pubmed-article:20454453 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20454453 | lifeskim:mentions | umls-concept:C0001811 | lld:lifeskim |
pubmed-article:20454453 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
pubmed-article:20454453 | lifeskim:mentions | umls-concept:C1280500 | lld:lifeskim |
pubmed-article:20454453 | lifeskim:mentions | umls-concept:C0071097 | lld:lifeskim |
pubmed-article:20454453 | lifeskim:mentions | umls-concept:C0205100 | lld:lifeskim |
pubmed-article:20454453 | lifeskim:mentions | umls-concept:C2745888 | lld:lifeskim |
pubmed-article:20454453 | lifeskim:mentions | umls-concept:C0205099 | lld:lifeskim |
pubmed-article:20454453 | lifeskim:mentions | umls-concept:C0443252 | lld:lifeskim |
pubmed-article:20454453 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:20454453 | pubmed:dateCreated | 2010-5-10 | lld:pubmed |
pubmed-article:20454453 | pubmed:abstractText | Thiazolidinediones (TZDs) activate peroxisome proliferator-activated receptor gamma (PPARgamma) and are used clinically to help restore peripheral insulin sensitivity in Type 2 diabetes (T2DM). Interestingly, long-term treatment of mouse models of Alzheimer's disease (AD) with TZDs also has been shown to reduce several well-established brain biomarkers of AD including inflammation, oxidative stress and Abeta accumulation. While TZD's actions in AD models help to elucidate the mechanisms underlying their potentially beneficial effects in AD patients, little is known about the functional consequences of TZDs in animal models of normal aging. Because aging is a common risk factor for both AD and T2DM, we investigated whether the TZD, pioglitazone could alter brain aging under non-pathological conditions. | lld:pubmed |
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