Source:http://linkedlifedata.com/resource/pubmed/id/20737414
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2011-2-25
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pubmed:abstractText |
Dextromethorphan is widely used in over-the-counter cough and cold medications. Its efficacy and safety for infants and young children remains to be clarified. The present study was designed to use zebrafish as a model to investigate the potential toxicity of dextromethorphan during embryonic and larval development. Three sets of zebrafish embryos/larvae were exposed to dextromethorphan at 24, 48 and 72?h post fertilization (hpf), respectively, during the embryonic/larval development. Compared with the 48 and 72?hpf exposure sets, the embryos/larvae in the 24?hpf exposure set showed much higher mortality rates which increased in a dose-dependent manner. Bradycardia and reduced blood flow were observed for the embryos/larvae treated with increasing concentrations of dextromethorphan. Morphological effects of dextromethorphan exposure, including yolk sac and cardiac edema, craniofacial malformation, lordosis, non-inflated swim bladder and missing gill, were also more frequent and severe among zebrafish embryos/larvae exposed to dextromethorphan at 24?hpf. Whether the more frequent and severe developmental toxicity of dextromethorphan observed among the embryos/larvae in the 24?hpf exposure set, as compared with the 48 and 72?hpf exposure sets, is due to the developmental expression of the phase I and phase II enzymes involved in the metabolism of dextromethorphan remains to be clarified. A reverse transcription-polymerase chain reaction analysis, nevertheless, revealed developmental stage-dependent expression of mRNAs encoding SULT3 ST1 and SULT3 ST3, two enzymes previously shown to be capable of sulfating dextrorphan, an active metabolite of dextromethorphan.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antitussive Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Dextromethorphan,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/SULT3 sulfotransferase, zebrafish,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfotransferases,
http://linkedlifedata.com/resource/pubmed/chemical/Teratogens,
http://linkedlifedata.com/resource/pubmed/chemical/Zebrafish Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1099-1263
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 John Wiley & Sons, Ltd.
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pubmed:issnType |
Electronic
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
157-63
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pubmed:meshHeading |
pubmed-meshheading:20737414-Animals,
pubmed-meshheading:20737414-Antitussive Agents,
pubmed-meshheading:20737414-Behavior, Animal,
pubmed-meshheading:20737414-Bradycardia,
pubmed-meshheading:20737414-Craniofacial Abnormalities,
pubmed-meshheading:20737414-Dextromethorphan,
pubmed-meshheading:20737414-Dose-Response Relationship, Drug,
pubmed-meshheading:20737414-Edema,
pubmed-meshheading:20737414-Edema, Cardiac,
pubmed-meshheading:20737414-Embryo, Nonmammalian,
pubmed-meshheading:20737414-Embryonic Development,
pubmed-meshheading:20737414-Feeding Behavior,
pubmed-meshheading:20737414-Gene Expression Regulation, Developmental,
pubmed-meshheading:20737414-Larva,
pubmed-meshheading:20737414-RNA, Messenger,
pubmed-meshheading:20737414-Regional Blood Flow,
pubmed-meshheading:20737414-Sulfotransferases,
pubmed-meshheading:20737414-Teratogens,
pubmed-meshheading:20737414-Yolk Sac,
pubmed-meshheading:20737414-Zebrafish,
pubmed-meshheading:20737414-Zebrafish Proteins
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pubmed:year |
2011
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pubmed:articleTitle |
Developmental toxicity of dextromethorphan in zebrafish embryos/larvae.
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pubmed:affiliation |
Department of Pharmacology, College of Pharmacy, The University of Toledo, Toledo, OH 43606 USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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