Cargando…

A method for the efficient evaluation of substrate-based cholinesterase imaging probes for Alzheimer’s disease

Cholinesterase (ChE) enzymes have been identified as diagnostic markers for Alzheimer disease (AD). Substrate-based probes have been synthesised to detect ChEs but they have not detected changes in ChE distribution associated with AD pathology. Probes are typically screened using spectrophotometric...

Descripción completa

Detalles Bibliográficos
Autores principales: Darvesh, Sultan, Banfield, Scott, Dufour, Maeve, Forrestall, Katrina L., Maillet, Hillary, Reid, G. Andrew, Sands, Dane, Pottie, Ian R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294744/
http://dx.doi.org/10.1080/14756366.2023.2225797
_version_ 1785063256030707712
author Darvesh, Sultan
Banfield, Scott
Dufour, Maeve
Forrestall, Katrina L.
Maillet, Hillary
Reid, G. Andrew
Sands, Dane
Pottie, Ian R.
author_facet Darvesh, Sultan
Banfield, Scott
Dufour, Maeve
Forrestall, Katrina L.
Maillet, Hillary
Reid, G. Andrew
Sands, Dane
Pottie, Ian R.
author_sort Darvesh, Sultan
collection PubMed
description Cholinesterase (ChE) enzymes have been identified as diagnostic markers for Alzheimer disease (AD). Substrate-based probes have been synthesised to detect ChEs but they have not detected changes in ChE distribution associated with AD pathology. Probes are typically screened using spectrophotometric methods with pure enzyme for specificity and kinetics. However, the biochemical properties of ChEs associated with AD pathology are altered. The present work was undertaken to determine whether the Karnovsky-Roots (KR) histochemical method could be used to evaluate probes at the site of pathology. Thirty thioesters and esters were synthesised and evaluated using enzyme kinetic and KR methods. Spectrophotometric methods demonstrated all thioesters were ChE substrates, yet only a few provided staining in the brain with the KR method. Esters were ChE substrates with interactions with brain ChEs. These results suggest that the KR method may provide an efficient means to screen compounds as probes for imaging AD-associated ChEs.
format Online
Article
Text
id pubmed-10294744
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-102947442023-06-28 A method for the efficient evaluation of substrate-based cholinesterase imaging probes for Alzheimer’s disease Darvesh, Sultan Banfield, Scott Dufour, Maeve Forrestall, Katrina L. Maillet, Hillary Reid, G. Andrew Sands, Dane Pottie, Ian R. J Enzyme Inhib Med Chem Research Paper Cholinesterase (ChE) enzymes have been identified as diagnostic markers for Alzheimer disease (AD). Substrate-based probes have been synthesised to detect ChEs but they have not detected changes in ChE distribution associated with AD pathology. Probes are typically screened using spectrophotometric methods with pure enzyme for specificity and kinetics. However, the biochemical properties of ChEs associated with AD pathology are altered. The present work was undertaken to determine whether the Karnovsky-Roots (KR) histochemical method could be used to evaluate probes at the site of pathology. Thirty thioesters and esters were synthesised and evaluated using enzyme kinetic and KR methods. Spectrophotometric methods demonstrated all thioesters were ChE substrates, yet only a few provided staining in the brain with the KR method. Esters were ChE substrates with interactions with brain ChEs. These results suggest that the KR method may provide an efficient means to screen compounds as probes for imaging AD-associated ChEs. Taylor & Francis 2023-06-26 /pmc/articles/PMC10294744/ http://dx.doi.org/10.1080/14756366.2023.2225797 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Paper
Darvesh, Sultan
Banfield, Scott
Dufour, Maeve
Forrestall, Katrina L.
Maillet, Hillary
Reid, G. Andrew
Sands, Dane
Pottie, Ian R.
A method for the efficient evaluation of substrate-based cholinesterase imaging probes for Alzheimer’s disease
title A method for the efficient evaluation of substrate-based cholinesterase imaging probes for Alzheimer’s disease
title_full A method for the efficient evaluation of substrate-based cholinesterase imaging probes for Alzheimer’s disease
title_fullStr A method for the efficient evaluation of substrate-based cholinesterase imaging probes for Alzheimer’s disease
title_full_unstemmed A method for the efficient evaluation of substrate-based cholinesterase imaging probes for Alzheimer’s disease
title_short A method for the efficient evaluation of substrate-based cholinesterase imaging probes for Alzheimer’s disease
title_sort method for the efficient evaluation of substrate-based cholinesterase imaging probes for alzheimer’s disease
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294744/
http://dx.doi.org/10.1080/14756366.2023.2225797
work_keys_str_mv AT darveshsultan amethodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT banfieldscott amethodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT dufourmaeve amethodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT forrestallkatrinal amethodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT maillethillary amethodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT reidgandrew amethodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT sandsdane amethodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT pottieianr amethodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT darveshsultan methodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT banfieldscott methodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT dufourmaeve methodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT forrestallkatrinal methodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT maillethillary methodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT reidgandrew methodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT sandsdane methodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease
AT pottieianr methodfortheefficientevaluationofsubstratebasedcholinesteraseimagingprobesforalzheimersdisease