Effect of high-fat diet on metabolic indices, cognition, and neuronal physiology in aging F344 rats

Tristano Pancani, Katie L. Anderson, Lawrence D. Brewer, Inga Kadish, Chris DeMoll, Philip W. Landfield, Eric M. Blalock, Nada M. Porter, Olivier Thibault

Producción científica: Articlerevisión exhaustiva

71 Citas (Scopus)

Resumen

The prevalence of obesity and type 2 diabetes increases with age. Despite this, few studies have examined these conditions simultaneously in aged animals, and fewer studies have measured the impact of these conditions on brain function. Using an established animal model of brain aging (F344 rats), we investigated whether a high-fat diet (HFD) exacerbates cognitive decline and the hippocampal calcium-dependent afterhyperpolarization (a marker of age-dependent calcium dysregulation). Young and mid-aged animals were maintained on control or HFD for 4.5 months, and peripheral metabolic variables, cognitive function, and electrophysiological responses to insulin in the hippocampus were measured. HFD increased lipid accumulation in the periphery, although overt diabetes did not develop, nor were spatial learning and memory altered. Hippocampal adiponectin levels were reduced in aging animals but were unaffected by HFD. For the first time, however, we show that the AHP is sensitive to insulin, and that this sensitivity is reduced by HFD. Interestingly, although peripheral glucose regulation was relatively insensitive to HFD, the brain appeared to show greater sensitivity to HFD in F344 rats.

Idioma originalEnglish
Páginas (desde-hasta)1977-1987
Número de páginas11
PublicaciónNeurobiology of Aging
Volumen34
N.º8
DOI
EstadoPublished - ago 2013

Nota bibliográfica

Funding Information:
This work was supported by National Institutes of Health (NIH)/National Institute on Aging (NIA) grant AG033649 . The authors thank Drs. Hadley and Piascik for critical reading and reviewing of the manuscript.

Financiación

This work was supported by National Institutes of Health (NIH)/National Institute on Aging (NIA) grant AG033649 . The authors thank Drs. Hadley and Piascik for critical reading and reviewing of the manuscript.

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)
National Institute on AgingAG033649, R01AG037868

    ASJC Scopus subject areas

    • General Neuroscience
    • Aging
    • Clinical Neurology
    • Developmental Biology
    • Geriatrics and Gerontology

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