Abstract

The aging brain is characterized by altered dopamine signaling. The amino acid tyrosine, a catecholamine precursor, is known to improve cognitive performance in young adults, especially during high environmental demands. Tyrosine administration might also affect catecholamine transmission in the aging brain, thereby improving cognitive functioning. In healthy older adults, we previously demonstrated impairments in two forms of response inhibition: reactive inhibition (outright stopping) and proactive inhibition (anticipatory response slowing) under high information load. However, no study has directly compared the effects of a catecholamine precursor on reactive and load-dependent proactive inhibition. In this study we explored the effects of tyrosine on reactive and proactive response inhibition and signal in dopaminergically innervated fronto-striatal regions. Depending on age, tyrosine might lead to beneficial or detrimental neurocognitive effects. We aimed to address these hypotheses in 24 healthy older adults (aged 61-72 years) using fMRI in a double blind, counterbalanced, placebo-controlled, within-subject design. Across the group, tyrosine did not alter reactive or proactive inhibition behaviorally, but did increase fronto-parietal proactive inhibition-related activation. When taking age into account, tyrosine affected proactive inhibition both behaviorally and neurally. Specifically, increasing age was associated with a greater detrimental effect of tyrosine compared with placebo on proactive slowing. Moreover, with increasing age, tyrosine decreased fronto-striatal and parietal proactive signal, which correlated positively with tyrosine’s effects on proactive slowing. To conclude, tyrosine negatively affected proactive response slowing and associated fronto-striatal activation in an age-dependent manner, highlighting the importance of catecholamines, perhaps particularly dopamine, for proactive response inhibition in older adults.

Highlights

  • The aging brain is characterized by alterations in dopamine functioning (Kaasinen and Rinne, 2002; Braskie et al, 2008)

  • Age negatively modulated the effect of tyrosine on proactive response slowing: increasing age was associated with a greater detrimental effect of tyrosine on proactive slowing compared with placebo

  • The current study investigated the neuro-cognitive effects of acute tyrosine administration, a dopamine precursor, on reactive and proactive response inhibition in a healthy older sample

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Summary

Introduction

The aging brain is characterized by alterations in dopamine functioning (Kaasinen and Rinne, 2002; Braskie et al, 2008). Age-related decreases in dopamine receptor and transporter binding have been linked to impairments in cognitive functions such as attention, episodic and working memory (Bäckman et al, 2006) and age-related increases in dopamine synthesis capacity have been related to decreased neural reward processing (Dreher et al, 2008). Administration of a D1 receptor agonist improved working memory performance (Cai and Arnsten, 1997). Enhancing dopamine levels in humans with the drug L-Dopa (the direct dopamine precursor) improved age-related impairments in episodic memory performance and reinforcement learning (Chowdhury et al, 2012, 2013). Tyrosine administration improved cognitive control functions such as response inhibition, task switching, and working memory, especially in demanding circumstances (for review, see Deijen, 2005; Jongkees et al, 2015).

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