51. Reduction of ischemia-induced cerebral injury by all-trans-retinoic acid
- Author
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Sun-Yong Baek, Ji-Hoon Kim, Myoung-Eun Han, Young-Suk Lee, Jae-Bong Kim, Sae-Ock Oh, Bong-Seon Kim, Jong-Soo Jung, and Byung-Kwan Choi
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Male ,Photomicrography ,medicine.medical_specialty ,Blotting, Western ,Interleukin-1beta ,Anti-Inflammatory Agents ,Retinoic acid ,Ischemia ,Tretinoin ,Inflammation ,Pharmacology ,CCAAT-Enhancer-Binding Protein-beta ,Brain Ischemia ,Rats, Sprague-Dawley ,Brain ischemia ,chemistry.chemical_compound ,Enhancer binding ,medicine ,Animals ,Neurons ,Analysis of Variance ,Microscopy, Confocal ,Reverse Transcriptase Polymerase Chain Reaction ,business.industry ,General Neuroscience ,Brain ,Ectodysplasins ,medicine.disease ,Immunohistochemistry ,Rats ,Surgery ,chemistry ,Cyclooxygenase 2 ,medicine.symptom ,business ,medicine.drug - Abstract
Ischemia-induced cerebral injury evolves over a longer period than previously believed through post-ischemic inflammation. Retinoic acid (RA) has been shown to exert cytoprotective effects on several cells, but its effects on ischemia-induced cerebral injury have been poorly characterized. The aim of the present study was to examine the effects of all-trans-RA on ischemia-induced cerebral injury and elucidate the underlying mechanism. All-trans-RA treatment reduced the size of the ischemia-induced cerebral infarct. To elucidate the underlying mechanism, ischemia-induced cerebral inflammation was studied by examination of expressions of interleukin 1beta (IL-1beta) and ED-1. RA treatment significantly reduced the cerebral inflammation. Moreover, cerebral ischemic induction of cyclooxygenase-2 (COX-2) and CCAAT/enhancer binding protein beta (C/EBPbeta), which binds to the COX-2 promoter, was also inhibited by RA. These results suggest that RA can reduce ischemia-induced cerebral injury by an anti-inflammatory action, which may be effected via inhibition of C/EBPbeta-mediated COX-2 induction.
- Published
- 2008
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