The Cycloxygenase-2 inhibitor SC58236 is neuroprotective in an in vivo model of focal ischemia in the rat

Focal ischemia was induced in the fronto-parietal region of rat brain, by injection of Rose Bengal, followed by light activation. Focal ischemia was accompanied by formation of PGD 2 peaking 60–90 min post irradiation and declining thereafter. Increased Cycloxygenase-2 (COX-2) expression was also ob...

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Published inNeuroscience letters Vol. 303; no. 2; pp. 91 - 94
Main Authors Govoni, Stefano, Masoero, Elisabetta, Favalli, Luigia, Rozza, Annalinda, Scelsi, Roberto, Viappiani, Serena, Buccellati, Carola, Sala, Angelo, Folco, Giancarlo
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LanguageEnglish
Published Shannon Elsevier Ireland Ltd 04.05.2001
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Abstract Focal ischemia was induced in the fronto-parietal region of rat brain, by injection of Rose Bengal, followed by light activation. Focal ischemia was accompanied by formation of PGD 2 peaking 60–90 min post irradiation and declining thereafter. Increased Cycloxygenase-2 (COX-2) expression was also observed. Control ischemic rats showed distinct morphological alterations with necrosis of neurons, glial cells and blood vessels, surrounded by a halo with pyknotic cells with cytoplasm swelling and vacuolization. Compound SC58236, a selective COX-2 inhibitor, dose-dependently prevented, ischemia-induced eicosanoid formation (area under the curve (AUC) of controls: 3.11±0.87; AUC of 20 mg/kg SC58236: 0.39±0.24), and caused significant reduction of damaged area (30.7 and 18.9% at SC58236 20 and 6.6 mg/kg), suggesting that selective inhibitors of COX-2 are neuroprotective.
AbstractList Focal ischemia was induced in the fronto-parietal region of rat brain, by injection of Rose Bengal, followed by light activation. Focal ischemia was accompanied by formation of PGD(2) peaking 60-90 min post irradiation and declining thereafter. Increased Cycloxygenase-2 (COX-2) expression was also observed. Control ischemic rats showed distinct morphological alterations with necrosis of neurons, glial cells and blood vessels, surrounded by a halo with pyknotic cells with cytoplasm swelling and vacuolization. Compound SC58236, a selective COX-2 inhibitor, dose-dependently prevented, ischemia-induced eicosanoid formation (area under the curve (AUC) of controls: 3.11 +/- 0.87; AUC of 20 mg/kg SC58236: 0.39 +/- 0.24), and caused significant reduction of damaged area (30.7 and 18.9% at SC58236 20 and 6.6 mg/kg), suggesting that selective inhibitors of COX-2 are neuroprotective.
Focal ischemia was induced in the fronto-parietal region of rat brain, by injection of Rose Bengal, followed by light activation. Focal ischemia was accompanied by formation of PGD 2 peaking 60–90 min post irradiation and declining thereafter. Increased Cycloxygenase-2 (COX-2) expression was also observed. Control ischemic rats showed distinct morphological alterations with necrosis of neurons, glial cells and blood vessels, surrounded by a halo with pyknotic cells with cytoplasm swelling and vacuolization. Compound SC58236, a selective COX-2 inhibitor, dose-dependently prevented, ischemia-induced eicosanoid formation (area under the curve (AUC) of controls: 3.11±0.87; AUC of 20 mg/kg SC58236: 0.39±0.24), and caused significant reduction of damaged area (30.7 and 18.9% at SC58236 20 and 6.6 mg/kg), suggesting that selective inhibitors of COX-2 are neuroprotective.
Focal ischemia was induced in the fronto-parietal region of rat brain, by injection of Rose Bengal, followed by light activation. Focal ischemia was accompanied by formation of PGD sub(2) peaking 60-90 min post irradiation and declining thereafter. Increased Cycloxygenase-2 (COX-2) expression was also observed. Control ischemic rats showed distinct morphological alterations with necrosis of neurons, glial cells and blood vessels, surrounded by a halo with pyknotic cells with cytoplasm swelling and vacuolization. Compound SC58236, a selective COX-2 inhibitor, dose-dependently prevented, ischemia-induced eicosanoid formation (area under the curve (AUC) of controls: 3.11 plus or minus 0.87; AUC of 20 mg/kg SC58236: 0.39 plus or minus 0.24), and caused significant reduction of damaged area (30.7 and 18.9% at SC58236 20 and 6.6 mg/kg), suggesting that selective inhibitors of CQX-2 are neuroprotective.
Author Masoero, Elisabetta
Scelsi, Roberto
Rozza, Annalinda
Govoni, Stefano
Viappiani, Serena
Favalli, Luigia
Sala, Angelo
Folco, Giancarlo
Buccellati, Carola
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  givenname: Carola
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  surname: Folco
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  organization: Institute of Pharmacological Sciences, University of Milan, Via Balzaretti 9, 20133 Milan, Italy
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Issue 2
Keywords Rats
Neuroprotection
Cerebral ischemia
Cyclooxygenase
Prostaglandin endoperoxide synthase
Animal model
Prostaglandin-endoperoxide synthase
Nervous system diseases
Rat
Enzyme
Rodentia
Enzyme inhibitor
Cardiovascular disease
Neuroprotective agent
Cerebral disorder
Vascular disease
Vertebrata
Mammalia
Ischemia
Central nervous system disease
Oxidoreductases
Cerebrovascular disease
Brain (vertebrata)
Language English
License CC BY 4.0
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Snippet Focal ischemia was induced in the fronto-parietal region of rat brain, by injection of Rose Bengal, followed by light activation. Focal ischemia was...
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SubjectTerms Animals
Biological and medical sciences
Brain Ischemia - drug therapy
Brain Ischemia - metabolism
Brain Ischemia - physiopathology
Cerebral Cortex - drug effects
Cerebral Cortex - pathology
Cerebral Cortex - physiopathology
Cerebral ischemia
Cyclooxygenase
Cyclooxygenase 2
Cyclooxygenase 2 Inhibitors
Cyclooxygenase Inhibitors - pharmacology
Disease Models, Animal
Dose-Response Relationship, Drug
Fluorescent Dyes - pharmacology
Isoenzymes - antagonists & inhibitors
Isoenzymes - metabolism
Male
Medical sciences
Microdialysis
Microscopy, Electron
Necrosis
Nerve Degeneration - etiology
Nerve Degeneration - physiopathology
Nerve Degeneration - prevention & control
Neurons - drug effects
Neurons - pathology
Neurons - ultrastructure
Neuropharmacology
Neuroprotection
Neuroprotective agent
Neuroprotective Agents - pharmacology
Pharmacology. Drug treatments
Prostaglandin D2 - antagonists & inhibitors
Prostaglandin D2 - metabolism
Prostaglandin endoperoxide synthase
Prostaglandin-Endoperoxide Synthases - metabolism
Pyrazoles
Rats
Rats, Wistar
Rose Bengal - pharmacology
Sulfonamides
Title The Cycloxygenase-2 inhibitor SC58236 is neuroprotective in an in vivo model of focal ischemia in the rat
URI https://dx.doi.org/10.1016/S0304-3940(01)01675-5
https://www.ncbi.nlm.nih.gov/pubmed/11311500
https://search.proquest.com/docview/18081346
https://search.proquest.com/docview/77072138
Volume 303
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