1998
DOI: 10.1016/s0041-1345(98)00869-0
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Induction of immediate early genes and apoptosis after ischemia/reperfusion in fatty liver rats

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Cited by 8 publications
(5 citation statements)
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“…Recently, immediate early genes are thought to play an important role in the process of inducing apoptosis or the regeneration of various cells, and indeed, transcriptional activation of AP-1 family encoded by immediate early genes was observed in the I/R injured neurons [12], myocardium [13], kidney [14], and liver [15][16][17][18]. In a rat intestinal I/R injury model, apoptosis and regeneration of the IECs were observed after reperfusion [19,20].…”
Section: Discussionmentioning
confidence: 99%
“…Recently, immediate early genes are thought to play an important role in the process of inducing apoptosis or the regeneration of various cells, and indeed, transcriptional activation of AP-1 family encoded by immediate early genes was observed in the I/R injured neurons [12], myocardium [13], kidney [14], and liver [15][16][17][18]. In a rat intestinal I/R injury model, apoptosis and regeneration of the IECs were observed after reperfusion [19,20].…”
Section: Discussionmentioning
confidence: 99%
“…The induction of apoptosis may correlate with the severity of tissue ischemic damage. We have previously reported that enhanced and persistent expression of IEGs was associated with severe injury and poor survival in experimental animals subjected to hepatic I‐R, liver transplantation, or hemorrhagic shock 8,18,19. Thus, it is reasonable to assume that IPC may lead to a reduction in IEG expression, which, subsequently, results in significant reduction of apoptosis after I‐R.…”
Section: Discussionmentioning
confidence: 99%
“…Preparation of total RNA and Northern blot analysis were carried out as described previously 8,18,19. Total RNA was extracted from the frozen liver specimen with Isogen (Amersham, Sydney, Australia) and the liquid was size‐fractionated by 1% (w/v) agaroseformaldehyde gel electrophoresis, transferred onto Hybond‐N nylon membranes (Amersham) by capillary transfer, using 10 × SSC (1 × SSC = 0.15 M NaCl, and 0.015 M sodium citrate), and baked for 2 h and 80°C.…”
Section: Methodsmentioning
confidence: 99%
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