Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1999-3-30
pubmed:abstractText
This study was performed to examine the involvement of apoptosis and the expression of bcl-2 family genes in ischemia-induced retinal injury. Retinal ischemia was induced in adult rats by raising the intraocular pressure to 130 mmHg for 45 min. Selective damage to the inner retina was observed 7 days after ischemia. No terminal deoxynucleotidyl-transferase (TdT)-mediated dUTP nick end-labeling (TUNEL) positive cells were observed in the normal retina, but there was a significant number of TUNEL positive cells 6-48 h after transient ischemia followed by a decrease at 96 and 168 h. The number of TUNEL positive cells reached a maximum at 24 h after ischemia. DNA laddering was observed on agarose gel electrophoresis with the retinas 24 and 48 h after ischemia but not in the normal retina. Semiquantitative reverse transcription-polymerase chain reaction (RT-PCR) revealed that bax gene expression did not change immediately after cessation of ischemia, but gradually increased as early as 6 h, reached a peak at 24 h, then decreased to near baseline levels at 168 h. On the other hand, bcl-2 gene expression showed no obvious changes at any time after transient ischemia. Moreover, intense Bax protein immunoreactivity was detected in the retinal sections at 24 h after ischemia although little immunoreactivity was present in the normal sections. These results suggest that apoptosis associated with the expression of Bax is involved in retinal cell loss after ischemic insult.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0006-8993
pubmed:author
pubmed:issnType
Print
pubmed:day
2
pubmed:volume
815
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
11-20
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:9974117-Animals, pubmed-meshheading:9974117-Apoptosis, pubmed-meshheading:9974117-Brain Chemistry, pubmed-meshheading:9974117-DNA Fragmentation, pubmed-meshheading:9974117-Electrophoresis, pubmed-meshheading:9974117-Gene Expression, pubmed-meshheading:9974117-Immunohistochemistry, pubmed-meshheading:9974117-In Situ Nick-End Labeling, pubmed-meshheading:9974117-Ischemic Attack, Transient, pubmed-meshheading:9974117-Male, pubmed-meshheading:9974117-Neurons, pubmed-meshheading:9974117-Proto-Oncogene Proteins, pubmed-meshheading:9974117-Proto-Oncogene Proteins c-bcl-2, pubmed-meshheading:9974117-RNA, Messenger, pubmed-meshheading:9974117-Rats, pubmed-meshheading:9974117-Rats, Sprague-Dawley, pubmed-meshheading:9974117-Reperfusion Injury, pubmed-meshheading:9974117-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:9974117-bcl-2-Associated X Protein
pubmed:year
1999
pubmed:articleTitle
Apoptotic DNA fragmentation and upregulation of Bax induced by transient ischemia of the rat retina.
pubmed:affiliation
Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Kyoto University, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't