Unravelling Novel Phytochemicals and Anticholinesterase Activity in Irish Cladonia portentosa

Acetylcholinesterase inhibitors remain the mainstay of symptomatic treatment for Alzheimer’s disease. The natural world is rich in acetylcholinesterase inhibitory molecules, and research efforts to identify novel leads is ongoing. Cladonia portentosa, commonly known as reindeer lichen, is an abundan...

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Published in:Molecules
Main Authors: Nagar, Shipra, Pigott, Maria, Kukula-Koch, Wirginia, Sheridan, Helen
Format: Text
Language:English
Published: MDPI 2023
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222842/
http://www.ncbi.nlm.nih.gov/pubmed/37241886
https://doi.org/10.3390/molecules28104145
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spelling ftpubmed:oai:pubmedcentral.nih.gov:10222842 2023-06-18T03:42:51+02:00 Unravelling Novel Phytochemicals and Anticholinesterase Activity in Irish Cladonia portentosa Nagar, Shipra Pigott, Maria Kukula-Koch, Wirginia Sheridan, Helen 2023-05-17 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222842/ http://www.ncbi.nlm.nih.gov/pubmed/37241886 https://doi.org/10.3390/molecules28104145 en eng MDPI http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222842/ http://www.ncbi.nlm.nih.gov/pubmed/37241886 http://dx.doi.org/10.3390/molecules28104145 © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Molecules Article Text 2023 ftpubmed https://doi.org/10.3390/molecules28104145 2023-06-04T01:06:07Z Acetylcholinesterase inhibitors remain the mainstay of symptomatic treatment for Alzheimer’s disease. The natural world is rich in acetylcholinesterase inhibitory molecules, and research efforts to identify novel leads is ongoing. Cladonia portentosa, commonly known as reindeer lichen, is an abundant lichen species found in Irish Boglands. The methanol extract of Irish C. portentosa was identified as an acetylcholinesterase inhibitory lead using qualitative TLC-bioautography in a screening program. To identify the active components, the extract was deconvoluted using a successive extraction process with hexane, ethyl acetate and methanol to isolate the active fraction. The hexane extract demonstrated the highest inhibitory activity and was selected for further phytochemical investigations. Olivetolic acid, 4-O-methylolivetolcarboxylic acid, perlatolic acid and usnic acid were isolated and characterized using ESI-MS and two-dimensional NMR techniques. LC-MS analysis also determined the presence of the additional usnic acid derivatives, placodiolic and pseudoplacodiolic acids. Assays of the isolated components confirmed that the observed anticholinesterase activity of C. portentosa can be attributed to usnic acid (25% inhibition at 125 µM) and perlatolic acid (20% inhibition at 250 µM), which were both reported inhibitors. This is the first report of isolation of olivetolic and 4-O-methylolivetolcarboxylic acids and the identification of placodiolic and pseudoplacodiolic acids from C. portentosa. Text Reindeer lichen PubMed Central (PMC) Molecules 28 10 4145
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Article
spellingShingle Article
Nagar, Shipra
Pigott, Maria
Kukula-Koch, Wirginia
Sheridan, Helen
Unravelling Novel Phytochemicals and Anticholinesterase Activity in Irish Cladonia portentosa
topic_facet Article
description Acetylcholinesterase inhibitors remain the mainstay of symptomatic treatment for Alzheimer’s disease. The natural world is rich in acetylcholinesterase inhibitory molecules, and research efforts to identify novel leads is ongoing. Cladonia portentosa, commonly known as reindeer lichen, is an abundant lichen species found in Irish Boglands. The methanol extract of Irish C. portentosa was identified as an acetylcholinesterase inhibitory lead using qualitative TLC-bioautography in a screening program. To identify the active components, the extract was deconvoluted using a successive extraction process with hexane, ethyl acetate and methanol to isolate the active fraction. The hexane extract demonstrated the highest inhibitory activity and was selected for further phytochemical investigations. Olivetolic acid, 4-O-methylolivetolcarboxylic acid, perlatolic acid and usnic acid were isolated and characterized using ESI-MS and two-dimensional NMR techniques. LC-MS analysis also determined the presence of the additional usnic acid derivatives, placodiolic and pseudoplacodiolic acids. Assays of the isolated components confirmed that the observed anticholinesterase activity of C. portentosa can be attributed to usnic acid (25% inhibition at 125 µM) and perlatolic acid (20% inhibition at 250 µM), which were both reported inhibitors. This is the first report of isolation of olivetolic and 4-O-methylolivetolcarboxylic acids and the identification of placodiolic and pseudoplacodiolic acids from C. portentosa.
format Text
author Nagar, Shipra
Pigott, Maria
Kukula-Koch, Wirginia
Sheridan, Helen
author_facet Nagar, Shipra
Pigott, Maria
Kukula-Koch, Wirginia
Sheridan, Helen
author_sort Nagar, Shipra
title Unravelling Novel Phytochemicals and Anticholinesterase Activity in Irish Cladonia portentosa
title_short Unravelling Novel Phytochemicals and Anticholinesterase Activity in Irish Cladonia portentosa
title_full Unravelling Novel Phytochemicals and Anticholinesterase Activity in Irish Cladonia portentosa
title_fullStr Unravelling Novel Phytochemicals and Anticholinesterase Activity in Irish Cladonia portentosa
title_full_unstemmed Unravelling Novel Phytochemicals and Anticholinesterase Activity in Irish Cladonia portentosa
title_sort unravelling novel phytochemicals and anticholinesterase activity in irish cladonia portentosa
publisher MDPI
publishDate 2023
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222842/
http://www.ncbi.nlm.nih.gov/pubmed/37241886
https://doi.org/10.3390/molecules28104145
genre Reindeer lichen
genre_facet Reindeer lichen
op_source Molecules
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222842/
http://www.ncbi.nlm.nih.gov/pubmed/37241886
http://dx.doi.org/10.3390/molecules28104145
op_rights © 2023 by the authors.
https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
op_doi https://doi.org/10.3390/molecules28104145
container_title Molecules
container_volume 28
container_issue 10
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