Chronic (-)-deprenyl administration attenuates dendritic developmental impairment induced by early social isolation in the rat

Pascual, R.; Zamora-Leon, SP

Abstract

It has been demonstrated that postweaning social isolation alters dendritic development in the medial prefrontal cortex (mPFC) of the rat. In addition, (-)-deprenyl, a monoamine oxidase B (MAO-B) inhibitor, promotes dendritic growth in prefrontocortical pyramidal cells. This study examined whether prefrontocortical dendritic developmental impairment induced by postweaning social isolation is attenuated by chronic (-)-deprenyl administration. Weanling Sprague-Dawley male rats were randomly reared in social and isolated environments between postnatal days 21 and 51 (P21-P51). At P52, half of the animals were behaviorally evaluated in the open-field test and sacrificed for histological analysis. The remaining isolated rats were subdivided into saline- and daily (-)-deprenyl-treated animals for 30 additional days (P52-P82). Socially-reared rats remained undisturbed except for daily saline administration. At P82, all animals were behaviorally evaluated and sacrificed for histological analysis. Dendritic quantification of the Golgi-Cox-Sholl- stained neurons indicated that chronic (-)-deprenyl administration partially compensated the dendritic growth impairment induced by social isolation. In addition, both isolated-saline- and (-)-deprenyl-treated rats showed a sustained locomotor hyperactivity in the open-field test. Copyright © 2006 S. Karger AG, Basel.

Más información

Título según WOS: Chronic (-)-deprenyl administration attenuates dendritic developmental impairment induced by early social isolation in the rat
Título según SCOPUS: Chronic (-)-deprenyl administration attenuates dendritic developmental impairment induced by early social isolation in the rat
Título de la Revista: DEVELOPMENTAL NEUROSCIENCE
Volumen: 29
Número: 3
Editorial: Karger
Fecha de publicación: 2007
Página de inicio: 261
Página final: 267
Idioma: English
URL: http://www.karger.com/doi/10.1159/000096413
DOI:

10.1159/000096413

Notas: ISI, SCOPUS