RESUMEN
Studies have shown that schizophrenic patients seem to have nutritional deficiencies. Ascorbic acid (AA) has an important antioxidant effect and neuromodulatory properties. The aim of this study was to evaluate the effects of AA on locomotor activity and the acetylcholinesterase activity (AChE) in an animal model of schizophrenia (SZ). Rats were supplemented with AA (0.1, 1, or 10 mg/kg), or water for 14 days (gavage). Between the 9th and 15th days, the animals received Ketamine (Ket) (25 mg/kg) or saline (i.p). After the last administration (30 min) rats were subjected to the behavioral test. Brain structures were dissected for biochemical analysis. There was a significant increase in the locomotor activity in Ket treated. AA prevented the hyperlocomotion induced by ket. Ket also showed an increase of AChE activity within the prefrontal cortex and striatum prevented by AA. Our data indicates an effect for AA in preventing alterations induced by Ket in an animal model of SZ, suggesting that it may be an adjuvant approach for the development of new therapeutic strategies within this psychiatric disorder.
Asunto(s)
Acetilcolinesterasa/análisis , Acetilcolinesterasa/efectos de los fármacos , Antioxidantes/farmacología , Ácido Ascórbico/farmacología , Locomoción/efectos de los fármacos , Esquizofrenia/enzimología , Esquizofrenia/prevención & control , Acetilcolinesterasa/fisiología , Animales , Cuerpo Estriado/efectos de los fármacos , Cuerpo Estriado/enzimología , Suplementos Dietéticos , Modelos Animales de Enfermedad , Antagonistas de Aminoácidos Excitadores , Hipocampo/efectos de los fármacos , Hipocampo/enzimología , Ketamina , Locomoción/fisiología , Masculino , Corteza Prefrontal/efectos de los fármacos , Corteza Prefrontal/enzimología , Ratas Wistar , Valores de Referencia , Reproducibilidad de los Resultados , Esquizofrenia/inducido químicamente , Esquizofrenia/fisiopatologíaRESUMEN
ABSTRACT Studies have shown that schizophrenic patients seem to have nutritional deficiencies. Ascorbic acid (AA) has an important antioxidant effect and neuromodulatory properties. The aim of this study was to evaluate the effects of AA on locomotor activity and the acetylcholinesterase activity (AChE) in an animal model of schizophrenia (SZ). Rats were supplemented with AA (0.1, 1, or 10 mg/kg), or water for 14 days (gavage). Between the 9th and 15th days, the animals received Ketamine (Ket) (25 mg/kg) or saline (i.p). After the last administration (30 min) rats were subjected to the behavioral test. Brain structures were dissected for biochemical analysis. There was a significant increase in the locomotor activity in Ket treated. AA prevented the hyperlocomotion induced by ket. Ket also showed an increase of AChE activity within the prefrontal cortex and striatum prevented by AA. Our data indicates an effect for AA in preventing alterations induced by Ket in an animal model of SZ, suggesting that it may be an adjuvant approach for the development of new therapeutic strategies within this psychiatric disorder.