High intrinsic oxidative stress may underlie selective vulnerability of the hippocampal CA1 region

Oxidative stress (OS) causes extensive cell death in the CA1 but not the CA3 region of the hippocampus. We found that the CA1 region of hippocampus explants, cultured under normal conditions, had significantly higher superoxide levels and expressed both anti-oxidant genes and genes related to the ge...

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Published inBrain research. Molecular brain research. Vol. 140; no. 1; pp. 120 - 126
Main Authors Wang, Xinkun, Pal, Ranu, Chen, Xue-wen, Limpeanchob, Nanteetip, Kumar, Keshava N., Michaelis, Elias K.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 31.10.2005
Elsevier
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Online AccessGet full text
ISSN0169-328X
1872-6941
DOI10.1016/j.molbrainres.2005.07.018

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Abstract Oxidative stress (OS) causes extensive cell death in the CA1 but not the CA3 region of the hippocampus. We found that the CA1 region of hippocampus explants, cultured under normal conditions, had significantly higher superoxide levels and expressed both anti-oxidant genes and genes related to the generation of reactive oxygen species at significantly higher levels than the CA3. These observations were indicative of high intrinsic OS in CA1.
AbstractList Oxidative stress (OS) causes extensive cell death in the CA1 but not the CA3 region of the hippocampus. We found that the CA1 region of hippocampus explants, cultured under normal conditions, had significantly higher superoxide levels and expressed both anti-oxidant genes and genes related to the generation of reactive oxygen species at significantly higher levels than the CA3. These observations were indicative of high intrinsic OS in CA1.
Oxidative stress (OS) causes extensive cell death in the CA1 but not the CA3 region of the hippocampus. We found that the CA1 region of hippocampus explants, cultured under normal conditions, had significantly higher superoxide levels and expressed both anti-oxidant genes and genes related to the generation of reactive oxygen species at significantly higher levels than the CA3. These observations were indicative of high intrinsic OS in CA1.Oxidative stress (OS) causes extensive cell death in the CA1 but not the CA3 region of the hippocampus. We found that the CA1 region of hippocampus explants, cultured under normal conditions, had significantly higher superoxide levels and expressed both anti-oxidant genes and genes related to the generation of reactive oxygen species at significantly higher levels than the CA3. These observations were indicative of high intrinsic OS in CA1.
Author Wang, Xinkun
Pal, Ranu
Chen, Xue-wen
Kumar, Keshava N.
Limpeanchob, Nanteetip
Michaelis, Elias K.
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  givenname: Xinkun
  surname: Wang
  fullname: Wang, Xinkun
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  givenname: Xue-wen
  surname: Chen
  fullname: Chen, Xue-wen
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  givenname: Nanteetip
  surname: Limpeanchob
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  givenname: Keshava N.
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  givenname: Elias K.
  surname: Michaelis
  fullname: Michaelis, Elias K.
  email: emichaelis@ku.edu
  organization: Center for Neurobiology and Immunology Research, Higuchi Biosciences Center, 2099 Constant Avenue, The University of Kansas, Lawrence, KS 66047, USA
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Issue 1
Keywords DHE
Disorders of the nervous system
Oxidative stress
ALS
DQ
CA1
CA3
Nrf2
Nf1
Selective vulnerability
GST12-12
UGT1A6
Nqo1
Txnrd1/2
AD
NFκB
OS
GST1
MAPK
γ-ECS
ARE
PD
ROS
PI
Hippocampus
Central nervous system
CAI
Encephalon
Language English
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Snippet Oxidative stress (OS) causes extensive cell death in the CA1 but not the CA3 region of the hippocampus. We found that the CA1 region of hippocampus explants,...
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SubjectTerms Animals
Antioxidants - metabolism
Biological and medical sciences
CA1
CA3
Cells, Cultured
Fundamental and applied biological sciences. Psychology
Hippocampus
Hippocampus - cytology
Hippocampus - physiology
Male
Nrf2
Organ Culture Techniques
Oxidative stress
Oxidative Stress - physiology
Pyramidal Cells - chemistry
Pyramidal Cells - physiology
Rats
Rats, Sprague-Dawley
Selective vulnerability
Superoxides - metabolism
Vertebrates: nervous system and sense organs
Title High intrinsic oxidative stress may underlie selective vulnerability of the hippocampal CA1 region
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0169328X05002986
https://dx.doi.org/10.1016/j.molbrainres.2005.07.018
https://www.ncbi.nlm.nih.gov/pubmed/16137784
https://www.proquest.com/docview/17406432
https://www.proquest.com/docview/68691298
Volume 140
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