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BChE inhibitors from marine organisms - A review

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CHEMICO-BIOLOGICAL INTERACTIONS
卷 367, 期 -, 页码 -

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ELSEVIER IRELAND LTD
DOI: 10.1016/j.cbi.2022.110136

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Cholinesterase inhibitors; Butyrylcholinesterase inhibitors; Marine natural products

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This article discusses the research progress on the decreased levels of acetylcholine in Alzheimer's Disease and the development of selective butyrylcholinesterase inhibitors as a potential strategy. The article also highlights the marine environment as a rich source of therapeutic molecules with reduced toxicity risks compared to synthetic molecules. Some marine compounds show excellent potential for butyrylcholinesterase inhibition.
Acetylcholine is a key neurotransmitter for brain and muscle function, that has its levels decreased in the brain of people with Alzheimer's Disease (AD). Cholinesterase inhibitors are medicines that decrease the breakdown of acetylcholine, through the inhibition of acetyl-and butyrylcholinesterase enzymes. Despite the fact that butyr-ylcholinesterase activity rises with the disease, while acetylcholinesterase activity declines, the cholinesterase inhibitors that are currently commercialized inhibit either acetylcholinesterase or both enzymes. The develop-ment of selective butyrylcholinesterase inhibitors is a promising strategy in the search for new drugs acting against AD. The marine environment is a rich source of molecules with therapeutic potential, which can provide compounds more easily than traditional methods, with reduced toxicity risks compared to synthetic molecules. This review comprises articles from 2003 to 2020, that assessed the butyrylcholinesterase inhibitory activities from marine organisms, considering their crude extracts and isolated compounds. Part of the articles reported a multi-target activity, inhibiting also other AD-related enzymes. Some of the marine compounds reported here have shown an excellent potential for butyrylcholinesterase inhibition compared to standard inhibitors. Further studies of some compounds reported here may lead to the development of a new treatment for AD.

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