Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2006-9-25
pubmed:abstractText
We previously determined that the dithiocarbamate pesticide sodium metam (NaM) and its active ingredient methylisothiocyanate (MITC) were developmentally toxic causing notochord distortions in the zebrafish. In this study, developing zebrafish were exposed to isothiocyanates (ITCs), dithiocarbamates (DTCs) and several degradation products to determine the teratogenic relationship of these chemical classes at the molecular level. All dithiocarbamates tested elicited notochord distortions with notochord NOELs from <4 to 40 ppb, while none of the ITCs caused notochord distortions with the exception of MITC. Carbon disulfide (CS(2)), a common DTC degradate, also caused distortions at concentrations >200 times the DTCs. Whole mount in situ hybridization of developmental markers for collagen (collagen2a1), muscle (myoD), and body axis formation (no tail) was perturbed well after cessation of treatment with pyrolidine-DTC (PDTC), dimethyl-DTC (DMDTC), NaM, MITC, and CS(2). Therefore, distinct albeit related chemical classes share a common toxic effect on zebrafish notochord development. To test the responsiveness of the distortion to metal perturbation, five metal chelators and 2 metals were studied. The membrane permeable copper chelator neocuproine (NCu) was found to cause notochord distortions similar to DTC-related molecules. DMDTC and NCu treated animals were protected with copper, and collagen 2a1 and no tail gene expression patterns were identical to controls in these animals. PDTC, NaM, MITC, and CS(2) were not responsive to copper indicating that the chelation of metals is not the primary means by which these molecules elicit their developmental toxicity. Embryos treated with DMDTC, NaM, and NCu were rescued by adding triciaine (MS-222) which abolishes the spontaneous muscle contractions that begin at 18 hpf. In these animals, only collagen 2a1 expression showed a similar pattern to the other notochord distorting molecules. This indicates that the perturbation of no tail expression is in response to the muscle contractions distorting the notochord, while collagen 2a1 is associated with the impact of these molecules on much earlier developmental processes.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Aminobenzoic Acids, http://linkedlifedata.com/resource/pubmed/chemical/COL2A1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Carbon Disulfide, http://linkedlifedata.com/resource/pubmed/chemical/Chelating Agents, http://linkedlifedata.com/resource/pubmed/chemical/Collagen Type II, http://linkedlifedata.com/resource/pubmed/chemical/Copper, http://linkedlifedata.com/resource/pubmed/chemical/Dimethyldithiocarbamate, http://linkedlifedata.com/resource/pubmed/chemical/Disulfiram, http://linkedlifedata.com/resource/pubmed/chemical/Isothiocyanates, http://linkedlifedata.com/resource/pubmed/chemical/Phenanthrolines, http://linkedlifedata.com/resource/pubmed/chemical/Pyrrolidines, http://linkedlifedata.com/resource/pubmed/chemical/T-Box Domain Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Thiocarbamates, http://linkedlifedata.com/resource/pubmed/chemical/Zebrafish Proteins, http://linkedlifedata.com/resource/pubmed/chemical/ferbam, http://linkedlifedata.com/resource/pubmed/chemical/neocuproine, http://linkedlifedata.com/resource/pubmed/chemical/ntl protein, zebrafish, http://linkedlifedata.com/resource/pubmed/chemical/tricaine
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0041-008X
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
216
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
55-68
pubmed:dateRevised
2007-12-3
pubmed:meshHeading
pubmed-meshheading:16797628-Aminobenzoic Acids, pubmed-meshheading:16797628-Analysis of Variance, pubmed-meshheading:16797628-Animals, pubmed-meshheading:16797628-Body Patterning, pubmed-meshheading:16797628-Carbon Disulfide, pubmed-meshheading:16797628-Chelating Agents, pubmed-meshheading:16797628-Collagen Type II, pubmed-meshheading:16797628-Copper, pubmed-meshheading:16797628-Dimethyldithiocarbamate, pubmed-meshheading:16797628-Disulfiram, pubmed-meshheading:16797628-Dose-Response Relationship, Drug, pubmed-meshheading:16797628-Embryo, Nonmammalian, pubmed-meshheading:16797628-Gene Expression Regulation, Developmental, pubmed-meshheading:16797628-In Situ Hybridization, pubmed-meshheading:16797628-Isothiocyanates, pubmed-meshheading:16797628-Molecular Structure, pubmed-meshheading:16797628-Notochord, pubmed-meshheading:16797628-Phenanthrolines, pubmed-meshheading:16797628-Pyrrolidines, pubmed-meshheading:16797628-T-Box Domain Proteins, pubmed-meshheading:16797628-Thiocarbamates, pubmed-meshheading:16797628-Toxicity Tests, pubmed-meshheading:16797628-Zebrafish, pubmed-meshheading:16797628-Zebrafish Proteins
pubmed:year
2006
pubmed:articleTitle
Dithiocarbamates have a common toxic effect on zebrafish body axis formation.
pubmed:affiliation
Department of Environmental and Molecular Toxicology, Environmental Health Sciences Center and the Marine and Freshwater Biomedical Sciences Center, Oregon State University, Corvallis, OR 97331, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural