Τίτλος:
Expression of S100B protein in ischemia/ reperfusion-induced brain injury after cyclosporine therapy: A biochemical serum marker with prognostic value?
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Background: Accumulating evidence has indicated that S100B protein may be involved in the pathophysiology of ischemia-reperfusion brain injury. Cyclosporine has been shown to have neuroprotective functions. This study investigated the effect of cyclosporine on S100B serum levels and the severity of brain tissue damage in a rat model of cerebral ischemia-reperfusion (I/R). Material/Methods: Twelve-week-old Wistar male rats were randomly divided into Control I/R and Cyclosporine I/R groups (n=10 each). Cyclosporine was given orally by gavage for 5 days prior to cerebral I/R, at a total volume of 15 mg/kg/day. The Control group received an equal volume of saline. Body weight was measured and all animals were subjected to 60-min focal ischemia by filament occlusion of the middle cerebral artery. ELISA was used to assess the concentrations of serum S100B and development of brain infarct size and neurological outcomes were determined at 2 and 24 h after occlusion withdrawal. Results: Cyclosporine improved the neurological deficit score and decreased the cerebral infarct size and body weight. S100B serum levels were significantly elevated in Cyclosporine-treated rats compared with untreated Control rats during the reperfusion phase. Total infarct size was positively associated with S100B serum levels in the Control I/R group, but no significant correlation was observed in the Cyclosporine I/R group. Conclusions: Cyclosporine seems to affect both ischemia-reperfusion brain tissue damage and S100B protein serum levels. S100B serum level appears to be a state marker for the severity of the cerebral ischemia-reperfusion, rather than a trait marker for Cyclosporine responsiveness. © Med Sci Monit.
Συγγραφείς:
Dimopoulos, C.
Damaskos, C.
Papadakis, M.
Garmpis, N.
Kontzoglou, K.
Perrea, D.
Moraitis, S.
Daskalopoulou, A.
Papaspirou, I.
Georgopoulos, S.
Nikiteas, N.
Περιοδικό:
Medical science monitor: international medical journal of experimental and clinical research
Εκδότης:
International Scientific Information, Inc.
Λέξεις-κλειδιά:
biological marker; cyclosporine; protein S100B; biological marker; cyclosporine; neuroprotective agent; protein S100B; S100b protein, rat, angiogenesis; animal model; animal tissue; Article; biochemistry; blood sampling; body weight; brain infarction; brain infarction size; brain injury; brain ischemia; carotid artery obstruction; cerebrovascular accident; controlled study; digital subtraction angiography; drug delivery system; enzyme linked immunosorbent assay; histopathology; internal carotid artery; ischemia reperfusion induced brain injury; ischemia reperfusion induced brain injury; male; middle cerebral artery; nerve cell degeneration; neuroprotection; nonhuman; pathophysiology; prognosis; rat; reperfusion injury; tissue injury; animal; blood; brain; brain injury; brain ischemia; metabolism; physiology; Wistar rat, Animals; Biomarkers; Brain; Brain Injuries; Brain Ischemia; Cerebral Infarction; Cyclosporine; Male; Neuroprotective Agents; Prognosis; Rats; Rats, Wistar; Reperfusion Injury; S100 Calcium Binding Protein beta Subunit
