Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1998-10-14
pubmed:abstractText
To clarify mechanisms of neuronal death in the postischemic brain, we examined whether astrocytes exposed to hypoxia/reoxygenation exert a neurotoxic effect, using a coculture system. Neurons cocultured with astrocytes subjected to hypoxia/reoxygenation underwent apoptotic cell death, the effect enhanced by a combination of interleukin-1beta with hypoxia. The synergistic neurotoxic activity of hypoxia and interleukin-1beta was dependent on de novo expression of inducible nitric oxide synthase (iNOS) and on nitric oxide (NO) production in astrocytes. Further analysis to determine the neurotoxic mechanism revealed decreased Bcl-2 and increased Bax expression together with caspase-3 activation in cortical neurons cocultured with NO-producing astrocytes. Inhibition of NO production in astrocytes by N(G)-monomethyl-L-arginine, an inhibitor of NOS, significantly inhibited neuronal death together with changes in Bcl-2 and Bax protein levels and in caspase-3-like activity. Moreover, treatment of neurons with a bax antisense oligonucleotide inhibited the caspase-3-like activation and neuronal death induced by an NO donor, sodium nitroprusside. These data suggest that NO produced by astrocytes after hypoxic insult induces apoptotic death of neurons through mechanisms involving the caspase-3 activation after down-regulation of Bcl-2 and up-regulation of Bax protein levels.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Bax protein, rat, 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/Cysteine Endopeptidases, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase Type II, http://linkedlifedata.com/resource/pubmed/chemical/Nos2 protein, rat, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-bcl-2, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/bcl-2-Associated X Protein
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0022-3042
pubmed:author
pubmed:issnType
Print
pubmed:volume
71
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1588-96
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:9751192-Animals, pubmed-meshheading:9751192-Apoptosis, pubmed-meshheading:9751192-Astrocytes, pubmed-meshheading:9751192-Caspase 3, pubmed-meshheading:9751192-Caspases, pubmed-meshheading:9751192-Cell Hypoxia, pubmed-meshheading:9751192-Cell Survival, pubmed-meshheading:9751192-Cells, Cultured, pubmed-meshheading:9751192-Coculture Techniques, pubmed-meshheading:9751192-Cysteine Endopeptidases, pubmed-meshheading:9751192-Enzyme Activation, pubmed-meshheading:9751192-Enzyme Induction, pubmed-meshheading:9751192-Interleukin-1, pubmed-meshheading:9751192-Multigene Family, pubmed-meshheading:9751192-Neurons, pubmed-meshheading:9751192-Nitric Oxide, pubmed-meshheading:9751192-Nitric Oxide Synthase, pubmed-meshheading:9751192-Nitric Oxide Synthase Type II, pubmed-meshheading:9751192-Proto-Oncogene Proteins, pubmed-meshheading:9751192-Proto-Oncogene Proteins c-bcl-2, pubmed-meshheading:9751192-RNA, Messenger, pubmed-meshheading:9751192-Rats, pubmed-meshheading:9751192-Rats, Sprague-Dawley, pubmed-meshheading:9751192-bcl-2-Associated X Protein
pubmed:year
1998
pubmed:articleTitle
Involvement of Bcl-2 family and caspase-3-like protease in NO-mediated neuronal apoptosis.
pubmed:affiliation
Department of Anatomy and Neuroscience, Osaka University Medical School, Suita, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't