Mild cerebral hypoxia-ischemia produces a sub-acute transient inflammatory response that is less selective and prolonged after a substantial insult

International Journal of Developmental Neuroscience

Volumn 27, Issue 7, 2009, Pages 691-700

  Qiao, Min ^a   Meng, Shuzhen ^b,c   Foniok, Tadeusz ^a   Tuor, Ursula I ^a,b  

^a NATIONAL RESEARCH COUNCIL CANADA   (Canada)

^b UNIVERSITY OF CALGARY   (Canada)

^c CHINA MEDICAL UNIVERSITY   (China)

Author keywords

Cell death; Cerebral hypoxia ischemia; Inflammation; Microglial activation; Neonatal; White matter

Indexed keywords

3 NITROTYROSINE; BIOLOGICAL MARKER; CYTOKINE; MYELIN; NITRIC OXIDE; TUMOR NECROSIS FACTOR ALPHA;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN ATROPHY; BRAIN CORTEX; BRAIN DAMAGE; BRAIN HYPOXIA; BRAIN INJURY; BRAIN ISCHEMIA; BRAIN NECROSIS; CELL ACTIVATION; CONTROLLED STUDY; CYTOKINE RELEASE; DISEASE SEVERITY; GRAY MATTER; IN VIVO STUDY; INFLAMMATION; MACROPHAGE ACTIVATION; MICROGLIA; MONITORING; NERVE CELL NECROSIS; NERVE FIBER; NEUROIMAGING; NITROSATIVE STRESS; NONHUMAN; PRIORITY JOURNAL; RAT; WHITE MATTER;

ANIMALS; BRAIN; CELL DEATH; GLIAL FIBRILLARY ACIDIC PROTEIN; HYPOXIA-ISCHEMIA, BRAIN; INFLAMMATION; MYELIN BASIC PROTEINS; RANDOM ALLOCATION; RATS; TUMOR NECROSIS FACTOR-ALPHA; TYROSINE;

EID: 70349329243     PISSN: 07365748     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijdevneu.2009.07.004     Document Type: Article

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