Subtle Alterations in Spatial Memory Induced by Amyloid Peptides Infusion in Rats
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2018
Autores
Macedo, Priscila Tavares
Aquino, Antônio Carlos Queiroz de
Meurer, Ywlliane da Silva Rodrigues [UNIFESP]
Brandão, Luiz Eduardo Mateus
Campelo, Clarissa Loureiro Chagas
Lima, Ramon Hypólito
Costa, Marcos R.
Ribeiro, Alessandra Mussi [UNIFESP]
Silva, Regina Helena [UNIFESP]
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The cause of Alzheimer’s disease (AD) remains uncertain. The accumulation of amyloid peptides (Aβ) is the main pathophysiological hallmark of the disease. Spatial deficit is an important initial sign of AD, while other types of memory impairments that appear in later stages. The Barnes maze allows the detection of subtle alterations in spatial search by the analysis of use of different strategies. Previous findings showed a general performance deficit in this task following long-term (35 days) infusion of Aβ, which corresponds to the moderate or severe impairments of the disease. In the present study, we evaluated the effects of a low-dose 15-day long treatment with Aβ peptides on spatial and non-spatial strategies of rats tested in the Barnes maze. Aβ peptides (0.5 μL/site/day; 30 pmoL solution of Aβ1–40:Aβ1–42 10:1) or saline were bilaterally infused into the CA1 (on the first treatment day) and intraventricularly (on the following 15 days) in 6-month-old Wistar male rats. Aβ infusion induced a deficit in the performance (increased latency and distance traveled to reach the target compared to saline group). In addition, a significant association between treatment and search strategy in the retrieval trial was found: Aβ group preferred the non-spatial search strategy, while saline group preferred the spatial search. In conclusion, the protocol of Aβ infusion used here induced a subtle cognitive deficit that was specific to spatial aspects. Indeed, animals under Aβ treatment still showed retrieval, but using non-spatial strategies. We suggest that this approach is potentially useful to the study of the initial memory deficits in early AD.
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Frontiers In Aging Neuroscience. Lausanne, v. 10, p. -, 2018.