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Elucidation of Molecular Mechanism(s) of Cognition Enhancing Activity of Bacomind(®): A Standardized Extract of Bacopa Monnieri
BACKGROUND: Bacopa monnieri (L.) Wettst., commonly known as Brahmi, is renowned in Indian traditional system for its potent memory enhancing activity, which has been validated by various scientific studies. OBJECTIVE: The objective of this study was to understand the molecular mechanism of memory en...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5068128/ https://www.ncbi.nlm.nih.gov/pubmed/27761079 http://dx.doi.org/10.4103/0973-1296.191464 |
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author | Dethe, Shekhar Deepak, M Agarwal, Amit |
author_facet | Dethe, Shekhar Deepak, M Agarwal, Amit |
author_sort | Dethe, Shekhar |
collection | PubMed |
description | BACKGROUND: Bacopa monnieri (L.) Wettst., commonly known as Brahmi, is renowned in Indian traditional system for its potent memory enhancing activity, which has been validated by various scientific studies. OBJECTIVE: The objective of this study was to understand the molecular mechanism of memory enhancing activity of BacoMind(®) (BM), a standardized extract of B. monnieri. MATERIALS AND METHODS: BM was screened in vitro in a panel of cell-free and receptor-transfected cell assays. The purified enzymes/membrane homogenates/cells were incubated with substrate/standard ligand in the absence or presence of the test compound. The IC(50) values and EC(50) values were determined by nonlinear regression analysis of the concentration–response curves generated with mean replicate values using Hill equation curve fitting. RESULTS: BM was found to inhibit three enzymes; Catechol-O-methyl transferase (COMT), Prolyl endopeptidase (PEP), and Poly (ADP-ribose) polymerase (PARP). It also had an antagonistic effect on serotonin 6 and 2A (5-HT(6) and 5-HT(2A)) receptors(,) known to influence the different neurological pathways, associated with memory and learning disorders, age-associated memory impairment. CONCLUSION: BM was found to inhibit three enzymes namely, Catechol-O-methyl transferase (COMT), Prolyl endopeptidase (PEP), and Poly (ADP-ribose) polymerase (PARP). It also exhibited an antagonistic effect on 5-HT(6) and 5-HT(2A) receptors. SUMMARY: This study was conducted to understand the molecular mechanism of memory enhancing activity of a standardized extract of B. monnieri by was screening it in vitro in a panel of cell-free and receptor-transfected cell assays. The purified enzymes/membrane homogenates/cells were incubated with substrate/standard ligand in the absence or presence of the test compound. BM was found to inhibit three enzymes; Catechol-O-methyl transferase (COMT), Prolyl endopeptidase (PEP), and Poly (ADP-ribose) polymerase (PARP). It also had an antagonistic effect on serotonin(6) and(2A) (5-HT(6) and 5-HT(2A)) receptors, known to influence the different neurological pathways, associated with memory and learning disorders, age-associated memory impairment. Abbreviations used: HTRF: Homogenous time resolved fluorescence, cAMP: Cyclic adenosine monophosphate, CHO: Chinese hamster ovary, RFU: Relative fluorescence unit, pNP: Para nitro phenol, AMC: 7-amino-4-methylcoumarin, ELISA: Enzyme linked immunosorbent assay, Z-Pro-Pro-CHO: Z-prolyl-prolinal, HEK: Human embryonic kidney, TE: Trolox equivalent. |
format | Online Article Text |
id | pubmed-5068128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-50681282016-10-19 Elucidation of Molecular Mechanism(s) of Cognition Enhancing Activity of Bacomind(®): A Standardized Extract of Bacopa Monnieri Dethe, Shekhar Deepak, M Agarwal, Amit Pharmacogn Mag Original Article BACKGROUND: Bacopa monnieri (L.) Wettst., commonly known as Brahmi, is renowned in Indian traditional system for its potent memory enhancing activity, which has been validated by various scientific studies. OBJECTIVE: The objective of this study was to understand the molecular mechanism of memory enhancing activity of BacoMind(®) (BM), a standardized extract of B. monnieri. MATERIALS AND METHODS: BM was screened in vitro in a panel of cell-free and receptor-transfected cell assays. The purified enzymes/membrane homogenates/cells were incubated with substrate/standard ligand in the absence or presence of the test compound. The IC(50) values and EC(50) values were determined by nonlinear regression analysis of the concentration–response curves generated with mean replicate values using Hill equation curve fitting. RESULTS: BM was found to inhibit three enzymes; Catechol-O-methyl transferase (COMT), Prolyl endopeptidase (PEP), and Poly (ADP-ribose) polymerase (PARP). It also had an antagonistic effect on serotonin 6 and 2A (5-HT(6) and 5-HT(2A)) receptors(,) known to influence the different neurological pathways, associated with memory and learning disorders, age-associated memory impairment. CONCLUSION: BM was found to inhibit three enzymes namely, Catechol-O-methyl transferase (COMT), Prolyl endopeptidase (PEP), and Poly (ADP-ribose) polymerase (PARP). It also exhibited an antagonistic effect on 5-HT(6) and 5-HT(2A) receptors. SUMMARY: This study was conducted to understand the molecular mechanism of memory enhancing activity of a standardized extract of B. monnieri by was screening it in vitro in a panel of cell-free and receptor-transfected cell assays. The purified enzymes/membrane homogenates/cells were incubated with substrate/standard ligand in the absence or presence of the test compound. BM was found to inhibit three enzymes; Catechol-O-methyl transferase (COMT), Prolyl endopeptidase (PEP), and Poly (ADP-ribose) polymerase (PARP). It also had an antagonistic effect on serotonin(6) and(2A) (5-HT(6) and 5-HT(2A)) receptors, known to influence the different neurological pathways, associated with memory and learning disorders, age-associated memory impairment. Abbreviations used: HTRF: Homogenous time resolved fluorescence, cAMP: Cyclic adenosine monophosphate, CHO: Chinese hamster ovary, RFU: Relative fluorescence unit, pNP: Para nitro phenol, AMC: 7-amino-4-methylcoumarin, ELISA: Enzyme linked immunosorbent assay, Z-Pro-Pro-CHO: Z-prolyl-prolinal, HEK: Human embryonic kidney, TE: Trolox equivalent. Medknow Publications & Media Pvt Ltd 2016-07 /pmc/articles/PMC5068128/ /pubmed/27761079 http://dx.doi.org/10.4103/0973-1296.191464 Text en Copyright: © Pharmacognosy Magazine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Dethe, Shekhar Deepak, M Agarwal, Amit Elucidation of Molecular Mechanism(s) of Cognition Enhancing Activity of Bacomind(®): A Standardized Extract of Bacopa Monnieri |
title | Elucidation of Molecular Mechanism(s) of Cognition Enhancing Activity of Bacomind(®): A Standardized Extract of Bacopa Monnieri |
title_full | Elucidation of Molecular Mechanism(s) of Cognition Enhancing Activity of Bacomind(®): A Standardized Extract of Bacopa Monnieri |
title_fullStr | Elucidation of Molecular Mechanism(s) of Cognition Enhancing Activity of Bacomind(®): A Standardized Extract of Bacopa Monnieri |
title_full_unstemmed | Elucidation of Molecular Mechanism(s) of Cognition Enhancing Activity of Bacomind(®): A Standardized Extract of Bacopa Monnieri |
title_short | Elucidation of Molecular Mechanism(s) of Cognition Enhancing Activity of Bacomind(®): A Standardized Extract of Bacopa Monnieri |
title_sort | elucidation of molecular mechanism(s) of cognition enhancing activity of bacomind(®): a standardized extract of bacopa monnieri |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5068128/ https://www.ncbi.nlm.nih.gov/pubmed/27761079 http://dx.doi.org/10.4103/0973-1296.191464 |
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