Testicular toxicity of di-(2-ethylhexyl)phthalate in young Sprague-Dawley rats
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Park, Jung Duck | - |
dc.contributor.author | Habeebu, S.S.M. | - |
dc.contributor.author | Klaassen, C.D. | - |
dc.date.accessioned | 2023-05-30T05:40:26Z | - |
dc.date.available | 2023-05-30T05:40:26Z | - |
dc.date.issued | 2002-02 | - |
dc.identifier.issn | 0300-483X | - |
dc.identifier.uri | https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/66613 | - |
dc.description.abstract | Di-(2-ethylhexyl)phthalate (DEHP), used widely in the manufacture of plastics, is a well-known reproductive toxicant. It causes apoptosis and loss of spermatogenic cells, resulting in testicular atrophy. Reports are scarce in the literature on the progression of apoptosis following repeated doses of phthalates. DEHP's mechanism of inducing testicular atrophy has been associated with depletion of zinc in the testis. ZnT-1 is a zinc transporter that is highly expressed in the testis. Thus, DEHP might exert its toxic effects on the testis by altering the expression of ZnT-1. In this regard, 25-day old Sprague-Dawley rats were given vehicle (5 ml corn-oil/kg, po) for 2, 7 and 14 days, or DEHP (2 g/5 ml corn-oil/kg, po) daily, for 1, ?, 3, 5, 7, 10 and 14 days. Zinc content in testes was determined by atomic absorption spectrophotometry, and ZnT-1 mRNA was quantified by the branched DNA signal amplification method. Body weight gain and testicular weight (absolute and relative) were significantly lower in DEHP-treated rats. DEHP produced morphological changes in the testis, including apoptosis, necrosis, and loss of spermatogenic cells, which resulted in testicular atrophy. Apoptotic index (AI: the percentage of apoptotic cells in seminiferous tubules), determined using the TUNEL technique, was markedly increased after l day (AI: control AI: 0.1-0.3%) followed by a peak at 3 days (AI: 11.5%) and a gradual decrease till 10 14 days (AI: 7-9%). Zinc content in testis was not changed l day after DEHP administration, but decreased significantly at later time points. No difference was found in ZnT-1 mRNA expression between control and DEHP-treated animals until day 14. Our results suggest that apoptosis, along with necrosis, plays an important role in the mechanism of testicular atrophy by DEHP. In addition, ZnT-1 mRNA expression was not altered by DEHP and therefore, it appears that ZnT-1 cannot account for the decrease in testicular Zn content. Pathological lesions and apoptosis occurred prior to the loss of zinc in testis, suggesting that zinc depletion might be a secondary effect of DEHP-induced testicular toxicity, rather than the cause. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved. | - |
dc.format.extent | 11 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | ELSEVIER SCI IRELAND LTD | - |
dc.title | Testicular toxicity of di-(2-ethylhexyl)phthalate in young Sprague-Dawley rats | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/S0300-483X(01)00567-4 | - |
dc.identifier.bibliographicCitation | TOXICOLOGY, v.171, no.2-3, pp 105 - 115 | - |
dc.description.isOpenAccess | N | - |
dc.identifier.wosid | 000174005100005 | - |
dc.identifier.scopusid | 2-s2.0-0037186347 | - |
dc.citation.endPage | 115 | - |
dc.citation.number | 2-3 | - |
dc.citation.startPage | 105 | - |
dc.citation.title | TOXICOLOGY | - |
dc.citation.volume | 171 | - |
dc.type.docType | Article | - |
dc.publisher.location | 아일랜드 | - |
dc.subject.keywordAuthor | di-(2-ethylhexyl) phthalate | - |
dc.subject.keywordAuthor | testicular atrophy | - |
dc.subject.keywordAuthor | apoptosis | - |
dc.subject.keywordAuthor | apoptotic index | - |
dc.subject.keywordAuthor | zinc transporter | - |
dc.subject.keywordAuthor | ZnT-1 | - |
dc.subject.keywordAuthor | spermatogenic cells | - |
dc.subject.keywordPlus | GERM-CELL APOPTOSIS | - |
dc.subject.keywordPlus | MONO-(2-ETHYLHEXYL) PHTHALATE | - |
dc.subject.keywordPlus | DI(2-ETHYLHEXYL) PHTHALATE | - |
dc.subject.keywordPlus | DI-2-ETHYLHEXYL PHTHALATE | - |
dc.subject.keywordPlus | CONFERS RESISTANCE | - |
dc.subject.keywordPlus | ZINC | - |
dc.subject.keywordPlus | ATROPHY | - |
dc.subject.keywordPlus | TESTIS | - |
dc.subject.keywordPlus | DEATH | - |
dc.subject.keywordPlus | TRANSPORTER | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalResearchArea | Toxicology | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.relation.journalWebOfScienceCategory | Toxicology | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
84, Heukseok-ro, Dongjak-gu, Seoul, Republic of Korea (06974)02-820-6194
COPYRIGHT 2019 Chung-Ang University All Rights Reserved.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.