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Serum Insulin-like growth factor i deficiency associates to Alzheimer's disease Co-morbidities

  • ,
  • Andrea Santi
    ,
  • Maria Estrella Fernández De Sevilla
    ,
  • Angel Nuñez
    ,
  • Ignacio Torres Aleman(corresponding author)
*Corresponding author for this work
  • ,
  • Facultad de Medicina de la Universidad Nacional de San Agustín
    ,
  • Instituto de Salud Carlos III
    ,
  • Cajal Institute (CSIC)
    ,
  • Autonomous University of Madrid
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 979-987 (9 pages)

Journal (Volume, Issue Number)

Journal of Alzheimer's Disease (Volume 69, Issue 4)

Publication milestones

  • Published - 2019

Publication status

Published - 2019

ISSN

1387-2877

Publication IDs

  • Scopus: 85067548773
  • PubMed: 31156175

Abstract

Increasing evidence supports the notion that Alzheimer's disease (AD), a condition that presents heterogeneous pathological disturbances, is also associated to perturbed metabolic function affecting insulin and insulin-like growth factor I (IGF-I). While impaired insulin activity leading to insulin resistance has been associated to AD, whether altered IGF-I function affects the disease is not entirely clear. Despite the limitations of mouse models to mimic AD pathology, we took advantage that serum IGF-I deficient mice (LID mice) present many functional perturbations present in AD, most prominently cognitive loss, which is reversed by treatment with systemic IGF-I. We analyzed whether these mice display other pathological traits that are usual co-morbidities of AD. We found that LID mice not only display cognitive disturbances, but also show altered mood and sociability, increased susceptibility to epileptiform activity, and a disturbed sleep/wake cycle. Collectively, these data suggest that reduced IGF-I activity contributes to heterogeneous deficits commonly associated to AD. We suggest that impaired IGF-I activity needs to be taken into consideration when modeling this condition.

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