Acetylcholinesterase induces neuronal cell loss, astrocyte hypertrophy and behavioral deficits in mammalian hippocampus

Chacón MA; Reyes, AE; Inestrosa, NC

Abstract

Previous studies have demonstrated that acetylcholinesterase (AChE) promotes the assembly of amyloid-?-peptides into neurotoxic amyloid fibrils and is toxic for chick retina neuronal cultures and neuroblastoma cells. Moreover, AChE is present in senile plaques in Alzheimer's disease (AD) brains. Here we have studied the effect of AChE on astrocytes and hippocampal neurons in vivo. Morphological as well as behavioral disturbances were analyzed after intrahippocampal injection of AChE. Rats were trained in the Morris water maze and assayed for behavioral parameters. Neuronal cell loss was found in the upper leaf of the dentate gyrus in rats injected with AChE in comparison with control animals. Glial fibrillary acidic protein immunoreactivity showed astrocytic hypertrophy and the magnitude of the response was associated with neuronal cell loss. Behavioral results show that injection of AChE produces cognitive impairment demonstrated by an altered water maze performance including (i) a higher escape latency score, (ii) a decreased spatial acuity and (iii) a shorter time of swimming in the platform quadrant. These findings indicate that a local increment in neuronal AChE concentration at the mammalian hippocampus, such as those present in amyloid deposits, may play a role in triggering neuropathological and behavioral changes such as those observed in AD brains.

Más información

Título según WOS: Acetylcholinesterase induces neuronal cell loss, astrocyte hypertrophy and behavioral deficits in mammalian hippocampus
Título según SCOPUS: Acetylcholinesterase induces neuronal cell loss, astrocyte hypertrophy and behavioral deficits in mammalian hippocampus
Título de la Revista: JOURNAL OF NEUROCHEMISTRY
Volumen: 87
Número: 1
Editorial: Wiley
Fecha de publicación: 2003
Página de inicio: 195
Página final: 204
Idioma: English
URL: http://doi.wiley.com/10.1046/j.1471-4159.2003.01985.x
DOI:

10.1046/j.1471-4159.2003.01985.x

Notas: ISI, SCOPUS