Kinetics and computational analysis of cholinesterase inhibition by REVERC3, a bisdemethoxycurcumin-rich extract: Relevance to the treatment of Alzheimer’s disease

Objectives: Cholinesterase inhibition is a common strategy to treat Alzheimer’s disease. In this study, we have investigated the cholinesterase inhibitory effects of a first-of-its-kind turmeric extract (REVERC3) having enriched content of bisdemethoxycurcumin as major active curcuminoid. Methods :...

Full description

Bibliographic Details
Main Authors: Sudeep HV, Amritha Raj, Gouthamchandra K, Chandrappa S, Shyamprasad K
Format: Article
Language:English
Published: SAGE Publishing 2020-11-01
Series:SAGE Open Medicine
Online Access:https://doi.org/10.1177/2050312120973499
id doaj-5e812b29858f461dbfe9d8c7e36e7e96
record_format Article
spelling doaj-5e812b29858f461dbfe9d8c7e36e7e962020-11-25T04:10:35ZengSAGE PublishingSAGE Open Medicine2050-31212020-11-01810.1177/2050312120973499Kinetics and computational analysis of cholinesterase inhibition by REVERC3, a bisdemethoxycurcumin-rich extract: Relevance to the treatment of Alzheimer’s diseaseSudeep HVAmritha RajGouthamchandra KChandrappa SShyamprasad KObjectives: Cholinesterase inhibition is a common strategy to treat Alzheimer’s disease. In this study, we have investigated the cholinesterase inhibitory effects of a first-of-its-kind turmeric extract (REVERC3) having enriched content of bisdemethoxycurcumin as major active curcuminoid. Methods : The inhibition studies were performed using Ellman’s colorimetric assay. The kinetics of acetylcholinesterase and butyrylcholinesterase was determined in the presence of REVERC3 using the Lineweaver–Burk double reciprocal plots. Furthermore, we used AutoDock tools to predict the binding of bisdemethoxycurcumin with the active sites of cholinesterases. Results : REVERC3 showed 4.8- and 5.39-fold higher inhibitory potential of acetylcholinesterase and butyrylcholinesterase with IC50 values of 29.08 and 33.59 µg/mL, respectively, compared to the regular turmeric extract. The mode of binding of REVERC3 was competitive in the case of acetylcholinesterase while it was uncompetitive for the inhibition of butyrylcholinesterase. Docking analysis revealed that bisdemethoxycurcumin, the major constituent of REVERC3, has different preferences of binding in the active sites of acetylcholinesterase and butyrylcholinesterase. However, the best binding pose predictions are in line with the experimental binding mode of the cholinesterases. Conclusion : These results indicate that bisdemethoxycurcumin-enriched turmeric extract could improve the cholinergic functions via dual inhibition of cholinesterases. However, the predominant role of bisdemethoxycurcumin in REVERC3 must be further validated using preclinical studies and clinical trials.https://doi.org/10.1177/2050312120973499
collection DOAJ
language English
format Article
sources DOAJ
author Sudeep HV
Amritha Raj
Gouthamchandra K
Chandrappa S
Shyamprasad K
spellingShingle Sudeep HV
Amritha Raj
Gouthamchandra K
Chandrappa S
Shyamprasad K
Kinetics and computational analysis of cholinesterase inhibition by REVERC3, a bisdemethoxycurcumin-rich extract: Relevance to the treatment of Alzheimer’s disease
SAGE Open Medicine
author_facet Sudeep HV
Amritha Raj
Gouthamchandra K
Chandrappa S
Shyamprasad K
author_sort Sudeep HV
title Kinetics and computational analysis of cholinesterase inhibition by REVERC3, a bisdemethoxycurcumin-rich extract: Relevance to the treatment of Alzheimer’s disease
title_short Kinetics and computational analysis of cholinesterase inhibition by REVERC3, a bisdemethoxycurcumin-rich extract: Relevance to the treatment of Alzheimer’s disease
title_full Kinetics and computational analysis of cholinesterase inhibition by REVERC3, a bisdemethoxycurcumin-rich extract: Relevance to the treatment of Alzheimer’s disease
title_fullStr Kinetics and computational analysis of cholinesterase inhibition by REVERC3, a bisdemethoxycurcumin-rich extract: Relevance to the treatment of Alzheimer’s disease
title_full_unstemmed Kinetics and computational analysis of cholinesterase inhibition by REVERC3, a bisdemethoxycurcumin-rich extract: Relevance to the treatment of Alzheimer’s disease
title_sort kinetics and computational analysis of cholinesterase inhibition by reverc3, a bisdemethoxycurcumin-rich extract: relevance to the treatment of alzheimer’s disease
publisher SAGE Publishing
series SAGE Open Medicine
issn 2050-3121
publishDate 2020-11-01
description Objectives: Cholinesterase inhibition is a common strategy to treat Alzheimer’s disease. In this study, we have investigated the cholinesterase inhibitory effects of a first-of-its-kind turmeric extract (REVERC3) having enriched content of bisdemethoxycurcumin as major active curcuminoid. Methods : The inhibition studies were performed using Ellman’s colorimetric assay. The kinetics of acetylcholinesterase and butyrylcholinesterase was determined in the presence of REVERC3 using the Lineweaver–Burk double reciprocal plots. Furthermore, we used AutoDock tools to predict the binding of bisdemethoxycurcumin with the active sites of cholinesterases. Results : REVERC3 showed 4.8- and 5.39-fold higher inhibitory potential of acetylcholinesterase and butyrylcholinesterase with IC50 values of 29.08 and 33.59 µg/mL, respectively, compared to the regular turmeric extract. The mode of binding of REVERC3 was competitive in the case of acetylcholinesterase while it was uncompetitive for the inhibition of butyrylcholinesterase. Docking analysis revealed that bisdemethoxycurcumin, the major constituent of REVERC3, has different preferences of binding in the active sites of acetylcholinesterase and butyrylcholinesterase. However, the best binding pose predictions are in line with the experimental binding mode of the cholinesterases. Conclusion : These results indicate that bisdemethoxycurcumin-enriched turmeric extract could improve the cholinergic functions via dual inhibition of cholinesterases. However, the predominant role of bisdemethoxycurcumin in REVERC3 must be further validated using preclinical studies and clinical trials.
url https://doi.org/10.1177/2050312120973499
work_keys_str_mv AT sudeephv kineticsandcomputationalanalysisofcholinesteraseinhibitionbyreverc3abisdemethoxycurcuminrichextractrelevancetothetreatmentofalzheimersdisease
AT amritharaj kineticsandcomputationalanalysisofcholinesteraseinhibitionbyreverc3abisdemethoxycurcuminrichextractrelevancetothetreatmentofalzheimersdisease
AT gouthamchandrak kineticsandcomputationalanalysisofcholinesteraseinhibitionbyreverc3abisdemethoxycurcuminrichextractrelevancetothetreatmentofalzheimersdisease
AT chandrappas kineticsandcomputationalanalysisofcholinesteraseinhibitionbyreverc3abisdemethoxycurcuminrichextractrelevancetothetreatmentofalzheimersdisease
AT shyamprasadk kineticsandcomputationalanalysisofcholinesteraseinhibitionbyreverc3abisdemethoxycurcuminrichextractrelevancetothetreatmentofalzheimersdisease
_version_ 1724420074636312576