Literature DB >> 10079127

Kinetic and temporal factors influence chilling injury to germinal vesicle and mature bovine oocytes.

Y Zeron1, M Pearl, A Borochov, A Arav.   

Abstract

In this study we examined the effects of low, above freezing temperatures on the viability and functionality of bovine oocytes. Germinal vesicle (GV) stage and in vitro matured oocytes (MII) were exposed to various combinations of time (15 and 60 min) and temperature (4, 16, 23, and 39 degrees C). After being treated, the ability of oocytes to undergo maturation and fertilization in vitro was examined, as well as their viability assayed by two fluorescent probes, fluorescein diacetate (FDA) and 5-carboxyfluorescein diacetate (cFDA). Cooling GV oocytes to 16 degrees C for 15 min reduced the fertilization rate by more than 40%, compared with those left at 39 degrees C. Surprisingly, cooling oocytes to 4 degrees C reduced the fertilization rate by only 10% compared with control. Exposing GV oocytes to temperatures below 23 degrees C reduced their viability. Similar to the reduction in fertilization, the viability of GV oocytes after exposure to 16 degrees C was reduced by more than 50%, whereas exposure to 4 degrees C reduced it by only 9%. Viability measurements using FDA and cFDA gave comparable results and showed a similar trend. The viability of MII oocytes and of GV oocytes pretreated with butylated hydroxytoluene, following exposure to low temperatures, was higher compared with that of GV controls. We interpret these results as indicating chilling effects on membrane integrity. Improving the chilling resistance of bovine oocytes may facilitate their short- and long-term preservation. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10079127     DOI: 10.1006/cryo.1998.2139

Source DB:  PubMed          Journal:  Cryobiology        ISSN: 0011-2240            Impact factor:   2.487


  6 in total

1.  Apoptosis in cooled porcine oocytes: role of calcium (Ca2+) and Ca2+-dependent enzymes.

Authors:  B Barboni; M Mattioli; L Gioia; M Turriani; G Capacchietti; P Lucidi
Journal:  Vet Res Commun       Date:  2003-09       Impact factor: 2.459

Review 2.  Oocyte cryopreservation: searching for novel improvement strategies.

Authors:  Natalie A Clark; Jason E Swain
Journal:  J Assist Reprod Genet       Date:  2013-06-19       Impact factor: 3.412

3.  Human Sperm Cryopreservation: Update on Techniques, Effect on DNA Integrity, and Implications for ART.

Authors:  Marlea Di Santo; Nicoletta Tarozzi; Marco Nadalini; Andrea Borini
Journal:  Adv Urol       Date:  2011-12-13

4.  Cholesterol added prior to vitrification on the cryotolerance of immature and in vitro matured bovine oocytes.

Authors:  Núria Arcarons; Roser Morató; Meritxell Vendrell; Marc Yeste; Manel López-Bejar; Kosala Rajapaksha; Muhammad Anzar; Teresa Mogas
Journal:  PLoS One       Date:  2017-09-14       Impact factor: 3.240

5.  Successful vitrification of pronuclear-stage pig embryos with a novel cryoprotective agent, carboxylated ε-poly-L-lysine.

Authors:  Maki Kamoshita; Tsubasa Kato; Katsuyoshi Fujiwara; Takafumi Namiki; Kazuaki Matsumura; Suong-Hyu Hyon; Junya Ito; Naomi Kashiwazaki
Journal:  PLoS One       Date:  2017-04-27       Impact factor: 3.240

Review 6.  Cryopreservation and its clinical applications.

Authors:  Tae Hoon Jang; Sung Choel Park; Ji Hyun Yang; Jung Yoon Kim; Jae Hong Seok; Ui Seo Park; Chang Won Choi; Sung Ryul Lee; Jin Han
Journal:  Integr Med Res       Date:  2017-01-10
  6 in total

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