4.6 Article

Activation of cholinergic system partially rescues olfactory dysfunction-induced learning and memory deficit in mice

Journal

BEHAVIOURAL BRAIN RESEARCH
Volume 408, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.bbr.2021.113283

Keywords

Choline acetyltransferase; Hippocampus; Memory; Olfactory function; Zinc sulfate

Funding

  1. [19K23808]

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This study found that intranasal zinc sulfate-treated mice exhibited olfactory dysfunction and impaired short-term and long-term learning and memory. Olfaction dysfunction was significantly correlated with short-term memory, and treatment with zinc sulfate altered the choline acetyltransferase levels in the olfactory bulb.
Deficits in olfaction are associated with neurodegenerative disorders such as Alzheimer?s disease. A recent study reported that intranasal zinc sulfate (ZnSO4)-treated mice show olfaction and memory deficits. However, it remains unknown whether olfaction deficit-induced learning and memory impairment is associated with the cholinergic system in the brain. In this study, we evaluated olfactory function by the buried food find test, and learning and memory function by the Y-maze and passive avoidance tests in ZnSO4-treated mice. The expression of choline acetyltransferase (ChAT) protein in the olfactory bulb (OB), prefrontal cortex, hippocampus, and amygdala was assessed by western blotting. Moreover, we observed the effect of the acetylcholinesterase inhibitor physostigmine on ZnSO4-induced learning and memory deficits. We found that intranasal ZnSO4-treated mice exhibited olfactory dysfunction, while this change was recovered on day 14 after treatment. Both short-term and long-term learning and memory were impaired on days 4 and 7 after treatment with ZnSO4, whereas the former, but not the latter, was recovered on day 14 after treatment. A significant correlation was observed between olfactory function and short-term memory, but not long-term memory. Treatment with ZnSO4 decreased the ChAT level in the OB on day 4, and increased and decreased the ChAT levels in the OB and hippocampus on day 7, respectively. Physostigmine improved the ZnSO4-induced deficit in short-term, but not long-term, memory. Taken together, the present results suggest that short-term memory may be closely associated with olfactory function via the cholinergic system.

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