regulates GnRH gene expression and secretion in GT1-7 GnRH neurons: signal transduction mechanisms // J. Biol. Chem. 2002. Vol. 277. P. 251—258.

9. Waldhauser F., Weiszenbacher G., Frish H., Zeithuber V., Waldhauser M., Wurtman R.J. Fall in the nocturnal serum melatonin during prepuberty and pubescence // Lancet. 1984. Vol. 1. P. 362—365.

10. Ayre E.A., Wang Z.P., Brown G.M., Pang S.F. Localization and characterization of [125I] iodomelatonin binding sites in duck gonads // J. Pineal. Res. 1994. Vol. 17. P. 39—47.

11. Ayre E.A., Pang S.F. 2-[125I] Iodoelatonin binding sites in the testis and ovaries: putatitive melatonin receptors in the gonads // Biol. Signals. 1994. Vol. 3. P. 71—84.

12. Takasaki A., Nakamura Y., Tamura H., Shimamura K., Morioka H. Melatonin as a new drug for improving oocyte quality // Reprod. Med. Biol. 2003. Vol. 2. P. 139—144.

13. Tamura H., Takasaki A., Miwa I., Taniguchi K., Maekawa R., Asada H. Oxidative stress impairs oocyte quality and melatonin protects oocytes from free radical damage and improves fertilization rate // J. Pineal. Res. 2008. Vol. 44. P. 280—287.

14. Хронобиология и хрономедицина: Руководство / Под ред. С.И. Рапопорта, В.А. Фролова, Л.Г. Хетагуровой. М.: ООО “Медицинское информационное агентство”, 2012. 480 с.

15. Woo M., Tai C.-J., Kang S., Nathwani P., Pang S., Leung P. Direct action of melatonin in human granulosa-luteal cells // J. Clinic. Endocrin. & Metab. 2008. Vol. 86. N 10. P. 4789—4797.

16. Chernyshov V.P., Tumanova L.E., Sudoma I.A., Bannikov V.I. Th1 and Th2 in Human IVF Pregnancy with Allogenic Fetus // Am. J. Reprod. Immunol. 2008. Vol. 59. N 4. P. 352—358.

17. Shiu S.Y.W., Li L., Wong J.T.Y., Pang S.F. Biology of G-protein coupled melatonin receptors in the epididymis and prostate of mammals // Chin. Med. J. 1997. Vol. 110. P. 648—655.

18. Luboshitzky R., Shen-Orr Z., Nave R., Lavi S., Lavie P. Melatonin administration alters semen quality in healthy men // J. Androl. 2002. Vol. 23. P. 572—578.

19. Luboshitzky R., Levi M., Shen-Orr Z., Blumenfeld Z., Herer P., Lavie P. Long-term melatonin administration does not alter pituitary-gonodal hormone secretion in normal en // Hum. Reprod. 2000. Vol. 15. P. 60—65.

20. Laudon M., Gilad E., Matzkin H., Braf Z., Zisapel N. Putatitive melatonin receptors in benign prostate tissue // J. Clin. Endocrinol. Metab. 1996. Vol. 81. P. 1336—1342.

21. Tamura H., Takasaki A., Miwa I., Taniguchi K., Maekawa R., Asada H., Taketani T., Matsuoka A., Yamagata Y., Shimamura K., Morioka H., Ishikawa H., Reiter R.J., Sugino N. Oxidative stress impairs oocyte quality and melatonin protects oocytes from free radical damage and improves fertilization rate // J. Pineal. Res. 2008. Vol. 44. N 3. P. 280—287.

22. Wunder D., Limoni C., Birkhдuser M. and the Swiss FIVNAT-Group. Lack of seasonal variations in fertilization, pregnancy andimplantation rates in women undergoing IVF // J. Hum. Rep. 2005. Vol. 20. N 11. P. 3122—3129.

23. Tamura H., Nakamura Y., Takiguchi S., Kashida S., Yamagata Y., Sugino N. Melatonin directly suppresses steroid production by preovulatory follicles in the cyclic hamster // J. Pineal. Res. 1998. Vol. 25. P. 135—141.

24. Nakamura Y., Tamura H., Takayama H., Kato H. Increased endogenous level of melatonin in preovulatory human follicles does not directly influence progesterone production // Fertil. Steril. 2003. Vol. 80. P. 1012—1016.

25. Brzezinski A., Lynch H.J., Seibel M.M., Deng M.H., Wurtman R.J. The circadian rhythm of plasma melatonin during the normal menstrual cycle and in amenorrheic women // J. Clin. Endocrinol. Metab. 1988. Vol. 66. P. 891—896.

26. Анисомов В.Н., Виноградов И.А. Старение женской репродуктивной системы и мелатонина. СПб.: Система, 2008. 44 с.

27. Dair E.L., Simoes R.S., Simoes M.J. Effects of melatonin on the endometrial morphology and embryo implantation in rats // Fertil Steril (in press).

28. Garcτιa-Perga~neda A., Pozo D., Guerrero J.M., Calvo J.R. Signal transduction for melatonin in human lymphocytes: involvement of a pertussis-toxin sensitive G protein // J. Immunol. 1997. Vol. 159. P. 3774—3781.

29. Barjavel M.J., Mamdouh Z., Raghbate N., Bakouche O. Differential expression of the melatonin receptor in human monocytes // J. Immunol. 1998. Vol. 160. P. 1191—1197.

30. Lopez-Gonzalez M.A., Calvo J.R., Segura J.J., Guerrero J.M. Characterization of melatonin binding sites in human peripheral blood neutrophils // Biotech. Ther. 1993. Vol. .P. 253—262.

31. Saito S. Cytokine network at the feto-maternal interface // J. Reprod. Immunol. 2001. Vol. 47. P. 87—103.

32. Petrovsky N., Harrison L. The chronobiology of human cytokine production // Int. Rev. Immunol. 1998. Vol. 16. P. 635—649.

33. Raghavendra V., Singh V., Kulkarni S.K., Agrewala J.N. Melatonin enhances Th2 cell mediated immune responses: lack of sensitivity to reversal by naltrexone or benzodiazepi- ne receptor antagonists // Mol. Cell. Biochem. 2001. Vol. 221. P. 57—62.

34. Stolwijk A., Reuvers M., Hamilton C., Jongbloet P., Hollanders J., Zeilhuis G. Seasonality in the results of in-vitro fertilization // Hum. Reprod. 1994. P. 2300—2305.


Review

For citations:


Molchanov A.Yu., Ivanovskaya M.G. MELATONIN AND CHILD-BEARING. PART 1. PREIMPLANTATION PERIOD AND IMPLANTATION. Vestnik Moskovskogo universiteta. Seriya 16. Biologiya. 2013;(3):3-8. (In Russ.) https://doi.org/10.1234/XXXX-XXXX-2013-3-3-8

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ISSN 0137-0952 (Print)