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Influence of Lifestyle on Brain Sensitivity to Circulating Insulin-like Growth Factor 1

  • Jonathan Zegarra-Valdivia(corresponding author)
    ,
  • M. Zahid Khan
    ,
  • Aurora Putzolu
    ,
  • Raffaela Cipriani
    ,
  • Jaime Pignatelli
    ,
  • Ignacio Torres Aleman(corresponding author)
*Corresponding author for this work
  • ,
  • Psychology Department
    ,
  • Achucarro Basque Center for Neuroscience
    ,
  • CIBERNED
    ,
  • Cajal Institute (CSIC)
    ,
  • Basque Foundation for Science
Research Output:
Contribution to journal
Article
Research
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Research
Peer-review

Original language

English

Article number

10008

Journal (Volume, Issue Number)

International Journal of Molecular Sciences (Volume 26, Issue 20)

Publication milestones

  • Published - 10/2025

Publication status

Published - 10/2025

ISSN

1661-6596

Publication IDs

  • Scopus: 105020306138
  • PubMed: 41155299

Abstract

Lifestyle factors, including social relationships and diet, influence mood homeostasis, a mechanism often dysregulated in high-incidence mental illnesses like depression and Alzheimer’s dementia (AD). Given that insulin-like growth factor 1 (IGF-1) modulates mood and its blood levels are altered in both AD and affective disorders, we investigated whether IGF-1 activity in the brain was affected in mice subjected to social isolation or a high-fat diet (HFD). We found that both lifestyle conditions increased anxiety and depression-like behavior in C57BL/6 mice of both sexes, as determined by the elevated zero maze/open field tests and the forced swim test, respectively. These lifestyle conditions were associated with loss of neuronal responses to systemic IGF-1. Enhanced neuronal activity in the prefrontal cortex—measured via Ca++ fiber photometry following intraperitoneal IGF-1 administration—was absent in both socially isolated and HFD-fed mice. However, only the HFD-fed group exhibited elevated serum IGF-1 levels. These findings suggest that loss of brain IGF-1 input may contribute to the observed mood disturbances, providing potential new targets to explore the heightened risk of depression and AD associated with loneliness and unhealthy diets in humans. Importantly, because reduced IGF-1 activity in the brain is not consistently reflected in serum levels, serum measurements are an unreliable indicator of brain IGF-1 activity.

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