Levodopa suppresses grid-like activity and impairs spatial learning in novel environments in healthy young adults

Author:

Gönner Lorenz123,Baeuchl Christian123,Glöckner Franka12,Riedel Philipp3,Smolka Michael N3,Li Shu-Chen124

Affiliation:

1. Faculty of Psychology , Chair of Lifespan Developmental Neuroscience, , 01062 Dresden , Germany

2. TU Dresden , Chair of Lifespan Developmental Neuroscience, , 01062 Dresden , Germany

3. Department of Psychiatry, TU Dresden , 01307 Dresden , Germany

4. Centre for Tactile Internet With Human-in-the-Loop, TU Dresden , 01062 Dresden , Germany

Abstract

Abstract Accumulated evidence from animal studies suggests a role for the neuromodulator dopamine in memory processes, particularly under conditions of novelty or reward. Our understanding of how dopaminergic modulation impacts spatial representations and spatial memory in humans remains limited. Recent evidence suggests age-specific regulation effects of dopamine pharmacology on activity in the medial temporal lobe, a key region for spatial memory. To which degree this modulation affects spatially patterned medial temporal representations remains unclear. We reanalyzed recent data from a pharmacological dopamine challenge during functional brain imaging combined with a virtual object-location memory paradigm to assess the effect of Levodopa, a dopamine precursor, on grid-like activity in the entorhinal cortex. We found that Levodopa impaired grid cell-like representations in a sample of young adults (n = 55, age = 26–35 years) in a novel environment, accompanied by reduced spatial memory performance. We observed no such impairment when Levodopa was delivered to participants who had prior experience with the task. These results are consistent with a role of dopamine in modulating the encoding of novel spatial experiences. Our results suggest that dopamine signaling may play a larger role in shaping ongoing spatial representations than previously thought.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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