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Title

Role of serum insulin-like growth factor I in mammalian brain aging

AuthorsTrejo, José L. ; Carro, Eva; López-López, C.; Torres Alemán, Ignacio
Issue Date2004
PublisherChurchill Livingstone
CitationGrowth Hormone and IGF Research 14: S39- S43 (2004)
AbstractModern societies face new public health challenges associated with an increasingly aging population. Among these, pathological conditions linked to brain aging are paramount. Old age is a risk factor for important neurological impairments such as Alzheimer's disease or stroke. Even healthy elderly people usually present with milder forms of cognitive decline. This is possibly related to less-pronounced brain deficits seen in normal aging, including the shrinkage of neurons and the dense network of neurons and glia in the central nervous system known as the neuropil, a lower neurogenetic rate, impaired angiogenesis or brain accumulation of deleterious compounds. At least in mammals, age is also associated with a decline in insulin-like growth factor-I (IGF-I) levels, a well-known neuroprotective agent. Recently, a relationship between serum IGF-I and >house-keeping> mechanisms in the brain has been evidenced in laboratory rodents. Serum IGF-I increases adult neurogenesis, sustains neuronal health through a variety of fundamental homeostatic mechanisms, participates in brain angiogenesis, contributes to brain β-amyloid clearance and affects learning and memory. Overall, diminished trophic input resulting from decreasing serum IGF-I levels during aging likely contributes to brain senescence in mammals. © 2004 Elsevier Ltd. All rights reserved.
URIhttp://hdl.handle.net/10261/60893
DOI10.1016/j.ghir.2004.03.010
ISSN1096-6374
Appears in Collections:(IC) Artículos
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