Neuroprotective effect of fluoxetine in an experimental model of brain ischemia in mice
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Keywords

Fluoxetina
Isquemia cerebral
Ratones
Agentes neuroprotectores
Regeneración nerviosa
Plasticidad neuronal
Trastornos psicomotores Fluoxetine
Brain ischemia
Mice
Neuroprotective agents
Nerve regeneration
Neuronal plasticity
Psychomotor disorders

How to Cite

Londoño, A. C., & Arango Dávila, C. A. (2011). Neuroprotective effect of fluoxetine in an experimental model of brain ischemia in mice. Revista Médica Sanitas, 14(4), 30-38. Retrieved from //revistas.unisanitas.edu.co/index.php/rms/article/view/350

Abstract

Introduction: fluoxetine is a drug of wide use in the treatment of mood disorders. In these conditions have been observed direct effects on neuronal plasticity and neuroregenerative properties. Objective: to evaluate the impact of fluoxetine over neurological impairment and ischemic volume in a model of brain ischemia. Design: we use 28 mice distributed into four experimental groups: fluoxetine and placebo with and without ischemic injury. Fluoxetine was administered by intraperitoneal injection at dose 20 mg/kg/day once daily for 21 days before ischemic surgery. The focal cerebral ischemia technique consist in enter through the internal carotid artery a monofilament nylon coated with poly-l-lysine until occlude middle cerebral artery, 30 minutes later the nylon is removed from the arterial, allowing vascular reperfusion. 24 hours after ischemia, the animals were behavioral neurological assessment using the modified Bederson scale and open-field behavioral test. After this, ischemic volume was determined using the method 2,3,5-Triphenyltetrazolium chloride. Results: mice treated with fluoxetine who underwent the procedure cerebral ischemia-reperfusion had a lower neurological deficit (p = 0.0001) and lower percentage of injury (p = 0.003), which was significantly correlated with improved of psychomotor disorders. Conclusions: fluoxetine seems to have a neuroprotective effect on cerebral isquemic in mouses. Our findings encourage us to continue studying its effect in future preclinical and clinical trials in patients with stroke and brain injury.

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