ABSTRACT
Intermittent fasting diet (IF) as a restrictive regimen prevents neural degeneration and stimulates overexpression of various neurotropic factors in the hippocampus of animal models. This study evaluates the potential effect of the IF in the prevention of learning and memory dysfunction and improving the alterations in the number and volume of neurons in an ethidium bromide (EB) induced mouse model of demyelination.Mice were randomly assigned into N group (Normal Diet and normal saline injection), F group (IF and normal saline injection), EBN group (Normal Diet and EB injection), EBF group (IF and EB injection). The hidden platform test was carried out based on path length, escape latency and swim speeds of mice. Stereological studies were determined by the Cavalieri and the Optical Dissector technique. Maintenance of mice on the IF results in significantly decreased the body weight and biochemical parameters, increased total number of neurons and volume of the hippocampus, and improved learning and memory parameters of adult male mice. However, IF in EBF group did not show as excellently as F group. The EBF group displayed significantly spatial memory improvement than that in EBN group. There were no statistically significant differences between EBF and EBN groups in stereological and learning parameters, though the EBF group displayed faster escape latencies, and swam faster and shorter path lengths than the EBN group in these parameters. Therefore as a conclusion, The IF fairly improved some adverse effects of EB in experimental demyelination models.
La dieta de ayuno intermitente (AI) como régimen restrictivo, previene la degeneración neural y la estimación de la presencia de diversos factores neurotrópicos en el hipocampo de modelos animales. Este estudio evalúa el efecto potencial de la AI en la prevención del aprendizaje y la disfunción de la memoria y mejora las alteraciones en el número y el volumen de las neuronas en un modelo de desmielinización, en ratón, inducido con bromuro de etidio (BE). Los ratones se asignaron al azar en el grupo N (dieta normal e inyección salina normal), Grupo A (AI e inyección salina normal), Grupo BEN (dieta normal e inyección BE), Grupo EBF (inyección AI y BE). La prueba de la plataforma oculta se llevó a cabo en función de la longitud del trayecto, la latencia de escape y la velocidad de nado de los ratones. Los estudios estereológicos fueron determinados por la técnica de Cavalieri y la técnica del disector óptico. En el grupo AI disminuyeron significativamente el peso corporal de los ratones, los parámetros bioquímicos, el número total de neuronas y el volumen del hipocampo, y los parámetros de aprendizaje y la memoria de los ratones machos adultos. Sin embargo, el grupo AI en BEF no se mostró tan bien como el grupo A. El grupo EBF mostró una mejora en la memoria espacial significativamente mayor que la del grupo BEN. No hubo diferencias estadísticamente significativas entre los grupos A, BE y BEN en los parámetros estereológicos y de aprendizaje, aunque el grupo EBF mostró latencias de escape más rápidas, y nado en las rutas más rápidas y más cortas que el grupo BEN en estos parámetros. Por lo tanto, como conclusión, el grupo AI mejoró bastante algunos efectos adversos de la BE en los modelos de desmielinización experimental.
Subject(s)
Animals , Male , Mice , Fasting , Demyelinating Diseases/chemically induced , Hippocampus/pathology , Body Weight , Disease Models, Animal , Ethidium/toxicity , Learning , Mice, Inbred BALB CABSTRACT
A common pathology in Traumatic brain injury (TBI) is brain edema that develops within hours of impact. It causes increased intracranial pressure (ICP), and nerve damage. It was shown that Walnut kernel (WK) has a large amount of phenolic compounds with beneficial effects on human health due to antioxidant and anti- inflammatory properties. The present study was designed to investigate the effect of WK feeding on brain edema, neurological score and neuronal degeneration in male rat after traumatic brain injury. The diffuse TBI was induced in adult male rats using Marmarou’s method. Sixty days prior to the injury, WK was added to ordinary food (6% percent of daily food). Experimental groups are included sham (no TBI and no WK), control (TBI and no WK) and treatment (TBI and WK). Brain edema and neuronal injury were measured 72 h after TBI. Veterinary Coma Scale (VCS) and ICP were assessed at -1, 4, 24, 48 and 72 h after TBI. Brain water content and ICP in treatment group decreased as compared to the control. Besides, VCS at 24, 48 and 72 h after TBI showed a significant increase in treatment group in comparison with control. Based on our data, WK pre-treatment may reduce pathological parameters after TBI in male rats.