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Region-Specific and Age-Dependent Multitarget Effects of Acetylcholinesterase Inhibitor Tacrine on Comprehensive Neurotransmitter Systems

Authors :
Fridjonsdottir, Elva
Vallianatou, Theodosia
Mantas, Ioannis
Shariatgorji, Reza
Nilsson, Anna
Schembri, Luke S
Odell, Luke R.
Svenningsson, Per
Andrén, Per E.
Fridjonsdottir, Elva
Vallianatou, Theodosia
Mantas, Ioannis
Shariatgorji, Reza
Nilsson, Anna
Schembri, Luke S
Odell, Luke R.
Svenningsson, Per
Andrén, Per E.
Publication Year :
2022

Abstract

Regional brain distribution and metabolism of neurotransmitters and their response to drug treatment are fundamentally important for understanding the central effects of neuroactive substances. We used matrix-assisted laser desorption/ionization mass spectrometry imaging in combination with multivariate analysis to visualize in anatomical detail metabolic effects of aging and tacrine-mediated acetylcholinesterase inhibition on comprehensive neurotransmitter systems in multiple mouse brain regions of 12-week-old and 14-month-old mice. We detected age-related increases in 3,4-dihydroxyphenylacetaldehyde and histamine, indicating oxidative stress and aging deficits in astrocytes. Tacrine had a significant impact on the metabolism of neurotransmitters in both age groups; predominantly, there was an increased norepinephrine turnover throughout the brain and decreased 3-methoxy tyramine, a marker for dopamine release, in the striatum. The striatal levels of histamine were only elevated after tacrine administration in the older animals. Our results demonstrated that tacrine is a multitarget and region-specific neuroactive agent, inducing age-specific responses. Although well-studied, the complete mechanisms of the action of tacrine are not fully understood, and the current findings reveal features that may help explain its treatment-related effectiveness and central side effects.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1312722191
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1021.acschembio.1c00803