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Czasopismo

2011 | 70 | 2 |

Tytuł artykułu

Assessment of morphological and functional changes in neonate vitrified testis grafts after host treatment with melatonin

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
This study was conducted to assess the effect of melatonin on the structure of testis and spermatogenesis dynamics in neonate vitrified testis grafts. Neonate vitrified testes, candidates for transplantation heterotopically to experiment or control groups, were warmed in thawing media which had or did not have a supplement of 100 µM melatonin, respectively. Following transplantation, melatonin (20 mg/kg/day) or saline solution was intraperitoneally injected into the treated and the non-treated groups, respectively. The initiating spermatogenesis, spermatogonia survival, and structure of tissue in the testis graft were examined. Cell apoptosis (TUNEL assay) and proliferation (Brdu assay) in germ cells were determined. Histological studies revealed the dynamic of the spermatogenesis process in the vitrified testis graft. However, dilation of the lumen accompanied by a disorganised epithelium in the non-treated group was higher than in the treated group. Furthermore, the proportion of apoptotic germ cells together with a reduced proportion of proliferated germ cells was higher in the non-treated group than in the treated group. Overall, the number of seminiferous tubules in the testes grafts of both groups remained steady. However, the non-treated testes grafts contained more damaged seminiferous tubules than the treated ones. The thickness of the seminiferous tubules was greater in the melatonin treated group than in the non-treated group. In fact, the thickness of germinal epithelium was significantly higher in the treated group than in the non-treated group. The study may show a positive effect from melatonin resulting in more grafts restoring puberty. Furthermore, the associated increase in the healthy number of seminiferous tubules suggests that melatonin may have a preventative ischaemia/antioxidant role and in fact may be useful to initiate the spermatogenesis process. (Folia Morphol 2011; 70, 2: 95–102)

Słowa kluczowe

Wydawca

-

Czasopismo

Rocznik

Tom

70

Numer

2

Opis fizyczny

p.95-102,fig.,ref.

Twórcy

autor
  • Fertility and Sterility Centre, Department of Perinatology, Imam Khomeini Hospital, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
  • Department of Anatomy, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
autor
  • Fertility and Sterility Centre, Department of Perinatology, Imam Khomeini Hospital, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
autor
  • Department of Animal Sciences, School of Agriculture, University of Mohghegh Ardabili, Iran
autor
  • Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  • Department of Anatomy,Faculty of Medicine, Tehran University of Medical Sciences, Poursina Street, 16 Azar Street, Enquelab Square,Tehran, Iran

Bibliografia

  • 1. Ahmad R, Haldar C (2010) Effect of intra-testicular melatonin injection on testicular functions, local and general immunity of a tropical rodent Funambulus pennanti. Endocrine, 37: 479–488.
  • 2. Baydas G, Reiter RJ, Yasar A, Tuzcu M, Akdemir I, Nedzvetskii VS (2003) Melatonin reduces glial reactivity in the hippocampus, cortex, and cerebellum of streptozotocin-induced diabetic rats. Free Radic Biol Med, 35: 797–804.
  • 3. Brown NS, Bicknell R (2001) Hypoxia and oxidative stress in breast cancer. Oxidative stress: its effects on the growth, metastatic potential and response to therapy of breast cancer. Breast Cancer Res, 3: 323–327.
  • 4. Cagnacci A, Volpe A (1996) Influence of melatonin and photoperiod on animal and human reproduction. J Endocrinol Invest, 19: 382–411.
  • 5. Cameron DF, Murray FT, Drylie DD (1985) Interstitial compartment pathology and spermatogenic disruption in testes from impotent diabetic men. Anat Rec, 213: 53–62.
  • 6. Frederickx V, Michiels A, Goossens E, De Block G, Van Steirteghem AC, Tournaye H (2004) Recovery, survival and functional evaluation by transplantation of frozen-thawed mouse germ cells. Hum Reprod, 19: 948–953.
  • 7. Ghosh S, Karin M (2002) Missing pieces in the NF-kappaB puzzle. Cell, 109: 81–96.
  • 8. Gosden RG, Baird DT, Wade JC, Webb R (1994) Restoration of fertility to oophorectomized sheep by ovarian autografts stored at –196 degrees C. Hum Reprod, 9: 597–603.
  • 9. Hemadi M, Abolhassani F, Akbari M, Sobhani A, Pasbakhsh P, Ahrlund-Richter L, Modaresi MH, Salehnia M (2009) Melatonin promotes the cumulus-oocyte complexes quality of vitrified-thawed murine ovaries; with increased mean number of follicles survival and ovary size following heterotopic transplantation. Eur J Pharmacol, 618: 84–90.
  • 10. Hemadi M, Saki G (2010) Endocrine function and duration time of estrous cyclicity of the ovariectomized recipiented neonate vitrified ovarian grafts mice after treatment with melatonin. Int J Pharmacol, 6: 379–385.
  • 11. Hemadi M, Saki G, Shokri S, Ghasemi FM (2011) Follicular dynamics in neonate vitrified ovarian grafts after host treatment with melatonin. Folia Morphol, 70: 18–23.
  • 12. Israely T, Dafni H, Granot D, Nevo N, Tsafriri A, Neeman M (2003) Vascular remodeling and angiogenesis in ectopic ovarian transplants: a crucial role of pericytes and vascular smooth muscle cells in maintenance of ovarian grafts. Biol Reprod, 68: 2055–2064.
  • 13. Li Z, Nickkholgh A, Yi X, Bruns H, Gross ML, Hoffmann K, Mohr E, Zorn M, Büchler MW, Schemmer P (2009) Melatonin protects kidney grafts from ischemia/reperfusion injury through inhibition of NF-kB and apoptosis after experimental kidney transplantation. J Pineal Res, 46: 365–372.
  • 14. Miragem A, Neto BS, Reche M, Kliemann LM, Capp E, von Eye Corleta H (2009) Subcutaneous autologous testicle transplantation in Wistar rats. Int Urol Nephrol, 41: 313–318.
  • 15. Palmeira CM, Santos DL, Seiça R, Moreno AJ, Santos MS (2001) Enhanced mitochondrial testicular antioxidant capacity in Goto-Kakizaki diabetic rats: role of coenzyme Q. Am J Physiol Cell Physiol, 281: 1023–1028.
  • 16. Reiter RJ (1993) Interactions of the pineal hormone melatonin with oxygen-centered free radicals: a brief review. Braz J Med Biol Res, 26: 1141–1155.
  • 17. Reiter RJ, Tan DX, Osuna C, Gitto E (2000) Actions of melatonin in the reduction of oxidative stress. J Biomed Sci, 7: 444–458.
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  • 20. Seethalakshmi L, Menon M, Diamond D (1987) The effect of streptozotocin-induced diabetes on the neuroendocrine — male reproductive tract axis of the adult rat. J Urol, 138: 190–194.
  • 21. Shrilatha B, Muralidhara (2007) Early oxidative stress in testis and epididymal sperm in streptozotocin-induced diabetic mice: its progression and genotoxic consequences. Reprod Toxicol, 23: 578–587.
  • 22. Stern JA, Lui RC, LaRegina MC, Herbold DR, Tolman KC, Johnson FE (1990) Long-term outcome following testicular ischemia in the rat. J Androl, 11: 390.
  • 23. Turner TT, Lysiak JJ (2008) Oxidative stress: a common factor in testicular dysfunction. J Androl, 29: 488–498.
  • 24. Wu B, Iwakiri R, Tsunada S, Utsumi H, Kojima M, Fujise T, Ootani A, Fujimoto K (2002) iNOS enhances rat intestinal apoptosis after ischemia-reperfusion. Free Radic Biol Med, 33: 649–658.
  • 25. Wyns C, Curaba M, Vanabelle B, Van Langendonckt A, Donnez J (2010) Options for fertility preservation in prepubertal boys. Hum Reprod Update, 16: 312–328.
  • 26. Yin H, Wang X, Kim SS, Chen H, Tan SL, Gosden RG (2003) Transplantation of intact rat gonads using vascular anastomosis: effects of cryopreservation, ischaemia and genotype. Hum Reprod, 18: 1165–1172.
  • 27. Yu J, Cai ZM, Wan HJ, Zhang FT, Ye J, Fang JZ, Gui YT, Ye JX (2006) Development of neonatal mouse and fetal human testicular tissue as ectopic grafts in immunodeficient mice. Asian J Androl, 8: 393–403.

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Typ dokumentu

Bibliografia

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