Literature DB >> 19556436

Cryopreserved ovarian tissues can maintain a long-term function after heterotopic autotransplantation in rat.

Xiaohui Deng1, Hua Zheng, Xuan Yu, Hongling Yu, Chengmei Zhang, Lan Chao, Ruichang Li, Wenjun Liu.   

Abstract

The functional longevity of cryopreserved ovarian grafts is one of the most challenging questions regarding ovarian transplantation at present. This study used a rat ovarian grafting model to investigate whether ovarian tissues from adult rats, which had been cryopreserved by vitrification and followed by heterotopic transplantation, could establish long-term hormone secretion and follicle development. Fresh and cryopreserved ovarian tissues were autologously transplanted under the kidney capsule. One-third of the animals in each group (sham-operated, fresh autografts, cryopreserved autografts, or castrated) were killed 5, 8, or 10 months after transplantation. Vaginal cytology, serum estradiol (E(2)), progesterone, and the morphology of the reproductive tract were used to assess ovarian function. Both fresh and cryopreserved ovarian grafts survived well in all the animal models with comparable proportion of follicles at each stage of folliculogenesis at all three time points. The serum E(2) and progesterone concentrations in the groups with fresh or cryopreserved grafts remained comparable with those in sham-operated controls at all investigated time points. However, a loss of grafts and primordial follicles following heterotopic transplantation was noted. In conclusion, the heterotopic autotransplantation of vitrified ovarian tissues from adult rat without vascular anastomosis can maintain long-term ovarian function and exert endocrine function in target organs, in spite of the reduction in follicle pool.

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Year:  2009        PMID: 19556436     DOI: 10.1530/REP-09-0151

Source DB:  PubMed          Journal:  Reproduction        ISSN: 1470-1626            Impact factor:   3.906


  3 in total

Review 1.  Fertility preservation among the cancer patients by ovarian tissue cryopreservation, transplantation, and follicular development.

Authors:  Ali Abedelahi; Mostafa Rezaei-Tavirani; Daryosh Mohammadnejad
Journal:  Iran J Cancer Prev       Date:  2013

2.  Vitrification of camel skin tissue for use as a resource for somatic cell nuclear transfer in Camelus dromedarius.

Authors:  Young-Bum Son; Yeon Ik Jeong; Yeon Woo Jeong; Xianfeng Yu; Lian Cai; Eun Ji Choi; Mohammad Shamim Hossein; Alex Tinson; Kuhad Kuldip Singh; Singh Rajesh; Al Shamsi Noura; Woo Suk Hwang
Journal:  In Vitro Cell Dev Biol Anim       Date:  2021-05-20       Impact factor: 2.416

3.  The Increased Expression of Connexin and VEGF in Mouse Ovarian Tissue Vitrification by Follicle Stimulating Hormone.

Authors:  Yanzhou Yang; Jie Chen; Hao Wu; Xiuying Pei; Qing Chang; Wenzhi Ma; Huiming Ma; Changchun Hei; Xiaomin Zheng; Yufang Cai; Chengjun Zhao; Jia Yu; Yanrong Wang
Journal:  Biomed Res Int       Date:  2015-10-11       Impact factor: 3.411

  3 in total

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