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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Stereological investigation of the CA1 pyramidal cell layer in untreated and lithium-treated 3xTg-AD and wild-type mice

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Author(s):
Schaeffer, Evelin L. ; Catanozi, Sergio ; West, Mark J. ; Gattaz, Wagner F.
Total Authors: 4
Document type: Journal article
Source: ANNALS OF ANATOMY-ANATOMISCHER ANZEIGER; v. 209, p. 51-60, 2017.
Web of Science Citations: 6
Abstract

Pyramidal neuron loss in the hippocampal CM region is a very early hallmark of Alzheimer disease (AD). Lithium might be a therapeutic strategy for AD due to its neuroprotective and neurotrophic properties. This study used modern stereological techniques to investigate possible CM pyramidal neuron loss in 11-month-old triple transgenic AD (3xTg-AD) mice, and also the effects of therapeutic and subtherapeutic lithium doses on the number and density of CAl pyramidal neurons and volume of CAl pyramidal layer in 3xTg-AD and wild-type mice treated from 3 toil months of age. 3xTg-AD mice displayed CM pyramidal layer atrophy that is likely due to reduced neuronal volume because of the absence of neuronal loss. Both lithium treatments of 3xTg-AD mice, which already expressed AD-like pathology, had no effect on CM atrophy. However, lithium treatment of wild-type mice, at low (subtherapeutic) doses, induced a significant increase in total CM pyramidal neuron number that led to a significant increase in total CAl pyramidal layer volume. The lithium-induced increase in CM neuron number is highly consistent with previous evidence that adult neurogenesis can be exogenously induced in the CM pyramidal layer with impact on total CAl neuron number, thus raising the possibility of the chronic use of low-dose lithium as a strategy to help compensate for neuronal loss in CM and perhaps other typically non-neurogenic brain regions in various neurological diseases. With regard to AD, low-dose lithium intervention must be initiated as early as possible in the course of neuropathology for beneficial effects to occur. (C) 2016 Elsevier GmbH. All rights reserved. (AU)

FAPESP's process: 09/52825-8 - Neurobiology of Alzheimer's disease: risk markers, prognosis and therapeutic response
Grantee:Wagner Farid Gattaz
Support Opportunities: Research Projects - Thematic Grants