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A safe, blood-brain barrier permeable triphenylmethane dye inhibits amyloid-β neurotoxicity by generating nontoxic aggregates.
ACS Chem Neurosci 2011; 2(11):645-57AC

Abstract

Growing evidence suggests that on-pathway amyloid-β (Aβ) oligomers are primary neurotoxic species and have a direct correlation with the onset of Alzheimer's disease (AD). One promising therapeutic strategy to block AD progression is to reduce the levels of these neurotoxic Aβ species using small molecules. While several compounds have been shown to modulate Aβ aggregation, compounds with such activity combined with safety and high blood-brain barrier (BBB) permeability have yet to be reported. Brilliant Blue G (BBG) is a close structural analogue of a U.S. Food and Drug Administration (FDA)-approved food dye and has recently garnered prominent attention as a potential drug to treat spinal cord injury due to its neuroprotective effects along with BBB permeability and high degree of safety. In this work, we demonstrate that BBG is an effective Aβ aggregation modulator, which reduces Aβ-associated cytotoxicity in a dose-dependent manner by promoting the formation of off-pathway, nontoxic aggregates. Comparative studies of BBG and three structural analogues, Brilliant Blue R (BBR), Brilliant Blue FCF (BBF), and Fast Green FCF (FGF), revealed that BBG is most effective, BBR is moderately effective, and BBF and FGF are least effective in modulating Aβ aggregation and cytotoxicity. Therefore, the two additional methyl groups of BBG and other structural differences between the congeners are important in the interaction of BBG with Aβ leading to formation of nontoxic Aβ aggregates. Our findings support the hypothesis that generating nontoxic aggregates using small molecule modulators is an effective strategy for reducing Aβ cytotoxicity. Furthermore, key structural features of BBG identified through structure-function studies can open new avenues into therapeutic design for combating AD.

Authors+Show Affiliations

Department of Chemical Engineering, University of Virginia, Charlottesville, Virginia 22911, USA.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

22860159

Citation

Wong, H Edward, et al. "A Safe, Blood-brain Barrier Permeable Triphenylmethane Dye Inhibits Amyloid-β Neurotoxicity By Generating Nontoxic Aggregates." ACS Chemical Neuroscience, vol. 2, no. 11, 2011, pp. 645-57.
Wong HE, Qi W, Choi HM, et al. A safe, blood-brain barrier permeable triphenylmethane dye inhibits amyloid-β neurotoxicity by generating nontoxic aggregates. ACS Chem Neurosci. 2011;2(11):645-57.
Wong, H. E., Qi, W., Choi, H. M., Fernandez, E. J., & Kwon, I. (2011). A safe, blood-brain barrier permeable triphenylmethane dye inhibits amyloid-β neurotoxicity by generating nontoxic aggregates. ACS Chemical Neuroscience, 2(11), pp. 645-57. doi:10.1021/cn200056g.
Wong HE, et al. A Safe, Blood-brain Barrier Permeable Triphenylmethane Dye Inhibits Amyloid-β Neurotoxicity By Generating Nontoxic Aggregates. ACS Chem Neurosci. 2011 Nov 16;2(11):645-57. PubMed PMID: 22860159.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A safe, blood-brain barrier permeable triphenylmethane dye inhibits amyloid-β neurotoxicity by generating nontoxic aggregates. AU - Wong,H Edward, AU - Qi,Wei, AU - Choi,Hyung-Min, AU - Fernandez,Erik J, AU - Kwon,Inchan, Y1 - 2011/09/06/ PY - 2011/06/12/received PY - 2011/09/06/accepted PY - 2012/8/4/entrez PY - 2012/8/4/pubmed PY - 2012/8/4/medline KW - Alzheimer’s disease KW - Brilliant blue KW - amyloid-β KW - fibrils KW - nontoxic aggregates KW - oligomers SP - 645 EP - 57 JF - ACS chemical neuroscience JO - ACS Chem Neurosci VL - 2 IS - 11 N2 - Growing evidence suggests that on-pathway amyloid-β (Aβ) oligomers are primary neurotoxic species and have a direct correlation with the onset of Alzheimer's disease (AD). One promising therapeutic strategy to block AD progression is to reduce the levels of these neurotoxic Aβ species using small molecules. While several compounds have been shown to modulate Aβ aggregation, compounds with such activity combined with safety and high blood-brain barrier (BBB) permeability have yet to be reported. Brilliant Blue G (BBG) is a close structural analogue of a U.S. Food and Drug Administration (FDA)-approved food dye and has recently garnered prominent attention as a potential drug to treat spinal cord injury due to its neuroprotective effects along with BBB permeability and high degree of safety. In this work, we demonstrate that BBG is an effective Aβ aggregation modulator, which reduces Aβ-associated cytotoxicity in a dose-dependent manner by promoting the formation of off-pathway, nontoxic aggregates. Comparative studies of BBG and three structural analogues, Brilliant Blue R (BBR), Brilliant Blue FCF (BBF), and Fast Green FCF (FGF), revealed that BBG is most effective, BBR is moderately effective, and BBF and FGF are least effective in modulating Aβ aggregation and cytotoxicity. Therefore, the two additional methyl groups of BBG and other structural differences between the congeners are important in the interaction of BBG with Aβ leading to formation of nontoxic Aβ aggregates. Our findings support the hypothesis that generating nontoxic aggregates using small molecule modulators is an effective strategy for reducing Aβ cytotoxicity. Furthermore, key structural features of BBG identified through structure-function studies can open new avenues into therapeutic design for combating AD. SN - 1948-7193 UR - https://www.unboundmedicine.com/medline/citation/22860159/A_safe_blood_brain_barrier_permeable_triphenylmethane_dye_inhibits_amyloid_β_neurotoxicity_by_generating_nontoxic_aggregates_ L2 - https://dx.doi.org/10.1021/cn200056g DB - PRIME DP - Unbound Medicine ER -