1996•PubMedRequires access

[Identification of neuronal death and DNA fragmentation in early stage after rat transient forebrain ischemia].

Shoji Kazahari, Shin‐ya Takizawa, Satoshi Ogawa, Sonoko Habu, Yasuro Shinohara

Open publisher page 2 citations

Abstract

To clarify whether programmed cell death plays an important role in the delayed neuronal death after forebrain transient ischemia, we investigated the relationship between pathological changes visualized by HE staining and intranuclear DNA fragmentation evaluated by the TUNEL method in rat hippocampal CA1 pyramidal neurons at early times after the onset of transient forebrain ischemia. The investigations were carried out in male Wistar rats (N = 22) subjected to 20 minutes of transient forebrain ischemia by Pulsinelli's method. No morphological changes or TUNEL staining were observed at 1 hour after forebrain ischemia. HE staining revealed morphological changes in 8 +/- 4%, 10 +/- 4% and 88 +/- 9% of neurons in hippocampus CA1 at 3, 6 and 24 hours after forebrain ischemia, respectively at which times 0%, 74 +/- 1% and 68 +/- 11% of the neurons showed marked labeling with the TUNEL method. We therefore conclude that DNA fragmentation as evaluated by the TUNEL method is not involved in neuronal death, and no DNA fragmentation was detectable prior to morphological changes in the early stage of forebrain ischemia.

About this research paper

What this paper is about

To clarify whether programmed cell death plays an important role in the delayed neuronal death after forebrain transient ischemia, we investigated the relationship between pathological changes visualized by HE staining and intranuclear DNA fragmentation evaluated by the TUNEL method in rat hippocampal CA1 pyramidal neurons at early times after the onset of transient forebrain ischemia. The investigations were carried out in male Wistar rats (N = 22) subjected to 20 minutes of transient forebrain ischemia by Pulsinelli's method. No morphological changes or TUNEL staining were observed at 1 hour after forebrain ischemia. HE staining revealed morphological changes in 8 +/- 4%, 10 +/- 4% and 88 +/- 9% of neurons in hippocampus CA1 at 3, 6 and 24 hours after forebrain ischemia, respectively at which times 0%, 74 +/- 1% and 68 +/- 11% of the neurons showed marked labeling with the TUNEL method. We therefore conclude that DNA fragmentation as evaluated by the TUNEL method is not involved in neuronal death, and no DNA fragmentation was detectable prior to morphological changes in the early stage of forebrain ischemia.

Why it matters

OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

To clarify whether programmed cell death plays an important role in the delayed neuronal death after forebrain transient ischemia, we investigated the relationship between pathological changes visualized by HE staining and intranuclear DNA fragmentation evaluated by the TUNEL method in rat hippocampal CA1 pyramidal neurons at early times after the onset of transient forebrain ischemia. The investigations were carried out in male Wistar rats (N = 22) subjected to 20 minutes of transient forebrain ischemia by Pulsinelli's method. No morphological changes or TUNEL staining were observed at 1 hour after forebrain ischemia. HE staining revealed morphological changes in 8 +/- 4%, 10 +/- 4% and 88 +/- 9% of neurons in hippocampus CA1 at 3, 6 and 24 hours after forebrain ischemia, respectively at which times 0%, 74 +/- 1% and 68 +/- 11% of the neurons showed marked labeling with the TUNEL method. We therefore conclude that DNA fragmentation as evaluated by the TUNEL method is not involved in neuronal death, and no DNA fragmentation was detectable prior to morphological changes in the early stage of forebrain ischemia.

Key concepts: TUNEL assay, Forebrain, DNA fragmentation, Hippocampal formation, Fragmentation (computing), Ischemia, Hippocampus, Programmed cell death

Related papers

Back to paper searchBrowse research topicsOriginal source
[Identification of neuronal death and DNA fragmentation in early stage after rat transient forebrain ischemia]. — Research Paper | ScholarLens