Garcinoic acid prevents ?-amyloid (A?) deposition in the mouse brain.

ABSTRACT: Garcinoic acid (GA or ?-T3-13'COOH), is a natural vitamin E metabolite that has preliminarily been identified as a modulator of nuclear receptors involved in ?-amyloid (A?) metabolism and progression of Alzheimer's disease (AD). In this study, we investigated GA's effects on A? oligomer formation and deposition. Specifically, we compared them with those of other vitamin E analogs and the soy isoflavone genistein, a natural agonist of peroxisome proliferator-activated receptor ? (PPAR?) that has therapeutic potential for managing AD. GA significantly reduced A? aggregation and accumulation in mouse cortical astrocytes. Similarly to genistein, GA up-regulated PPAR? expression and apolipoprotein E (ApoE) efflux in these cells with an efficacy that was comparable with that of its metabolic precursor ?-tocotrienol and higher than those of ?-tocopherol metabolites. Unlike for genistein and the other vitamin E compounds, the GA-induced restoration of ApoE efflux was not affected by pharmacological inhibition of PPAR? activity, and specific activation of pregnane X receptor (PXR) was observed together with ApoE and multidrug resistance protein 1 (MDR1) membrane transporter up-regulation in both the mouse astrocytes and brain tissue. These effects of GA were associated with reduced A? deposition in the brain of TgCRND8 mice, a transgenic AD model. In conclusion, GA holds potential for preventing A? oligomerization and deposition in the brain. The mechanistic aspects of GA's properties appear to be distinct from those of other vitamin E metabolites and of genistein.

SUBMITTER: Marinelli R 

PROVIDER: S-EPMC7450134 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature