Premium
Blueberry Supplementation Attenuates Inflammation and Oxidative Stress and Increases Brain‐Derived Neurotrophic Factor in the Brains of Middle‐Aged Mice Consuming a High Fat Diet
Author(s) -
Carey Amanda,
Gildawie Kelsea,
Gilman Casey,
Rovnak Abigail,
ShukittHale Barbara
Publication year - 2015
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.29.1_supplement.lb270
Subject(s) - endocrinology , oxidative stress , medicine , neurotrophic factors , brain derived neurotrophic factor , tumor necrosis factor alpha , hippocampal formation , inflammation , calorie , hippocampus , cytokine , cerebral cortex , chemistry , biology , receptor
Previously it was demonstrated that 9 month old mice fed a high fat diet (HFD, Harlan, TD.06414, 60% calories from lard fat) for five months had impaired memory; however supplementation of the HFD with 4% blueberry (BB, freeze‐dried extract, U.S. Highbush Blueberry Council) reduced these memory deficits. The brains of these mice were dissected, homogenized, and assayed with ELISA for brain‐derived neurotrophic factor (BDNF), the inflammatory cytokine tumor necrosis factor (TNF)‐alpha, and were evaluated for oxidative stress by examining 4‐Hydroxynonenal (4‐HNE). There was a significant increase in hippocampal BDNF in the animals fed the HFD + BB (273±56 pg/ml/per mg of tissue) in comparison with the low fat diet (LFD, TD.08806, 10% calories from fat) and HFD‐fed animals without BB supplementation (44±3 and 46±2 pg/ml, respectively). There was also a trend suggesting that animals fed a LFD + BB had elevated BDNF levels (101±57 pg/ml). Greater levels of TNF‐alpha were found in the cerebral cortex of mice fed a HFD compared to mice fed a LFD, and there was a partial reduction of TNF‐alpha in mice fed HFD + BB. 4‐HNE was found to be elevated in the cortex of mice fed a HFD compared to the mice that had BB supplementation in the HFD. This study attempts to determine the pathways and molecules that HFD consumption modulates that may underlie the previously demonstrated memory impairment, and also to begin to elucidate the mechanisms by which blueberry supplementation mediates these changes. Supported by U.S. Highbush Blueberry Council