6-Mercaptopurine Transport by Equilibrative Nucleoside Transporters in Conditionally Immortalized Rat Syncytiotrophoblast Cell Lines TR-TBTs
DC Field | Value | Language |
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dc.contributor.author | Lee, Na-Young | - |
dc.contributor.author | Sai, Yoshimichi | - |
dc.contributor.author | Nakashima, Emi | - |
dc.contributor.author | Ohtsuki, Sumio | - |
dc.contributor.author | Kang, Young-Sook | - |
dc.date.available | 2021-02-22T13:16:34Z | - |
dc.date.issued | 2011-09 | - |
dc.identifier.issn | 0022-3549 | - |
dc.identifier.issn | 1520-6017 | - |
dc.identifier.uri | https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/12508 | - |
dc.description.abstract | Recently, more women were provided with 6-mercaptopurine (6-MP) during pregnancy. Therefore, we attempted to clarify the transport mechanisms of 6-MP through blood-placenta barrier using rat conditionally immortalized syncytiotrophoblast cell lines (TR-TBTs). The uptake of 6-MP was time-and ATP dependent, but sodium independent in TR-TBTs. 6-MP was eliminated over 50% from the cells within 30 min. The uptake of 6-MP was saturable with Michaelis-Menten constant values of 198 : M and 250 : M in TR-TBT 18d-1 and TR-TBT 18d-2, respectively. 6-Thioguanine, azathioprine, and hypoxantine, structural analogues of 6-MP, strongly inhibited [C-14]6-MP uptake. Equilibrative nucleoside transporter (ENT) inhibitors, adenosine and uridine, significantly inhibited [C-14]6-MP uptake. However, several organic anions and cations had no effect on [C-14]6-MP uptake in TR-TBTs. These results suggest that sodium-independent transporters, ENTs, may be involved in 6-MP uptake at the placenta. In addition, multidrug resistance protein (MRP) inhibitors, methotrexate, probenecid, cefmeta-zole, and sulfinpyrazone, significantly increased the accumulation of [C-14]6-MP in the cells. It is indicated that 6-MP may be eliminated across the blood-placental barrier via MRPs. TR-TBTs expressed mRNA of ENT1, ENT2, MRP4, and MRP5. These findings are important for the therapy of acute lymphoblastic leukemia and autoimmune diseases of pregnant women, and should be useful data in elucidating teratogenicity of 6-MP during pregnancy. (C) 2011 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 100:3773-3782, 2011 | - |
dc.format.extent | 10 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | ELSEVIER SCIENCE INC | - |
dc.title | 6-Mercaptopurine Transport by Equilibrative Nucleoside Transporters in Conditionally Immortalized Rat Syncytiotrophoblast Cell Lines TR-TBTs | - |
dc.type | Article | - |
dc.publisher.location | 미국 | - |
dc.identifier.doi | 10.1002/jps.22631 | - |
dc.identifier.scopusid | 2-s2.0-79960136319 | - |
dc.identifier.wosid | 000294666600017 | - |
dc.identifier.bibliographicCitation | JOURNAL OF PHARMACEUTICAL SCIENCES, v.100, no.9, pp 3773 - 3782 | - |
dc.citation.title | JOURNAL OF PHARMACEUTICAL SCIENCES | - |
dc.citation.volume | 100 | - |
dc.citation.number | 9 | - |
dc.citation.startPage | 3773 | - |
dc.citation.endPage | 3782 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | sci | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Medicinal | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.subject.keywordPlus | BLOOD EFFLUX TRANSPORT | - |
dc.subject.keywordPlus | RESISTANCE PROTEIN | - |
dc.subject.keywordPlus | NUCLEOBASE ANALOGS | - |
dc.subject.keywordPlus | CHOLINE TRANSPORT | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | DRUGS | - |
dc.subject.keywordPlus | MRP4 | - |
dc.subject.keywordPlus | AZATHIOPRINE | - |
dc.subject.keywordPlus | METABOLITES | - |
dc.subject.keywordPlus | DISEASE | - |
dc.subject.keywordAuthor | placenta | - |
dc.subject.keywordAuthor | drug transport | - |
dc.subject.keywordAuthor | in vitro models | - |
dc.subject.keywordAuthor | pharmacokinetics | - |
dc.subject.keywordAuthor | nucleoside transporters | - |
dc.subject.keywordAuthor | organic anion transporters | - |
dc.subject.keywordAuthor | multidrug resistance-associated proteins | - |
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