Despite the advent of new treatment strategies, cholinesterase inhibitors (ChEIs) are still the go-to treatment for dementia disorders. ChEIs act by inhibiting the main acetylcholine-degrading enzyme, acetylcholinesterase (AChE). Nonetheless, accumulating evidence indicates that the impact of inhibition of the sister enzyme, butyrylcholinesterase (BChE), could be even broader in older adults due to the multifaceted role of BChE in several biological functional pathways. Therefore, we employed an modeling-based drug repurposing strategy to identify novel potent BChE inhibitors from the FDA drug database. This was followed by screening and enzyme kinetic validation using human plasma samples as the source of BChE. The analysis revealed that the antidepressant drug, duloxetine, inhibited BChE with high selectivity in comparison to AChE. In contrast, two other antidepressants, namely, citalopram and escitalopram exhibited a weak to moderate activity. enzyme inhibition kinetic analyses indicated that duloxetine acted as a competitive inhibitor of BChE with an inhibition constant ( ) of 210 nM. This value is comparable with 100-400 nM concentration of duloxetine following normal dosages in humans, thereby indicating that duloxetine should be able to induce a pharmacologically and biologically relevant inhibition of BChE. Additionally, we performed the enzyme inhibition kinetic assessment in parallel for ethopropazine, a known potent selective BChE inhibitor, and physostigmine, a dual inhibitor of AChE and BChE. These analyses indicated that duloxetine should be considered a potent BChE inhibitor since its was comparable with ethopropazine ( = 150 nM) but was 4 times smaller than that of physostigmine ( 840 nM). In conclusion, this study reports the discovery of duloxetine being a highly potent selective competitive BChE inhibitor. This, in turn, indicates that duloxetine could be the choice of antidepressive treatment in older adults with both depressive and dementia symptoms since it may offer additional clinically beneficial effects this secondary mode of cholinergic enhancing action.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11375813PMC
http://dx.doi.org/10.1021/acsomega.4c05089DOI Listing

Publication Analysis

Top Keywords

bche inhibitor
12
bche
11
cholinergic enhancing
8
older adults
8
potent bche
8
enzyme inhibition
8
inhibition kinetic
8
analyses indicated
8
indicated duloxetine
8
potent selective
8

Similar Publications

Plant-derived bioactive substances have demonstrated significant qualities that suggest they may be crucial in preventing various chronic diseases. Flavonoids, which include apigenin, are the biggest group of polyphenols. In our study, we aimed to obtain the methanol-chloroform (1:1) extract from the aerial parts of Hedge & Lamond and purify the apigenin using bioactivity-guided isolation to separate the active fraction.

View Article and Find Full Text PDF

New conjugates of amiridine and salicylic derivatives (salicylamide, salicylimine, and salicylamine) with different lengths of alkylene spacers were designed, synthesized, and evaluated as potential multifunctional central nervous system therapeutic agents for Alzheimer's disease (AD). Conjugates demonstrated high acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibition (IC: AChE, 0.265-4.

View Article and Find Full Text PDF

Optimization and Chemical Characterization of Extracts Obtained from var. Aerial Parts and Roots and Their Neuroprotective Evaluation.

Nutrients

December 2024

Foodomics Laboratory, Instituto de Investigacion en Ciencias de la Alimentacion (CIAL), Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid (CSIC-UAM), Nicolas Cabrera 9, 28049 Madrid, Spain.

Background/objectives: The genus has been traditionally used for the treatment of various illnesses, but the potential of var. against different Alzheimer's disease (AD) hallmarks has never been achieved.

Methods: In this work, a pressurized liquid extraction (PLE) method was optimized to extract L.

View Article and Find Full Text PDF

The study aimed to investigate 12 novel thiazole compounds in the treatment of neurodegenerative disorders. The compounds produced were evaluated for their inhibitory efficacy against acetylcholinesterase (AChE), butyrylcholinesterase (BChE), and monoamine oxidases (MAOs). Among the compounds, , , and showed the highest AChE inhibitory activity.

View Article and Find Full Text PDF

Fluorescence imaging opens a new window for the diagnosis of early-stage Alzheimer's disease.

Biosens Bioelectron

December 2024

State Key Laboratory of Green Pesticide, International Joint Research Center for Intelligent Biosensor Technology and Health, Central China Normal University, Wuhan, 430079, PR China. Electronic address:

As the global population ages, the incidence and prevalence of Alzheimer's disease (AD) continues to rise, posing a serious threat to human health. Butyrylcholinesterase (BChE), which is overexpressed in the brains of patients with AD, is a potential drug target and biomarker. However, the molecular mechanism underlying BChE's role in the AD process remains unclear.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!