Literature DB >> 19856094

Pronuclear formation of freeze-dried canine spermatozoa microinjected into mouse oocytes.

Hiroyuki Watanabe1, Tomoyoshi Asano, Yasuyuki Abe, Yutaka Fukui, Hiroshi Suzuki.   

Abstract

PURPOSE: The aim of the present study was to investigate the fertilizing capacity of fresh, frozen-thawed and freeze-dried canine spermatozoa.
METHODS: After canine spermatozoa were injected into mouse oocytes, the rates of oocyte activation, male pronuclear formation and chromosomal aberrations were investigated.
RESULTS: The rates of oocyte activation were comparable (90.6-100%), no matter the sperm type injected. The percentage of male pronuclear formation was higher (P < 0.001) in the freeze-dried spermatozoa (92.3%) than the fresh (61.5%) and frozen-thawed (69.2%) spermatozoa. However, the chromosomal damage in the oocytes injected with freeze-dried spermatozoa was higher (72.9%: P < 0.001) than with fresh (26.9%) and frozen-thawed (21.4%) spermatozoa.
CONCLUSIONS: These data indicate using mouse oocytes that freeze-dried canine spermatozoa may potentially fertilize canine oocytes although chromosomal damage is frequently generated.

Entities:  

Mesh:

Year:  2009        PMID: 19856094      PMCID: PMC2788692          DOI: 10.1007/s10815-009-9358-y

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  33 in total

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4.  Long-term preservation of mouse spermatozoa after freeze-drying and freezing without cryoprotection.

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8.  Activation, pronuclear formation, and development in vitro of pig oocytes following intracytoplasmic injection of freeze-dried spermatozoa.

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10.  Tolerance of the mouse sperm nuclei to freeze-drying depends on their disulfide status.

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  8 in total

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Journal:  Reprod Med Biol       Date:  2011-06-01

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7.  In vitro developmental ability of ovine oocytes following intracytoplasmic injection with freeze-dried spermatozoa.

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8.  Molecular and Histological Evaluation of Sheep Ovarian Tissue Subjected to Lyophilization.

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