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Exp Gerontol ; 68: 76-81, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25300732

ABSTRACT

Growth hormone (GH) and insulin-like growth factor (IGF)-1 regulate the development and function of cells throughout the body. Several clinical diseases that result in a decline in physical and mental functions are marked by mutations that disrupt GH or IGF-1 signaling. During the lifespan there is a robust decrease in both GH and IGF-1. Because GH and IGF-1 are master regulators of cellular function, impaired GH and IGF-1 signaling in aging/disease states leads to significant alterations in tissue structure and function, especially within the brain. This review is intended to highlight the effects of the GH and IGF-1 on neuronal structure, function, and plasticity. Furthermore, we address several potential mechanisms through which the age-related reductions in GH and IGF-1 affect cognition. Together, the studies reviewed here highlight the importance of maintaining GH and IGF-1 signaling in order to sustain proper brain function throughout the lifespan.


Subject(s)
Aging/physiology , Brain/physiology , Growth Hormone/physiology , Insulin-Like Growth Factor I/physiology , Adolescent , Adult , Aging/metabolism , Animals , Brain/growth & development , Brain/metabolism , Child , Growth Hormone/metabolism , Growth Hormone/pharmacology , Human Growth Hormone/deficiency , Human Growth Hormone/metabolism , Human Growth Hormone/physiology , Humans , Insulin-Like Growth Factor I/metabolism , Mice , Models, Biological , Neuronal Plasticity/physiology , Rats , Receptors, N-Methyl-D-Aspartate/physiology , Signal Transduction/physiology
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