Single-strand DNA damages and its relationship with morphological change of neurons at early stage of rat cerebral ischemia/reperf usion
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Single-strand DNA damages and its relationship with morphological change of neurons at early stage of rat cerebral ischemia/reperf usion
Single-strand DNA damages and its relationship with morphological change of neurons at early stage of rat cerebral ischemia/reperf usion
解放军医学杂志(英文版)2002年第4期 页码:270-275
Affiliations:
1. Department of Neurology
2. Xijing Hospital
3. Fourth Military Medical University
4. ,China
Author bio:
Funds:
DOI:
中图分类号:R741
纸质出版:2002
Accepted:
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Single-strand DNA damages and its relationship with morphological change of neurons at early stage of rat cerebral ischemia/reperf usion[J]. 解放军医学杂志(英文版), 2002,(4):270-275.
[1]张巍,万琪,刘勇红.Single-strand DNA damages and its relationship with morphological change of neurons at early stage of rat cerebral ischemia/reperf usion[J].Journal of Medical Colleges of PLA,2002(04):270-275.
Single-strand DNA damages and its relationship with morphological change of neurons at early stage of rat cerebral ischemia/reperf usion[J]. 解放军医学杂志(英文版), 2002,(4):270-275.DOI:
[1]张巍,万琪,刘勇红.Single-strand DNA damages and its relationship with morphological change of neurons at early stage of rat cerebral ischemia/reperf usion[J].Journal of Medical Colleges of PLA,2002(04):270-275.DOI:
Single-strand DNA damages and its relationship with morphological change of neurons at early stage of rat cerebral ischemia/reperf usion
摘要
Abstract
<正> Objective: To discuss the DNA-strand breaks at early stage of middle cerebral artery occlusion/ reperfusion (MCAO/R). Methods: Neurons number and morphologic change were observed by Nissl stain method
and DNA strand breaks were in situ detected by using DNA polymerase- I Klenow fragment-mediated nick end-labelling method (Klenow method). Results: Six hours after reperfusion
a few neurons in damaged regions appeared morphologic changes while a few Klenow-positive cells were detected (P<0. 01). Twenty-four hours after reperfusion lots of neurons showed morphologic change while the number of Klenow-positive cells immediately and remarkably increased (P<0. 01). Seventy-two hours after reperfusion the number of neurons decreased significantly and the number of Klenow-positive cells was also less than that in 24 h (P<0. 05). Conclusion: ① 24 h after reperfusion when the number of Klenow-positive cells reached peak value
DNA single-strand breaks (SSBs) took place in many Klenow-positive cells
and presumed
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