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Publication : Synergistic neuroprotection by coffee components eicosanoyl-5-hydroxytryptamide and caffeine in models of Parkinson's disease and DLB.

First Author  Yan R Year  2018
Journal  Proc Natl Acad Sci U S A Volume  115
Issue  51 Pages  E12053-E12062
PubMed ID  30509990 Mgi Jnum  J:269264
Mgi Id  MGI:6272187 Doi  10.1073/pnas.1813365115
Citation  Yan R, et al. (2018) Synergistic neuroprotection by coffee components eicosanoyl-5-hydroxytryptamide and caffeine in models of Parkinson's disease and DLB. Proc Natl Acad Sci U S A 115(51):E12053-E12062
abstractText  Hyperphosphorylated alpha-synuclein in Lewy bodies and Lewy neurites is a characteristic neuropathological feature of Parkinson's disease (PD) and Dementia with Lewy bodies (DLB). The catalytic subunit of the specific phosphatase, protein phosphatase 2A (PP2A) that dephosphorylates alpha-synuclein, is hypomethylated in these brains, thereby impeding the assembly of the active trimeric holoenzyme and reducing phosphatase activity. This phosphatase deficiency contributes to the accumulation of hyperphosphorylated alpha-synuclein, which tends to fibrillize more than unmodified alpha-synuclein. Eicosanoyl-5-hydroxytryptamide (EHT), a fatty acid derivative of serotonin found in coffee, inhibits the PP2A methylesterase so as to maintain PP2A in a highly active methylated state and mitigates the phenotype of alpha-synuclein transgenic (Syn(Tg)) mice. Considering epidemiologic and experimental evidence suggesting protective effects of caffeine in PD, we sought, in the present study, to test whether there is synergy between EHT and caffeine in models of alpha-synucleinopathy. Coadministration of these two compounds orally for 6 mo at doses that were individually ineffective in Syn(Tg) mice and in a striatal alpha-synuclein preformed fibril inoculation model resulted in reduced accumulation of phosphorylated alpha-synuclein, preserved neuronal integrity and function, diminished neuroinflammation, and improved behavioral performance. These indices were associated with increased levels of methylated PP2A in brain tissue. A similar profile of greater PP2A methylation and cytoprotection was found in SH-SY5Y cells cotreated with EHT and caffeine, but not with each compound alone. These findings suggest that these two components of coffee have synergistic effects in protecting the brain against alpha-synuclein-mediated toxicity through maintenance of PP2A in an active state.
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