Literature DB >> 17926349

Live rats resulting from injection of oocytes with spermatozoa freeze-dried and stored for one year.

Shinichi Hochi1, Kaori Watanabe, Megumi Kato, Masumi Hirabayashi.   

Abstract

This study was designed to examine whether rat spermatozoa after freeze-drying and 1-year storage can participate in full-term development following intracytoplasmic sperm injection (ICSI). Cauda epididymal spermatozoa from Crlj:Wistar rats were frozen in liquid nitrogen (LN(2)), first dried for 14 hr at 0.37 hPa and then for 3 hr at 0.001 hPa. The dried spermatozoa were stored for 1 year in a desiccator at +25 degrees C, or in a refrigerator at +4 degrees C, or in LN(2) at -196 degrees C. Controls consisted of sperm that had only been frozen and stored in LN(2). After being stored, spermatozoa were sonicated to dissociate the sperm tail and were injected into oocytes from superovulated Slc:SD rats. The respective fertilization rates of oocytes injected with frozen sperm, or with freeze-dried sperm stored at +25, +4, and -196 degrees C were 79%, 75%, 70%, and 73%. However, the corresponding cleavage rates of injected oocytes were 63%, 1%, 38%, and 36%. After transfer of >80 zygotes of each group into recipients, the respective percentages of full-term normal offspring resulting from frozen sperm or from freeze-dried sperm stored at +25, +4, and -196 degrees C were 36%, 0%, 7%, and 14%. These results demonstrate that the storage temperature significantly influenced the likelihood of term development of rats produced by injection of oocytes with freeze-dried spermatozoa. Chromosomal analysis of the rat spermatozoa in the ICSI oocytes indicated that chromosomal aberration in freeze-dried spermatozoa stored at +25 degrees C (100%) occurred more frequently than in frozen control spermatozoa (41%) and freeze-dried spermatozoa stored at -196 degrees C (35%), and the frequency of chromosomal aberrations in freeze-dried spermatozoa stored at +4 degrees C (65%) was the intermediate. In conclusion, rat spermatozoa freeze-dried and stored at +4 degrees C for 1 year are capable of participating in full-term development after ICSI. (c) 2007 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2008        PMID: 17926349     DOI: 10.1002/mrd.20825

Source DB:  PubMed          Journal:  Mol Reprod Dev        ISSN: 1040-452X            Impact factor:   2.609


  14 in total

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

Authors:  Hiroyuki Watanabe; Tomoyoshi Asano; Yasuyuki Abe; Yutaka Fukui; Hiroshi Suzuki
Journal:  J Assist Reprod Genet       Date:  2009-10-24       Impact factor: 3.412

Review 2.  Dry Preservation of Spermatozoa: Considerations for Different Species.

Authors:  Jennifer Patrick; Pierre Comizzoli; Gloria Elliott
Journal:  Biopreserv Biobank       Date:  2017-02-27       Impact factor: 2.300

3.  High post-thaw survival of ram sperm after partial freeze-drying.

Authors:  Amir Arav; Antonella Idda; Stefano Mario Nieddu; Yehudit Natan; Sergio Ledda
Journal:  J Assist Reprod Genet       Date:  2018-03-14       Impact factor: 3.412

4.  The effects of cooling rates and type of freezing extenders on cryosurvival of rat sperm.

Authors:  Omer Varisli; Hollie Scott; Cansu Agca; Yuksel Agca
Journal:  Cryobiology       Date:  2013-05-30       Impact factor: 2.487

Review 5.  Chromosomal integrity and DNA damage in freeze-dried spermatozoa.

Authors:  Hirokazu Kusakabe
Journal:  Reprod Med Biol       Date:  2011-06-01

6.  Preservation of Mammalian Sperm by Freeze-Drying.

Authors:  Levent Keskintepe; Ali Eroglu
Journal:  Methods Mol Biol       Date:  2021

7.  Assessment of three generations of mice derived by ICSI using freeze-dried sperm.

Authors:  Ming-Wen Li; Brandon J Willis; Stephen M Griffey; Jimmy L Spearow; K C Kent Lloyd
Journal:  Zygote       Date:  2009-05-06       Impact factor: 1.442

8.  Live pups from evaporatively dried mouse sperm stored at ambient temperature for up to 2 years.

Authors:  Jie Liu; Gloria Y Lee; Joel A Lawitts; Mehmet Toner; John D Biggers
Journal:  PLoS One       Date:  2014-06-12       Impact factor: 3.240

9.  Develop to term rat oocytes injected with heat-dried sperm heads.

Authors:  Kyung-Bon Lee; Ki-Eun Park; In-Kiu Kwon; Swamy K Tripurani; Keun Jung Kim; Ji Hye Lee; Koji Niwa; Min Kyu Kim
Journal:  PLoS One       Date:  2013-11-04       Impact factor: 3.240

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

Authors:  Maite Olaciregui; Victoria Luño; Paula Domingo; Noelia González; Lydia Gil
Journal:  Sci Rep       Date:  2017-04-24       Impact factor: 4.379

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