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Behav Brain Res. 2016 Jun 1;306:1-7. doi: 10.1016/j.bbr.2016.03.018. Epub 2016 Mar 10.

Short-term exposure to a diet high in fat and sugar, or liquid sugar, selectively impairs hippocampal-dependent memory, with differential impacts on inflammation.

Author information

1
Department of Pharmacology, School of Medical Sciences, UNSW Australia, UNSW Sydney, NSW 2052, Australia.
2
Department of Pharmacology, School of Medical Sciences, UNSW Australia, UNSW Sydney, NSW 2052, Australia. Electronic address: m.morris@unsw.edu.au.

Abstract

Chronic high-energy diets are known to induce obesity and impair memory; these changes have been associated with inflammation in brain areas crucial for memory. In this study, we investigated whether inflammation could also be related to diet-induced memory deficits, prior to obesity. We exposed rats to chow, chow supplemented with a 10% sucrose solution (Sugar) or a diet high in fat and sugar (Caf+Sugar) and assessed hippocampal-dependent and perirhinal-dependent memory at 1 week. Both high-energy diet groups displayed similar, selective hippocampal-dependent memory deficits despite the Caf+Sugar rats consuming 4-5 times more energy, and weighing significantly more than the other groups. Extreme weight gain and excessive energy intake are therefore not necessary for deficits in memory. Weight gain across the diet period however, was correlated with the memory deficits, even in the Chow rats. The Sugar rats had elevated expression of a number of inflammatory genes in the hippocampus and WAT compared to Chow and Caf+Sugar rats but not in the perirhinal cortex or hypothalamus. Blood glucose concentrations were also elevated in the Sugar rats, and were correlated with the hippocampal inflammatory markers. Together, these results indicate that liquid sugar can rapidly elevate markers of central and peripheral inflammation, in association with hyperglycemia, and this may be related to the memory deficits in the Sugar rats.

KEYWORDS:

Diet; Fat; Hippocampus; Inflammation; Memory; Sugar

PMID:
26970578
DOI:
10.1016/j.bbr.2016.03.018
[Indexed for MEDLINE]

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