Exogenous gamma-tocotrienol promotes preimplantation development and improves the quality of porcine embryos

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dc.contributor.authorE Lee-
dc.contributor.authorS H Min-
dc.contributor.authorBong-Seok Song-
dc.contributor.authorJ Y Yeon-
dc.contributor.authorJ W Kim-
dc.contributor.authorJ H Bae-
dc.contributor.authorS Y Park-
dc.contributor.authorY H Lee-
dc.contributor.authorSun-Uk Kim-
dc.contributor.authorD S Lee-
dc.contributor.authorKyu Tae Chang-
dc.contributor.authorD B Koo-
dc.date.accessioned2017-04-19T10:08:48Z-
dc.date.available2017-04-19T10:08:48Z-
dc.date.issued2015-
dc.identifier.issn1031-3613-
dc.identifier.uri10.1071/RD13167ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/12733-
dc.description.abstractγ-tocotrienol (GTT), an isomer of vitamin E, has been the subject of increasing interest due to its strong anti-oxidant effects. Therefore, in this study, the effects of GTT on blastocyst development, expression levels of reactive oxygen species (ROS) and apoptotic index were investigated in preimplantation porcine embryos. After in vitro maturation and fertilisation, porcine embryos were cultured for 6 days in porcine zygote medium 3 supplemented with or without GTT (200μM) under oxidative stress conditions (200μM hydrogen peroxide (H2O2)). Blastocyst development was significantly improved in the GTT-treated group when compared with the H2O2-treated group (P<0.05). Subsequent evaluation of the intracellular levels of ROS and numbers of apoptotic nuclei in GTT-treated blastocysts revealed that ROS levels of GTT-treated porcine blastocysts were decreased (P<0.05) and the numbers of apoptotic nuclei were reduced by GTT treatment in porcine embryos. Moreover, the total cell numbers of blastocysts were significantly increased in the GTT-treated group relative to the untreated group under H2O2-induced oxidative stress (P<0.05). The expression levels of apoptosis-related genes (BCL-XL, BAX) in GTT-treated blastocysts were then investigated using real-time reverse transcription polymerase chain reaction. Expression of the anti-apoptotic BCL-XL gene was shown to be increased in the GTT-treated blastocyst group, whereas expression of the pro-apoptotic BAX gene was decreased. Taken together, these results suggest that GTT (200μM) under H2O2-induced oxidative stress, thereby improving the developmental competence of porcine embryos via modulation of intracellular levels of ROS and the apoptotic index during the preimplantation stage.-
dc.publisherCSIRO Publishing-
dc.titleExogenous gamma-tocotrienol promotes preimplantation development and improves the quality of porcine embryos-
dc.title.alternativeExogenous gamma-tocotrienol promotes preimplantation development and improves the quality of porcine embryos-
dc.typeArticle-
dc.citation.titleReproduction Fertility and Development-
dc.citation.number3-
dc.citation.endPage490-
dc.citation.startPage481-
dc.citation.volume27-
dc.contributor.affiliatedAuthorBong-Seok Song-
dc.contributor.affiliatedAuthorSun-Uk Kim-
dc.contributor.affiliatedAuthorKyu Tae Chang-
dc.contributor.alternativeName이은옥-
dc.contributor.alternativeName민성훈-
dc.contributor.alternativeName송봉석-
dc.contributor.alternativeName연지영-
dc.contributor.alternativeName김진우-
dc.contributor.alternativeName배정호-
dc.contributor.alternativeName박수영-
dc.contributor.alternativeName이용희-
dc.contributor.alternativeName김선욱-
dc.contributor.alternativeName이동석-
dc.contributor.alternativeName장규태-
dc.contributor.alternativeName구덕본-
dc.identifier.bibliographicCitationReproduction Fertility and Development, vol. 27, no. 3, pp. 481-490-
dc.identifier.doi10.1071/RD13167-
dc.subject.keywordantioxidant-
dc.subject.keywordapoptosis-
dc.subject.localAntioxidants-
dc.subject.localantioxidant-
dc.subject.localAnti-oxidant-
dc.subject.localantioxidants-
dc.subject.localANTIOXIDANT-
dc.subject.localanti-oxidants-
dc.subject.localAntioxidant-
dc.subject.localapoptosis-
dc.subject.localApoptosis-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Futuristic Animal Resource & Research Center > 1. Journal Articles
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