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)
- ,
- Facultad de Medicina de la Universidad Nacional de San Agustín,
- Instituto de Salud Carlos III,
- Cajal Institute (CSIC),
- Autonomous University of Madrid
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Publication Information
Output type
Original language
EnglishPages 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
ISSN
1387-2877Publication 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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