2007
DOI: 10.1007/s10735-007-9102-9
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Immunohistochemical changes in vulnerable rat brain regions after reversible global brain ischaemia

Abstract: Human global ischaemia was simulated in adult rats by inducing 20 min brain ischaemia and 60 min post-ischaemic recirculation. Immunohistochemical expression of MMP-9, TIMP-3, Bax and Bcl-2, and DNA fragmentation (with the TUNEL reaction) were investigated. The morphological data showed different neuronal responses in the hippocampus compared with the cerebral and cerebellar cortices. MMP-9 immunoreactivity was different in the hippocampus, particularly in dentate gyrus and the CA1 region, compared with these … Show more

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Cited by 21 publications
(16 citation statements)
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“…As previously reported, an increase in neurogenesis following ischemia has been considered to be necessary for functional recovery after stroke [19,20] . Beclin1-dependent autophagy has been associated with neurogenesis in several models [21,22] .…”
Section: Introductionmentioning
confidence: 85%
“…As previously reported, an increase in neurogenesis following ischemia has been considered to be necessary for functional recovery after stroke [19,20] . Beclin1-dependent autophagy has been associated with neurogenesis in several models [21,22] .…”
Section: Introductionmentioning
confidence: 85%
“…In order to investigate their roles in regulating mitochondrial permeability, recent studies show functions of these proteins in control of mitochondrial fission and fusion [40]. The level of Bcl-2 protein decreases in brain ischemia [41] and overexpression of prosurvival proteins Bcl-2 family can compete against cerebral ischemia [42]. The neuroprotective mechanism involves maintaining mitochondrial function [43].…”
Section: Discussionmentioning
confidence: 99%
“…Neuronal apoptosis in the hippocampal CA1 region was assessed by TUNEL staining, using an in situ cell death detection kit (TMR green, Roche, Mannheim, Germany). The brain sections at 24 hours after reperfusion (sham, n=5; GCI, n=7; HTEA, n=5) were used to perform immunohistochemistry as described [27]. The primary antibodies were: rabbit polyclonal antibody against PARP (1:200, ab6079, Abcam), Bcl-2 (1:100, BA0412, Boster) or Bax (1:100, BA0315-1, Boster).…”
Section: Methodsmentioning
confidence: 99%