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Acta Neuropsychiatr ; 26(3): 146-54, 2014 Jun.
Article in English | MEDLINE | ID: mdl-25142190

ABSTRACT

OBJECTIVES: Mazindol is a sympathomimetic amine, widely used as an anorectic agent in the treatment of obesity. This drug causes psychostimulant effects because of its pharmacological profile similar to amphetamine, acting like a monoamine reuptake inhibitor. However, the mechanisms underlying the action of mazindol are still not clearly understood. METHODS: Swiss mice received a single acute administration of mazindol (0.25, 1.25 and 2.5 mg/kg, ip) or saline. After 2 h, the animals were killed by decapitation; the brain was removed and used for the evaluation of activities of mitochondrial respiratory chain complexes, Krebs cycle enzymes and creatine kinase. RESULTS: Acute administration of mazindol decreased complex I activity only in the hippocampus. Complex IV activity was increased in the cerebellum (2.5 mg/kg) and cerebral cortex (0.25 mg/kg). Citrate synthase activity was increased in the cerebellum (1.25 mg/kg) and cerebral cortex (1.25 mg/kg), and creatine kinase activity was increased in the cerebellum (1.25 mg/kg). CONCLUSION: We suggest that the inhibition of complex I in the hippocampus only and activation of complex IV, citrate synthase and creatine kinase occurs because of a stimulus effect of mazindol in the central nervous system, which causes a direct impairment on energy metabolism.


Subject(s)
Brain/drug effects , Brain/metabolism , Central Nervous System Stimulants/pharmacology , Energy Metabolism/drug effects , Mazindol/pharmacology , Animals , Central Nervous System Stimulants/administration & dosage , Central Nervous System Stimulants/therapeutic use , Male , Mazindol/administration & dosage , Mazindol/therapeutic use , Mice , Obesity/drug therapy , Obesity/metabolism
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