Interactions between physical exercise, associative memory, and genetic risk for Alzheimer’s disease

Author:

Igloi Kinga12ORCID,Marin Bosch Blanca1,Kuenzi Noémie1,Thomas Aurélien3456,Lauer Estelle56,Bringard Aurélien7,Schwartz Sophie128

Affiliation:

1. Department of Fundamental Neurosciences, University of Geneva , CH-1211 Geneva , Switzerland

2. Swiss Center for Affective Sciences, University of Geneva , CH-1211 Geneva , Switzerland

3. Faculty Unit of Toxicology , CURML, Faculty of Biology and Medicine, , CH-1015 Lausanne , Switzerland

4. University of Lausanne , CURML, Faculty of Biology and Medicine, , CH-1015 Lausanne , Switzerland

5. Unit of Forensic Toxicology and Chemistry , CURML, , Lausanne, CH-1011 Geneva , Switzerland

6. Lausanne and Geneva University Hospitals , CURML, , Lausanne, CH-1011 Geneva , Switzerland

7. Department of Pneumology, Geneva University Hospitals , CH-1011 Geneva , Switzerland

8. Geneva Neuroscience Center, University of Geneva , CH-1211 Geneva , Switzerland

Abstract

Abstract The ε4 allele of the APOE gene heightens the risk of late onset Alzheimer’s disease. ε4 carriers, may exhibit cognitive and neural changes early on. Given the known memory-enhancing effects of physical exercise, particularly through hippocampal plasticity via endocannabinoid signaling, here we aimed to test whether a single session of physical exercise may benefit memory and underlying neurophysiological processes in young ε3 carriers (ε3/ε4 heterozygotes, risk group) compared with a matched control group (homozygotes for ε3). Participants underwent fMRI while learning picture sequences, followed by cycling or rest before a memory test. Blood samples measured endocannabinoid levels. At the behavioral level, the risk group exhibited poorer associative memory performance, regardless of the exercising condition. At the brain level, the risk group showed increased medial temporal lobe activity during memory retrieval irrespective of exercise (suggesting neural compensatory effects even at baseline), whereas, in the control group, such increase was only detectable after physical exercise. Critically, an exercise-related endocannabinoid increase correlated with task-related hippocampal activation in the control group only. In conclusion, healthy young individuals carrying the ε4 allele may present suboptimal associative memory performance (when compared with homozygote ε3 carriers), together with reduced plasticity (and functional over-compensation) within medial temporal structures.

Funder

Swiss National Science Foundation

Publisher

Oxford University Press (OUP)

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