Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2008-3-17
pubmed:abstractText
Dichloroacetyl chloride (DCAC) is a reactive metabolite of trichloroethene (TCE). TCE and its metabolites have been implicated in the induction of organ-specific and systemic autoimmunity, in the acceleration of autoimmune responses, and in the development of liver toxicity and hepatocellular carcinoma. In humans, effects of environmental toxicants are often multifactorial and detected only after long-term exposure. Therefore, we developed a mouse model to determine mechanisms by which DCAC and related acylating agents affect the liver. Autoimmune-prone female MRL +/+ mice were injected intraperitoneally with 0.2 mmol/kg of DCAC or dichloroacetic anhydride (DCAA) in corn oil twice weekly for six weeks. No overt liver pathology was detectable. Using microarray gene expression analysis, we detected changes in the liver transcriptome consistent with inflammatory processes. Both acylating toxicants up-regulated the expression of acute phase response and inflammatory genes. Furthermore, metallothionein genes were strongly up-regulated, indicating effects of the toxicants on zinc ion homeostasis and stress responses. In addition, DCAC and DCAA induced the up-regulation of several genes indicative of tumorigenesis. Our data provide novel insight into early mechanisms for the induction of liver disease by acylating agents. The data also demonstrate the power of microarray analysis in detecting early changes in liver function following exposure to environmental toxicants.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0893-228X
pubmed:author
pubmed:issnType
Print
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
572-82
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:18293905-Acetic Acids, pubmed-meshheading:18293905-Acetic Anhydrides, pubmed-meshheading:18293905-Acylation, pubmed-meshheading:18293905-Animals, pubmed-meshheading:18293905-Biotin, pubmed-meshheading:18293905-Drug-Induced Liver Injury, pubmed-meshheading:18293905-Female, pubmed-meshheading:18293905-Gene Expression, pubmed-meshheading:18293905-Gene Expression Profiling, pubmed-meshheading:18293905-In Situ Hybridization, pubmed-meshheading:18293905-Inflammation, pubmed-meshheading:18293905-Liver Function Tests, pubmed-meshheading:18293905-Metallothionein, pubmed-meshheading:18293905-Mice, pubmed-meshheading:18293905-Mice, Inbred MRL lpr, pubmed-meshheading:18293905-Multigene Family, pubmed-meshheading:18293905-Oligonucleotide Array Sequence Analysis, pubmed-meshheading:18293905-RNA, pubmed-meshheading:18293905-RNA, Complementary
pubmed:year
2008
pubmed:articleTitle
Transcriptomic analysis reveals early signs of liver toxicity in female MRL +/+ mice exposed to the acylating chemicals dichloroacetyl chloride and dichloroacetic anhydride.
pubmed:affiliation
Department of Microbiology & Immunology, The University of Texas Medical Branch, Galveston, Texas 77555, USA. rokonig@utmb.edu
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural