Butylparaben is toxic to porcine oocyte maturation and subsequent embryonic development following in vitro fertilization

Cited 36 time in scopus
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dc.contributor.authorPil Soo Jeong-
dc.contributor.authorSanghoon Lee-
dc.contributor.authorSoo-Hyun Park-
dc.contributor.authorMin Ju Kim-
dc.contributor.authorHyogu Kang-
dc.contributor.authorT Nanjidsuren-
dc.contributor.authorHee Chang Son-
dc.contributor.authorBong-Seok Song-
dc.contributor.authorD B Koo-
dc.contributor.authorBo Woong Sim-
dc.contributor.authorSun-Uk Kim-
dc.date.accessioned2020-09-24T03:19:15Z-
dc.date.available2020-09-24T03:19:15Z-
dc.date.issued2020-
dc.identifier.issn1422-0067-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/22665-
dc.description.abstractParabens are widely used in personal care products due to their antimicrobial effects. Although the toxicity of parabens has been reported, little information is available on the toxicity of butylparaben (BP) on oocyte maturation. Therefore, we investigated the effects of various concentrations of BP (0 μM, 100 μM, 200 μM, 300 μM, 400 μM, and 500 μM) on the in vitro maturation of porcine oocytes. BP supplementation at a concentration greater than 300 μM significantly reduced the proportion of complete cumulus cell expansion and metaphase II oocytes compared to the control. The 300 μM BP significantly decreased fertilization, cleavage, and blastocyst formation rates with lower total cell numbers and a higher rate of apoptosis in blastocysts compared to the control. The BP-treated oocytes showed significantly higher reactive oxygen species (ROS) levels, and lower glutathione (GSH) levels than the control. BP significantly increased the aberrant mitochondrial distribution and decreased mitochondrial function compared to the control. BP-treated oocytes exhibited significantly higher percentage of γ-H2AX, annexin V-positive oocytes and expression of LC3 than the control. In conclusion, we demonstrated that BP impaired oocyte maturation and subsequent embryonic development, by inducing ROS generation and reducing GSH levels. Furthermore, BP disrupted mitochondrial function and triggered DNA damage, early apoptosis, and autophagy in oocytes.-
dc.publisherMDPI-
dc.titleButylparaben is toxic to porcine oocyte maturation and subsequent embryonic development following in vitro fertilization-
dc.title.alternativeButylparaben is toxic to porcine oocyte maturation and subsequent embryonic development following in vitro fertilization-
dc.typeArticle-
dc.citation.titleInternational Journal of Molecular Sciences-
dc.citation.number0-
dc.citation.endPage3692-
dc.citation.startPage3692-
dc.citation.volume21-
dc.contributor.affiliatedAuthorPil Soo Jeong-
dc.contributor.affiliatedAuthorSanghoon Lee-
dc.contributor.affiliatedAuthorSoo-Hyun Park-
dc.contributor.affiliatedAuthorMin Ju Kim-
dc.contributor.affiliatedAuthorHyogu Kang-
dc.contributor.affiliatedAuthorHee Chang Son-
dc.contributor.affiliatedAuthorBong-Seok Song-
dc.contributor.affiliatedAuthorBo Woong Sim-
dc.contributor.affiliatedAuthorSun-Uk Kim-
dc.contributor.alternativeName정필수-
dc.contributor.alternativeName이상훈-
dc.contributor.alternativeName박수현-
dc.contributor.alternativeName김민주-
dc.contributor.alternativeName강효구-
dc.contributor.alternativeNameNanjidsuren-
dc.contributor.alternativeName손희창-
dc.contributor.alternativeName송봉석-
dc.contributor.alternativeName구덕본-
dc.contributor.alternativeName심보웅-
dc.contributor.alternativeName김선욱-
dc.identifier.bibliographicCitationInternational Journal of Molecular Sciences, vol. 21, pp. 3692-3692-
dc.identifier.doi10.3390/ijms21103692-
dc.subject.keywordApoptosis-
dc.subject.keywordButylparaben-
dc.subject.keywordIn vitro maturation-
dc.subject.keywordMitochondria-
dc.subject.keywordPorcine oocyte-
dc.subject.keywordROS-
dc.subject.localapoptosis-
dc.subject.localApoptosis-
dc.subject.localButylparaben-
dc.subject.localin vitro maturation-
dc.subject.localIn vitro maturation-
dc.subject.localMitochondria-
dc.subject.localmitochondria-
dc.subject.localPorcine oocyte-
dc.subject.localPorcine oocytes-
dc.subject.localReactive oxidative species-
dc.subject.localReactive oxygen species(ROS)-
dc.subject.localReactive oxygen species-
dc.subject.localReactive Oxygen Species (ROS)-
dc.subject.localReactive Oxygen Species-
dc.subject.localROS-
dc.subject.localReactive oxygen species (ROS)-
dc.subject.localreactive oxygen species-
dc.subject.localreactive oxygen species (ROS)-
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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