Bioscience Biotechnology and Biochemistry · 2010 · 30 citations · 6 references
Life SciencesNeurosciencePharmacologyApoptosisMolecular NeuroscienceNeuropharmacologyCerebrovascular DiseaseHypoxic-ischemic Brain InjuryNeuronal Cell DeathNeuroprotectionNeuroprotective PharmacologyStrokeCerebral Hypoxic-ischemic InjuryCerebral Ischemia NeuroprotectionCerebral Oxygen Glucose DeprivationDeath-associated Protein Kinase SignalingIschemic Neuronal DeathNeural IschemiaNeuroprotective Drug DevelopmentStroke Neuroprotection
The purpose of this study was to determine whether the Laurus nobilis chloroform fraction (LNCF) protects against cerebral ischemia neuronal damage. Human neuroblastoma SH-SY5Y cells and brain slices from rats were subjected to oxygen and glucose deprivation (OGD), followed by reoxgenation with and without LNCF. The viabilities of SH-SY5Y cells and brain slices from the rats were 58.5±4.9% and 79.7±5.9% in the group subjected to OGD, and 80.4±0.4% and 97.2±1.9% at 4 µg/ml of LNCF, respectively. LNCF also significantly inhibited death-associated protein kinase (DAPK) dephosphorylation. Pretreatment with LNCF at 4 mg/kg significantly decreased infarct size by 79% of vehicle control in the middle cerebral artery occlusion (MCAO) in vivo model. LNCF is a neuroprotective drug candidate against cerebral ischemia neuronal damage.
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Reversible middle cerebral artery occlusion without craniectomy in rats.
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NMDA receptors are expressed in oligodendrocytes and activated in ischaemia
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