Calpain inhibitor A-558693 in experimental focal cerebral ischemia in rats
| Autor: | Gerhard F. Hamann, Nora Thomassen, Dorothe Burggraf, Wolfgang Lubisch, Helge K. Martens, Achim Möller, Martin Liebetrau, Dusica Gabrijelcic-Geiger |
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| Rok vydání: | 2005 |
| Předmět: |
Brain Infarction
Male Proteases Pathology medicine.medical_specialty Blotting Western Ischemia Cell Count Brain Ischemia medicine.artery Basal ganglia Medicine Animals Enzyme Inhibitors Rats Wistar biology business.industry Calpain Infarction Middle Cerebral Artery General Medicine medicine.disease Amides Immunohistochemistry Rats Blot Disease Models Animal Neurology Gene Expression Regulation Anesthesia Reperfusion Injury Middle cerebral artery biology.protein Neurology (clinical) business Intracellular |
| Zdroj: | Neurological research. 27(5) |
| ISSN: | 0161-6412 |
| Popis: | Calpains are intracellular proteases, which are activated in various cerebral injuries. We studied the expression of mu-calpain in a model of focal cerebral ischemia/reperfusion and the efficacy of the calpain inhibitor A-558693.A transient occlusion of the middle cerebral artery was produced in male Wistar rats by using the suture model with 3 hours of ischemia and 24 hours of reperfusion. Six animals were given the calpain inhibitor and six animals were treated with placebo. The infarct size was determined by the loss of the calpain substrate microtubule-associated protein-2 (MAP-2) immunohistochemistry using volumetry in serial slices of the brains. Furthermore mu-calpain positive-stained cells were detected by immunohistochemistry and western blotting.In placebo-treated animals the mu-calpain expression was significantly increased in the ischemic hemisphere compared with the contralateral non-ischemic hemisphere (88.6 versus 10.5% in the basal ganglia, 60.7 versus 10.7% in the cortex, p0.001, respectively) with a subsequent loss its substrate MAP-2. However, the use of the calpain inhibitor A-558693 did not significantly change the mu-calpain expression, nor significantly reduce the infarct volume.The present data indicate that mu-calpain proteolysis plays an important role in the chain of events following cerebral ischemia. However, the calpain inhibitor A-558693 failed to prevent these changes. |
| Databáze: | OpenAIRE |
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