Literature DB >> 21382467

Spatial and temporal patterns of oxidative stress in the brain of gerbils submitted to different duration of global cerebral ischemia.

Vesna Selakovic1, Andrej Korenic, Lidija Radenovic.   

Abstract

The present study was undertaken to examine spatial and temporal patterns of oxidative stress rate in the brain of Mongolian gerbils submitted to different duration of global ischemia/reperfusion. The common carotid arteries of gerbils were occluded for 5, 10, or 15 min. We followed the temporal ischemia-induced oxidative stress rate, the most important factor that exacerbates brain damage by reperfusion, starting from 24 h up to 28 days after reperfusion. The spatial ischemia-induced oxidative stress distribution was measured parallely in different brain regions: forebrain cortex, striatum, hippocampus and cerebellum. Post-ischemic effects were followed in vivo by monitoring the neurological status of whole animals and at the intracellular level by standard biochemical assays in different brain regions. We measured superoxide production, superoxide dismutase activity, nitric oxide production, index of lipid peroxidation, and reduced glutathione. Our results revealed a pattern of dynamic changes in each oxidative stress parameter that corresponded with ischemia duration in all tested brain structures. The highest levels were obtained in the first 24h after the insult. After that, they slowly returned to nearly control values 28 days after reperfusion (with the exception of SOD activity that returned to control values at fourth day after reperfusion). The most sensitive oxidative stress parameter was index of lipid peroxidation. Our study confirmed spatial distribution of ischemia-induced oxidative stress. Tested brain structures showed different sensitivity to each oxidative stress parameter, although their basal levels were similar. These new findings could be valuable for creation and strategy of post-ischemic therapy.
Copyright © 2011 ISDN. Published by Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21382467     DOI: 10.1016/j.ijdevneu.2011.02.009

Source DB:  PubMed          Journal:  Int J Dev Neurosci        ISSN: 0736-5748            Impact factor:   2.457


  14 in total

1.  The oxygen free radicals originating from mitochondrial complex I contribute to oxidative brain injury following hypoxia-ischemia in neonatal mice.

Authors:  Zoya V Niatsetskaya; Sergei A Sosunov; Dzmitry Matsiukevich; Irina V Utkina-Sosunova; Veniamin I Ratner; Anatoly A Starkov; Vadim S Ten
Journal:  J Neurosci       Date:  2012-02-29       Impact factor: 6.167

2.  Neuroprotection of Ischemic Preconditioning is Mediated by Anti-inflammatory, Not Pro-inflammatory, Cytokines in the Gerbil Hippocampus Induced by a Subsequent Lethal Transient Cerebral Ischemia.

Authors:  Dong Won Kim; Jae-Chul Lee; Jeong-Hwi Cho; Joon Ha Park; Ji Hyeon Ahn; Bai Hui Chen; Bich-Na Shin; Hyun-Jin Tae; Jeong Yeol Seo; Jun Hwi Cho; Il Jun Kang; Seongkweon Hong; Young-Myeong Kim; Moo-Ho Won; In Hye Kim
Journal:  Neurochem Res       Date:  2015-08-20       Impact factor: 3.996

3.  Eventual analysis of global cerebral ischemia-reperfusion injury in rat brain: a paradigm of a shift in stress and its influence on cognitive functions.

Authors:  Sriram Ravindran; Gino A Kurian
Journal:  Cell Stress Chaperones       Date:  2019-04-25       Impact factor: 3.667

4.  The Zinc Ion Chelating Agent TPEN Attenuates Neuronal Death/apoptosis Caused by Hypoxia/ischemia Via Mediating the Pathophysiological Cascade Including Excitotoxicity, Oxidative Stress, and Inflammation.

Authors:  Wei-Ming Wang; Zhao Liu; Ai-Jun Liu; Yu-Xiang Wang; Hong-Gang Wang; Di An; Bin Heng; Lai-Hua Xie; Jun-Li Duan; Yan-Qiang Liu
Journal:  CNS Neurosci Ther       Date:  2015-07-20       Impact factor: 5.243

5.  Neuronal damage using fluoro-Jade B histofluorescence and gliosis in the gerbil septum submitted to various durations of cerebral ischemia.

Authors:  Chan Woo Park; Jae-Chul Lee; Ji Hyeon Ahn; Dae Hwan Lee; Geum-Sil Cho; Bing Chun Yan; Joon Ha Park; In Hye Kim; Hui Young Lee; Moo-Ho Won; Jun Hwi Cho
Journal:  Cell Mol Neurobiol       Date:  2013-07-28       Impact factor: 5.046

6.  Brain ischemic preconditioning protects against moderate, not severe, transient global cerebral ischemic injury.

Authors:  Jae-Chul Lee; Bich-Na Shin; Jeong Hwi Cho; Tae-Kyeong Lee; In Hye Kim; YooHun Noh; Sung-Su Kim; Hyang-Ah Lee; Young-Myeong Kim; Hyeyoung Kim; Jun Hwi Cho; Joon Ha Park; Ji Hyeon Ahn; Il Jun Kang; In Koo Hwang; Moo-Ho Won; Myoung Cheol Shin
Journal:  Metab Brain Dis       Date:  2018-04-12       Impact factor: 3.584

Review 7.  Caffeine and Its Neuroprotective Role in Ischemic Events: A Mechanism Dependent on Adenosine Receptors.

Authors:  R Brito; K C Calaza; D Pereira-Figueiredo; A A Nascimento; M C Cunha-Rodrigues
Journal:  Cell Mol Neurobiol       Date:  2021-03-17       Impact factor: 5.046

8.  Effect of ischemic preconditioning on the expression of c-myb in the CA1 region of the gerbil hippocampus after ischemia/reperfusion injury.

Authors:  Hui Young Lee; Hyun-Jin Tae; Geum-Sil Cho; In Hye Kim; Jeong Hwi Cho; Joon Ha Park; Ji Hyeon Ahn; Bai Hui Chen; Bich-Na Shin; Moo-Ho Won; Chan Woo Park; Jun Hwi Cho; Jeong Yeol Seo; Jae-Chul Lee
Journal:  Iran J Basic Med Sci       Date:  2016-06       Impact factor: 2.699

9.  Linoleic acid participates in the response to ischemic brain injury through oxidized metabolites that regulate neurotransmission.

Authors:  Marie Hennebelle; Zhichao Zhang; Adam H Metherel; Alex P Kitson; Yurika Otoki; Christine E Richardson; Jun Yang; Kin Sing Stephen Lee; Bruce D Hammock; Liang Zhang; Richard P Bazinet; Ameer Y Taha
Journal:  Sci Rep       Date:  2017-06-28       Impact factor: 4.379

10.  Extremely low frequency magnetic field (50 Hz, 0.5 mT) reduces oxidative stress in the brain of gerbils submitted to global cerebral ischemia.

Authors:  Snežana Rauš Balind; Vesna Selaković; Lidija Radenović; Zlatko Prolić; Branka Janać
Journal:  PLoS One       Date:  2014-02-19       Impact factor: 3.240

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