Abstract

The neurotransmitter of the cholinergic system, acetylcholine plays a major role in the brain’s cognitive function and is involved in neurodegenerative disorders. Here, we present age-related alterations of acetylcholine levels after administration of the acetylcholinesterase inhibitor drug tacrine in normal mice. Using a quantitative, robust and molecular-specific mass spectrometry imaging method we found that tacrine administration significantly raised acetylcholine levels in most areas of sectioned mice brains, inter alia the striatum, hippocampus and cortical areas. However, acetylcholine levels in retrosplenial cortex were significantly lower in 14-month-old than in 12-week-old animals following its administration, indicating that normal aging affects the cholinergic system’s responsivity. This small brain region is interconnected with an array of brain networks and is involved in numerous cognitive tasks. Simultaneous visualization of distributions of tacrine and its hydroxylated metabolites in the brain revealed a significant decrease in levels of the metabolites in the 14-month-old mice. The results highlight strengths of the imaging technique to simultaneously investigate multiple molecular species and the drug–target effects in specific regions of the brain. The proposed approach has high potential in studies of neuropathological conditions and responses to neuroactive treatments.

Highlights

  • Acetylcholine (ACh), the neurotransmitter of the cholinergic system, plays crucial roles in both the central (CNS) and autonomous nervous system

  • Loss of cholinergic neurons in these brain structures is associated with development of pathophysiological neurodegenerative states such as dementias, including Alzheimer’s disease (AD) [3]

  • The effect of aging on the cholinergic system has been studied using several approaches, mainly focusing on activities of enzymes involved in ACh synthesis and degradation [4]

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Summary

Introduction

Acetylcholine (ACh), the neurotransmitter of the cholinergic system, plays crucial roles in both the central (CNS) and autonomous nervous system. Inter alia, it is essential for healthy brain cognitive function, and one of the neurotransmitters with the greatest effects on memory [1]. Loss of cholinergic neurons in these brain structures is associated with development of pathophysiological neurodegenerative states such as dementias, including Alzheimer’s disease (AD) [3]. This cholinergic decline is associated with aging and various other pathophysiological, genetic and environmental risk factors [4]. Conflicting results have been reported [5], indicating that senescence-induced neurochemical alterations are complex

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