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Effect of Thiol Compounds on in Vitro Development and Intracellular Glutathione Content of Bovine Embryos
Author(s) -
Masashi Takahashi,
Taku Nagai,
Seizo HAMANO,
Masashige Kuwayama,
Naomichi Okamura,
Akira Okano
Publication year - 1993
Publication title -
biology of reproduction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.366
H-Index - 180
eISSN - 1529-7268
pISSN - 0006-3363
DOI - 10.1095/biolreprod49.2.228
Subject(s) - glutathione , cysteamine , blastocyst , buthionine sulfoximine , intracellular , embryo , biology , in vitro , thiol , human fertilization , andrology , embryogenesis , biochemistry , cytoplasm , microbiology and biotechnology , anatomy , enzyme , medicine
The purpose of this investigation was to determine the effect of beta-mercaptoethanol (beta-ME) and cysteamine, low-molecular-weight thiol compounds, on the development and intracellular glutathione content of bovine embryos obtained by in vitro fertilization of in vitro-matured oocytes. Embryos developed to the 6-8-cell stage after in vitro fertilization were cultured without feeder cells in TCM-199 containing 10% fetal calf serum with or without beta-ME or cysteamine. The percentage of embryos that developed to the blastocyst and hatched blastocyst stages were significantly higher in medium containing beta-ME or cysteamine. Also, total intracellular glutathione levels were higher for embryos cultured in the medium with beta-ME or cysteamine than for those cultured in medium without thiol compounds. Moreover, when buthionine sulfoximine, a specific inhibitor of glutathione synthesis, was added to medium containing thiol compounds, there was a reduction both in the development of embryos to the blastocyst stage and in intracellular glutathione content. These results indicate that the inclusion of low-molecular-weight thiol compounds aids the in vitro development of bovine embryos without feeder cells and that the effect of thiol compounds is mediated through the increase of intracellular glutathione levels.

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