Literature DB >> 17279347

Properties of scyllo-inositol as a therapeutic treatment of AD-like pathology.

Daniela Fenili1, Mary Brown, Rebecca Rappaport, JoAnne McLaurin.   

Abstract

Inositol is a simple polyol with eight naturally occurring stereoisomers. myo-Inositol, D-chiro- and epi-inositol have been examined as potential therapeutic agents for various diseases, with favorable results, but treatment with scyllo-inositol has not been previously investigated. Our laboratory has shown that scyllo-inositol inhibits cognitive deficits in TgCRND8 mice and significantly ameliorates disease pathology, suggesting it might be effective in treating Alzheimer's disease (AD). In this paper, we show that scyllo-inositol has a sustained ability to treat animals at advanced stages of AD-like pathology. Significant decreases in insoluble Abeta40, Abeta42, and plaque accumulation were observed in the brains of treated versus untreated TgCRND8 mice. The growth of plaques of all sizes was inhibited by scyllo-inositol administration. To demonstrate that the scyllo-inositol effects were within the CNS, gas chromatography/mass spectrometry was used to examine myo- and scyllo-inositol concentrations after oral administration. Further, we examined how closely scyllo- and myo-inositol are inter-regulated in the CNS and whether scyllo-inositol, if elevated within the CNS, would incorporate into phosphatidylinositol lipids. Cerebral spinal fluid levels of scyllo-inositol increased after scyllo-inositol treatment but not myo-inositol treatment. scyllo-Inositol treatment also caused increased levels of scyllo-inositol in the brain. We further show that scyllo-inositol, even at elevated levels, does not incorporate into the phosphatidylinositol family of lipids. These combined results demonstrate that scyllo-inositol accumulates within the CNS up to tenfold endogenous levels and does not interfere with phosphatidylinositol lipid production.

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Year:  2007        PMID: 17279347     DOI: 10.1007/s00109-007-0156-7

Source DB:  PubMed          Journal:  J Mol Med (Berl)        ISSN: 0946-2716            Impact factor:   5.606


  48 in total

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2.  Epi-inositol is biochemically active in reversing lithium effects on cytidine monophosphorylphosphatidate (CMP-PA). Short communication.

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3.  A beta peptide immunization reduces behavioural impairment and plaques in a model of Alzheimer's disease.

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Journal:  NMR Biomed       Date:  2005-02       Impact factor: 4.044

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Journal:  J Mol Cell Cardiol       Date:  1993-06       Impact factor: 5.000

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  29 in total

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Authors:  Mark P Thomas; Stephen J Mills; Barry V L Potter
Journal:  Angew Chem Int Ed Engl       Date:  2015-12-22       Impact factor: 15.336

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Journal:  Appl Environ Microbiol       Date:  2010-10-22       Impact factor: 4.792

3.  Combination therapy in a transgenic model of Alzheimer's disease.

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4.  A phase 2 randomized trial of ELND005, scyllo-inositol, in mild to moderate Alzheimer disease.

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Review 5.  Vitamins Associated with Brain Aging, Mild Cognitive Impairment, and Alzheimer Disease: Biomarkers, Epidemiological and Experimental Evidence, Plausible Mechanisms, and Knowledge Gaps.

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Review 6.  Improving Memory and Cognition in Individuals with Down Syndrome.

Authors:  Michael S Rafii
Journal:  CNS Drugs       Date:  2016-07       Impact factor: 5.749

7.  scyllo-Inositol promotes robust mutant Huntingtin protein degradation.

Authors:  Aaron Y Lai; Cynthia P Lan; Salwa Hasan; Mary E Brown; Joanne McLaurin
Journal:  J Biol Chem       Date:  2013-12-18       Impact factor: 5.157

Review 8.  Amyloid beta-protein assembly as a therapeutic target of Alzheimer's disease.

Authors:  Ghiam Yamin; Kenjiro Ono; Mohammed Inayathullah; David B Teplow
Journal:  Curr Pharm Des       Date:  2008       Impact factor: 3.116

9.  Consumption of pasteurized human lysozyme transgenic goats' milk alters serum metabolite profile in young pigs.

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10.  Protection against the synaptic targeting and toxicity of Alzheimer's-associated Aβ oligomers by insulin mimetic chiro-inositols.

Authors:  Jason Pitt; Michael Thorner; David Brautigan; Joseph Larner; William L Klein
Journal:  FASEB J       Date:  2012-10-16       Impact factor: 5.191

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