Effect of endocrine disruptors on the ratio of X and Y chromosome-bearing live spermatozoa
DC Field | Value | Language |
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dc.contributor.author | Song, W.-H. | - |
dc.contributor.author | Mohamed, E.A. | - |
dc.contributor.author | Pang, W.-K. | - |
dc.contributor.author | Kang, K.-H. | - |
dc.contributor.author | Ryu, D.-Y. | - |
dc.contributor.author | Rahman, M.S. | - |
dc.contributor.author | Pang, M.-G. | - |
dc.date.available | 2019-03-08T06:58:24Z | - |
dc.date.issued | 2018-12 | - |
dc.identifier.issn | 0890-6238 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/3458 | - |
dc.description.abstract | Although equal numbers of X and Y spermatozoa are produced during spermatogenesis, the sex chromosome ratio in ejaculated spermatozoa can be altered by exposure to endocrine-disrupting chemicals (EDCs), which can be reflected by altered sex ratios at birth. Here, we hypothesized EDCs affect sperm functions and viability of X and Y chromosome-bearing human spermatozoa. After exposure to genistein (Gen), bisphenol A (BPA), 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), dibromochloropropane (DBCP), and diazinon (Diaz), we evaluated motility, viability, capacitation, and differential viability of X and Y spermatozoa. All EDCs tested altered sperm viability, motility, and capacitation. Interestingly, the Y/X ratio of live spermatozoa was significantly lower in sperm treated with TCDD, DBCP, and Diaz than control spermatozoa. Our results suggest that some of EDCs have larger effects on the viability of Y spermatozoa than X spermatozoa, implicating that a reduction in Y sperm viability may result in a female-biased sex ratio of offspring at birth. © 2018 Elsevier Inc. | - |
dc.format.extent | 8 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Elsevier Inc. | - |
dc.title | Effect of endocrine disruptors on the ratio of X and Y chromosome-bearing live spermatozoa | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.reprotox.2018.09.002 | - |
dc.identifier.bibliographicCitation | Reproductive Toxicology, v.82, pp 10 - 17 | - |
dc.description.isOpenAccess | N | - |
dc.identifier.wosid | 000453648600002 | - |
dc.identifier.scopusid | 2-s2.0-85053796844 | - |
dc.citation.endPage | 17 | - |
dc.citation.startPage | 10 | - |
dc.citation.title | Reproductive Toxicology | - |
dc.citation.volume | 82 | - |
dc.type.docType | Article | - |
dc.publisher.location | 영국 | - |
dc.subject.keywordAuthor | Spermatozoa | - |
dc.subject.keywordAuthor | Sperm functions | - |
dc.subject.keywordAuthor | Sex chromosome | - |
dc.subject.keywordAuthor | Endocrine-disrupting chemical | - |
dc.subject.keywordAuthor | Sex ratio | - |
dc.subject.keywordPlus | PROTEIN-TYROSINE PHOSPHORYLATION | - |
dc.subject.keywordPlus | BISPHENOL-A AFFECTS | - |
dc.subject.keywordPlus | SEX-RATIO | - |
dc.subject.keywordPlus | HUMAN SPERM | - |
dc.subject.keywordPlus | GESTATIONAL EXPOSURE | - |
dc.subject.keywordPlus | OXIDATIVE STRESS | - |
dc.subject.keywordPlus | EPIDIDYMAL SPERM | - |
dc.subject.keywordPlus | IN-VIVO | - |
dc.subject.keywordPlus | ANEUPLOIDY | - |
dc.subject.keywordPlus | GENISTEIN | - |
dc.relation.journalResearchArea | Reproductive Biology | - |
dc.relation.journalResearchArea | Toxicology | - |
dc.relation.journalWebOfScienceCategory | Reproductive Biology | - |
dc.relation.journalWebOfScienceCategory | Toxicology | - |
dc.description.journalRegisteredClass | sci | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
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