Volume 3, Issue 2 (7-2005)                   IJRM 2005, 3(2): 62-67 | Back to browse issues page

XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Babaei H, Derakhshanfar A, Nematollahi-Mahani S N, Nabipour F, Zeraatpisheh A. Morphologic changes in fresh and vitrified mouse ovaries after retinol palmitate administration. IJRM 2005; 3 (2) :62-67
URL: http://ijrm.ir/article-1-41-en.html
Abstract:   (2340 Views)
Background: Retinoids have been suggested to play a role in oogenesis and oocyte survival. Objective: In the present study the effects of retinol palmitate were investigated on differential follicular counts in response to superovulation as well as follicle quality after vitrification of ovaries. Materials and Methods: Ten, 4 week old female BALB/c mice were randomly assigned to either paraffin (n=5) or retinol palmitate (n=5) administration. Vitamin A administered animals received (i.p.) 250 IU retinol palmitate, dissolved in 0.1 ml of paraffin oil on days one and ten followed by superovulation with 10 IU PMSG. Paraffin administered mice were only treated with 0.1 ml of paraffin oil. The collected left ovaries from both paraffin and vitamin A administered groups were considered as non-vitrified and the collected right ovaries from both treated groups underwent vitrification. Ovaries in the vitrified group were frozen sequentially by placing into two vitrification solutions {VS1: 10% ethylene glycol (EG), 10% DMSO in holding medium (TCM-199 + 20% FBS: HM) and VS2: 20% EG, 20% DMSO in HM}. After warming, recovered ovaries as well as non-vitrified ovaries were serially sectioned and examined histopathologically. Results: The proportion of antral follicles in the non-vitrified ovaries from vitamin A administered mice was statistically higher than the non-vitrified ovaries from paraffin administered group (29.4% vs. 15.6%, respectively; p<0.001). No difference due to retinol palmitate injection was observed for the rate of small follicles between the two non-vitrified groups. The percentage of damaged follicles did not show any significant differences between the two vitrified groups (76% vs. 79%). Conclusions: Our results demonstrate that administration of retinol palmitate may improve the response to superovulation through the shift of follicular growth towards antral follicle development. However, no positive effect of retinol palmitate in the quality of follicles is probable when ovaries are vitrified.
Full-Text [PDF 698 kb]   (370 Downloads) |   |   Full-Text (HTML)  (281 Views)  
Type of Study: Original Article |

References
1. Blomhoff R. Overview of vitamin A metabolism and function. In: Blomhoff R. Vitamin A in health and disease, 1st Ed. New York: Marcel Dekker; 1994; 1-35. [DOI:10.1201/9781482277562] [PMCID]
2. Cudas LJ. Retinoids and vertebrate development. J Biol Chem 1994; 269: 15399-15402.
3. Ross SA, McCaffery PJ, Drager UC, De Luca LM. Retinoids in embryonal development. Physiol Rev 2000; 80: 1021-1054. [DOI:10.1152/physrev.2000.80.3.1021] [PMID]
4. Chew BP, Archer RG. Comparative role of vitamin A and β-carotene on reproductive and neonatal survival in rats. Therio 1983; 20: 459 (abstract). [DOI:10.1016/0093-691X(83)90205-4]
5. Besenfelder UL, Solti J, Seregi M, Brem G. Influence of β-carotene on fertility in rabbits when using embryo transfer programs. Therio 1993; 39: 1093-1109. [DOI:10.1016/0093-691X(93)90009-T]
6. Britt JH, Whaley SL, Hedgpeth VS. Improvement of embryo survival by injection of vitamin A in gilts fed normal or high energy diets before and after mating. J Anim Sci 1992; 641(suppl. 1): 271.
7. Coffey MT, Britt JH. Enhancement of sow reproductive performance by β-carotene or vitamin A. J Anim Sci 1993; 71: 1198-1202. [DOI:10.2527/1993.7151198x] [PMID]
8. Livera G, Rouiller-Fabre V, Valla J, Habert R. Effects of retinoids on meiosis in the fetal rat ovary in culture. Mol Cell Endocrinol 2000; 165: 225-231. [DOI:10.1016/S0303-7207(00)00271-9]
9. Hidalgo CO, Diez C, Duque P, Facal N, Gomez E. Pregnancies and improved early embryonic development with bovine oocytes matured in vitro with 9-cis-retinoic acid. Reproduction 2003; 125: 409-416. [DOI:10.1530/rep.0.1250409] [PMID]
10. Migishima F, Suzuki-Migishima R, Song SY, Kuramochi T, Azuma S, Nishijima M, Yokoyama M. Successful cryopreservation of mouse ovaries by vitrification. Biol Reprod 2003; 68: 881-887. [DOI:10.1095/biolreprod.102.007948] [PMID]
11. Deansely R. Immature rat ovaries grafted after freezing and thawing. Endocrinol 1957; 11: 197-200. [DOI:10.1677/joe.0.0110197] [PMID]
12. Parrot D.M. The fertility of mouse with orthopic ovarian grafts derived from frozen tissue. J Reprod Fertil 1960; 1: 230-241. [DOI:10.1530/jrf.0.0010230]
13. Candy CJ, Wood MJ, Whittingham DG. Effect of cryoprotectants on the survival of follicles in frozen mouse ovaries. J Reprod Fertil 1997; 110: 11-19. [DOI:10.1530/jrf.0.1100011] [PMID]
14. Critser JK, Arneson BW, Aaker DW, Ball GD. Cryopreservation of hamster oocytes: effects of vitrification or freezing on human sperm penetration of zona-free hamster oocytes. Fertil Steril 1986; 46: 277-284. [DOI:10.1016/S0015-0282(16)49526-9]
15. Nematallahi-Mahani SN, Saito H, Hiroi M. Vitrification of mouse ovarian tissue in ethylene glycol based solution, thawing, in vitro maturation of follicles and fertilization of oocytes. Fertil Steril 1999; 72 (suppl. 1): 200.
16. Sugimoto M, Maeda S, Manabe N, Miyamoto H. Development of infantile rat ovaries autotransplanted after cryopreservation by vitrification. Therio 2000; 53: 1093-1103. [DOI:10.1016/S0093-691X(00)00255-7]
17. Salehnia M, Abbasian Moghadam E, Rezazadeh Velojerdi M. Ultrastructural of follicles after vitrification of mouse ovarian tissue. Fertil Steril 2002; 78: 644-645. [DOI:10.1016/S0015-0282(02)03287-9]
18. Bos-Mikich A, Wood MJ, Candy CJ, Whittingham DG. Cytogenetical analysis and developmental potential of vitrified mouse oocytes. Biol Reprod 1995; 53: 780-785. [DOI:10.1095/biolreprod53.4.780] [PMID]
19. Elmarimi AA, Holdas JS, Ven E, Imrik P. Effect of vitamin A supplementation on mice embryo production and viability. Reprod Dom Anim 1990; 25: 247-248. [DOI:10.1111/j.1439-0531.1990.tb00468.x]
20. Vajta G, Holm F, Kuwayama M, Booth PJ, Jacobsen H, Greve T, Callesen H. Open pulled straw (OPS) vitrification: a new way to reduce cryoinjuries of bovine ova and embryos. Mol Reprod Dev 1998; 51: 53-58. https://doi.org/10.1002/(SICI)1098-2795(199809)51:1<53::AID-MRD6>3.0.CO;2-V [DOI:10.1002/(SICI)1098-2795(199809)51:13.0.CO;2-V]
21. Thomas JB, Brad B, Alen RW, James JC, Jerrold LH. Influence of sampling on the reproducibility of ovarian follicle counts in mouse toxicity studies. Reprod Toxicol 1997; 11: 689-696. [DOI:10.1016/S0890-6238(97)00034-8]
22. Baird DT, Webb BK, Campbell LM, Harkness LM, Gosden RG. Long-term ovarian function in sheep after ovariectomy and transplantation of autografts stored at -196C. Endocrinol 1999; 140: 462-471. [DOI:10.1210/endo.140.1.6453] [PMID]
23. Waterhouse T, Cox SL, Snow M, Jenkin G, Shaw J. Offspring produced from heterotopic ovarian allografts in male and female recipient mice. Reproduction 2004; 127: 689-694. [DOI:10.1530/rep.1.00081] [PMID]
24. Okamura H, Katabuchi H, Ohba T. What we have learned from isolated cells from human ovary?. Mol Cell Endocrinol 2003; 202: 37-45. [DOI:10.1016/S0303-7207(03)00060-1]
25. Schmidt KL, Yding Andersen C, Loft A, Byskov AG, Ernst E, Nyboe Andersen A. Follow-up of ovarian function post-chemotherapy following ovarian cryopreservation and transplantation. Hum Reprod 2005; 20: 3539-3546. [DOI:10.1093/humrep/dei250] [PMID]
26. Nugent D, Newton H, Gallivan L, Godsen R. Protective effect of vitamin E on ischaemia reperfusion injury in ovarian grafts. J Reprod Fertil 1998; 114: 341-346. [DOI:10.1530/jrf.0.1140341] [PMID]
27. Newton H, Illingworth P. In vitro growth of murine preantral follicles after isolation from cryopreserved ovarian tissue. Hum Reprod 2001; 16: 423-429. [DOI:10.1093/humrep/16.3.423] [PMID]
28. Schweigert FJ, Zucker H. Concentration of vitamin A injection before mating on oocyte development, follicular hormones and ovulation in gilts fed high-energy diets. J Anim Sci 1988; 78: 1598-1607. [DOI:10.2527/2000.7861598x] [PMID]
29. Shaw DW, Farin PW, Washburn SP, Britt JH. Effect of retinol palmitate on ovulation rate and embryo quality in superovulated cattle. Therio 1995; 44: 51-58. [DOI:10.1016/0093-691X(95)00147-Z]
30. Eberhardt DM, Will WA, Godsen GD. Retinol administration to superovulated ewes improves in vitro embryonic viability. Biol Reprod 1999; 60: 1483-1487. [DOI:10.1095/biolreprod60.6.1483] [PMID]
31. Whaley SL, Hedgpeth VS, Farin CE, Martus NS, Jayes FCL, Britt JH. Influence of vitamin A injection before mating on oocyte development, follicular hormones, and ovulation in gilts fed high energy diets. J Anim Sci 2000; 78: 1598-1607. [DOI:10.2527/2000.7861598x] [PMID]
32. Lima PF, Oliveira MAL, Goncalves PBD, Montagner MM, Reichenbach HD, et al. Effects of retinol on the in vitro development of Bos Indicus embryos to blastocysts in two different culture systems. Reprod Dom Anim 2004; 39: 356-360. [DOI:10.1111/j.1439-0531.2004.00528.x] [PMID]
33. Besenfelder UL, Solti J, Seregi M, Muller M, Brem G. Different roles for β-carotene and vitamin A in the reproduction of rabbits. Therio 1996; 45: 1583-1591. [DOI:10.1016/0093-691X(96)00127-6]
34. Brown BS, Whisnant CS, Reed BK. Effect of vitamin A injection on the response to superovulation in beef cattle. J Anim Sci 1997; 75(suppl. 1): 211.
35. Napoli JL. Retinoic acid biosynthesis and metabolism. FASEB J 1996; 10: 993-1001. [DOI:10.1096/fasebj.10.9.8801182] [PMID]
36. Noy N. Retinoid-binding proteins mediators of retinoid action. Biochem J 2000; 348: 481-495. [DOI:10.1042/bj3480481] [PMID] [PMCID]
37. Mangelsdrof D, Umesono K, Evans RM. The retinoid receptors. In: Sporn MB, Roberts AB, Goodman DS. Retinoids: Biology, chemistry and medicine, 2nd Ed. New York: Raven Press; 1994; 319-350.
38. Brown JA, Eberhardt DM, Shrick FN, Roberts MP, Godkin JD. Expression of retinol-binding protein and cellular retinol-binding protein in the bovine ovary. Mol Reprod Dev 2003; 64: 261-269. [DOI:10.1002/mrd.10225] [PMID]
39. Bagavandoss P, Midgley AR. Biphasic action of retinoids on gonadotropin receptor induction in rat granulosa cells in vitro. Life Sci 1988; 43: 1607-1614. [DOI:10.1016/0024-3205(88)90532-2]
40. Hafez ESE, Hafez B. Folliculogenesis, Egg maturation and Ovulation. In: Hafez ESE, Hafez B. Reproduction in Farm Animals, 7th Ed. Philadelphia: Lippincott Williams & Wilkins; 2000; 68-81. [DOI:10.1002/9781119265306.ch5]

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Designed & Developed by : Yektaweb