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In a recent clinical study, the thiazolidinedione (TZD) pioglitazone (Actos was reported to preserve cognitive function in patients with mild to moderate Alzheimer's disease and type II diabetes mellitus. TZDs are agonists of the nuclear hormone receptor peroxisome proliferator-activated receptor-gamma (PPARgamma), are peripheral insulin sensitizers, and have recently been reported to increase mitochondrial biogenesis in the central nervous system and dendritic spine density. We report a transcriptional profile of the TZD pioglitazone and the non-TZD PPARgamma agonist GW347845 in primary cortical culture. We observed that pioglitazone, but not GW347845, increased cholesterol biosynthetic and lipogenic gene expression after 6 h, and the expression of the cholesterol efflux transporters Abca1 and Abcg1 after 24 h. Co-treatment of pioglitazone with the PPARgamma antagonist GW9662 did not significantly reduce these effects, suggesting a PPARgamma-independent mechanism. These findings suggest a novel effect of TZDs in neurons that may be of relevance as a novel approach against Alzheimer's disease.

Original publication

DOI

10.3233/JAD-2010-1266

Type

Journal article

Journal

J Alzheimers Dis

Publication Date

2010

Volume

19

Pages

631 - 646

Keywords

Animals, Cells, Cultured, Cerebral Cortex, Cholesterol, Embryo, Mammalian, Enzyme Inhibitors, Gene Expression Profiling, Hypoglycemic Agents, Neurons, Oligonucleotide Array Sequence Analysis, PPAR gamma, Rats, Rats, Sprague-Dawley, Sterol Regulatory Element Binding Protein 1, Thiazolidinediones, Time Factors, Up-Regulation