Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2003-9-26
pubmed:abstractText
It is in dispute whether caspase 3 contributes to status epilepticus (SE)-induced cell loss. We hypothesized that caspase 3-mediated cell death continues beyond the acute phase of SE. We induced SE with either kainic acid or electrical stimulation of the amygdala in Wistar and Sprague-Dawley rats. Caspase 3 immunohistochemistry, Western blot analysis and enzyme activity measurements were used to determine cellular localization and the time course of caspase 3 expression and activation. Immunohistochemistry indicated that caspase 3 protein expression increased following SE, peaking at 16-24 h. Cleavage of procaspase 3 to active fragments (p20-17) was detected 2-7 days after SE. Caspase 3 enzyme activity was elevated at 8 h and further increased up to 19.4-fold at 7 days following SE. Activation of caspase 3 after SE occurred in the hippocampus and the extrahippocampal temporal lobe but not in the thalamus. Caspase 3-immunoreactive cells represented only a minority of degenerating cells as assessed by Fluoro-Jade B and TUNEL staining. Analysis of double-labelled sections indicated that active caspase 3 was located in astrocytes rather than neurons or microglia. There was increased caspase 3 expression in both rat strains, and it was independent of the method used to induce SE. These data demonstrate that caspase 3 contributes to the cell death occurring within the first week after SE, but in only a small proportion of degenerating cells. These results suggest that, contrary to expectations, caspase 3 inhibitors would have only limited benefits in the treatment of SE.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Casp3 protein, rat, http://linkedlifedata.com/resource/pubmed/chemical/Caspase 3, http://linkedlifedata.com/resource/pubmed/chemical/Caspases, http://linkedlifedata.com/resource/pubmed/chemical/DEVDase, http://linkedlifedata.com/resource/pubmed/chemical/Excitatory Amino Acid Agonists, http://linkedlifedata.com/resource/pubmed/chemical/Fluorescent Dyes, http://linkedlifedata.com/resource/pubmed/chemical/Glial Fibrillary Acidic Protein, http://linkedlifedata.com/resource/pubmed/chemical/Kainic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Organic Chemicals, http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments, http://linkedlifedata.com/resource/pubmed/chemical/Peptide Hydrolases, http://linkedlifedata.com/resource/pubmed/chemical/Phosphopyruvate Hydratase, http://linkedlifedata.com/resource/pubmed/chemical/fluoro jade
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0953-816X
pubmed:author
pubmed:issnType
Print
pubmed:volume
18
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1486-96
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:14511328-Animals, pubmed-meshheading:14511328-Blotting, Western, pubmed-meshheading:14511328-Brain, pubmed-meshheading:14511328-Caspase 3, pubmed-meshheading:14511328-Caspases, pubmed-meshheading:14511328-Cell Count, pubmed-meshheading:14511328-Cell Death, pubmed-meshheading:14511328-Disease Models, Animal, pubmed-meshheading:14511328-Electric Stimulation, pubmed-meshheading:14511328-Enzyme Activation, pubmed-meshheading:14511328-Excitatory Amino Acid Agonists, pubmed-meshheading:14511328-Fluorescent Dyes, pubmed-meshheading:14511328-Glial Fibrillary Acidic Protein, pubmed-meshheading:14511328-Immunohistochemistry, pubmed-meshheading:14511328-In Situ Nick-End Labeling, pubmed-meshheading:14511328-Kainic Acid, pubmed-meshheading:14511328-Male, pubmed-meshheading:14511328-Neuroglia, pubmed-meshheading:14511328-Organic Chemicals, pubmed-meshheading:14511328-Peptide Fragments, pubmed-meshheading:14511328-Peptide Hydrolases, pubmed-meshheading:14511328-Phosphopyruvate Hydratase, pubmed-meshheading:14511328-Rats, pubmed-meshheading:14511328-Rats, Sprague-Dawley, pubmed-meshheading:14511328-Status Epilepticus, pubmed-meshheading:14511328-Time Factors
pubmed:year
2003
pubmed:articleTitle
Expression and activation of caspase 3 following status epilepticus in the rat.
pubmed:affiliation
A.I. Virtanen Institute for Molecular Sciences, University of Kuopio, PO Box 1627, FIN-70 211 Kuopio, Finland.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't