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10.1007/s11357-017-9971-0

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suck abstract from ncbi


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pmid28409331      GeroScience 2017 ; 39 (2): 129-45
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  • IGF-1 has sexually dimorphic, pleiotropic, and time-dependent effects on healthspan, pathology, and lifespan #MMPMID28409331
  • Ashpole NM; Logan S; Yabluchanskiy A; Mitschelen MC; Yan H; Farley JA; Hodges EL; Ungvari Z; Csiszar A; Chen S; Georgescu C; Hubbard GB; Ikeno Y; Sonntag WE
  • GeroScience 2017[Apr]; 39 (2): 129-45 PMID28409331show ga
  • Reduced circulating levels of IGF-1 have been proposed as a conserved anti-aging mechanism that contributes to increased lifespan in diverse experimental models. However, IGF-1 has also been shown to be essential for normal development and the maintenance of tissue function late into the lifespan. These disparate findings suggest that IGF-1 may be a pleiotropic modulator of health and aging, as reductions in IGF-1 may be beneficial for one aspect of aging, but detrimental for another. We postulated that the effects of IGF-1 on tissue health and function in advanced age are dependent on the tissue, the sex of the animal, and the age at which IGF-1 is manipulated. In this study, we examined how alterations in IGF-1 levels at multiple stages of development and aging influence overall lifespan, healthspan, and pathology. Specifically, we investigated the effects of perinatal, post-pubertal, and late-adult onset IGF-1 deficiency using genetic and viral approaches in both male and female igff/f C57Bl/6 mice. Our results support the concept that IGF-1 levels early during lifespan establish the conditions necessary for subsequent healthspan and pathological changes that contribute to aging. Nevertheless, these changes are specific for each sex and tissue. Importantly, late-life IGF-1 deficiency (a time point relevant for human studies) reduces cancer risk but does not increase lifespan. Overall, our results indicate that the levels of IGF-1 during development influence late-life pathology, suggesting that IGF-1 is a developmental driver of healthspan, pathology, and lifespan.Electronic supplementary material: The online version of this article (doi:10.1007/s11357-017-9971-0) contains supplementary material, which is available to authorized users.
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