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Successful vitrification of bovine blastocysts, derived by in vitro maturation and fertilization
Molecular reproduction and development, 1993-03, Vol.34 (3), p.266-271
Tachikawa, S.
Otoi, T.
Kondo, S.
Machida, T.
Kasai, M.
1993
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Tachikawa, S.
Otoi, T.
Kondo, S.
Machida, T.
Kasai, M.
Titel
Successful vitrification of bovine blastocysts, derived by in vitro maturation and fertilization
Ist Teil von
Molecular reproduction and development, 1993-03, Vol.34 (3), p.266-271
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
1993
Quelle
Wiley-Blackwell Journals
Beschreibungen/Notizen
Bovine blastocysts were produced through maturation, fertilization, and development in vitro. For vitrification, solutions designated EFS, GFS, and PFS were prepared; these were 40% ethylene glycol, 40% glycerol, and 40% propylene glycol, respectively, diluted in modified phosphate‐buffered saline (PBS) containing 30% Ficoll + 0.5 M sucrose. The embryos were exposed to the solutions in one step at room temperature, kept in the solutions for various times, vitrified in liquid nitrogen, and warmed rapidly. When the embryos were vitrified in EFS solution after 1 or 2 min exposure, the postwarming survival rate, assessed by the reexpansion of the blastocoel, was 74–77%. However, when the exposure time was extended to 3 min or longer, this rate dropped to 7–0%. This reduction was attributed to the toxicity of ethylene glycol. Of the embryos vitrified in GFS solution, 53% survived when they were cooled after 1 min exposure; as the duration of the exposure increased, the survival rate increased, reaching a peak (72%) at 4 min. The rate then decreased gradually with exposure time. In PFS solution, embryos surviving after vitrification were recovered only with 1 min exposure (33%), reflecting the high toxicity of propylene glycol. After vitrification in EFS or GFS solution, two embryos were nonsurgically transferred into each of 14 recipient animals. Of the 14 recipients, ten (71%) became pregnant; two resulted in early stillbirths, four recipients delivered twins (four alive and four stillborn), and two delivered single live calves, demonstrating the effectiveness of this simple vitrification method for the cryopreservation of in‐vitro‐produced bovine blastocysts. © 1993 Wiley‐Liss, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 1040-452X
eISSN: 1098-2795
DOI: 10.1002/mrd.1080340306
Titel-ID: cdi_proquest_miscellaneous_16546493
Format
–
Schlagworte
Animals
,
Biological and medical sciences
,
Blastocyst - cytology
,
Blastocyst - drug effects
,
blastocysts
,
Cattle
,
Cell Differentiation
,
Cryopreservation - methods
,
Cryoprotective Agents - toxicity
,
Early stages. Segmentation. Gastrulation. Neurulation
,
Embryo
,
Embryo Transfer
,
Embryology: invertebrates and vertebrates. Teratology
,
Ethylene glycol
,
Evaluation Studies as Topic
,
Female
,
fertilization
,
Fertilization in Vitro
,
Fundamental and applied biological sciences. Psychology
,
methodology
,
Pregnancy
,
Solutions
,
Vitrification
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