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Neuroprotective activity of novel phenanthrene derivative from Grewia tiliaefolia by in vitro and in silico studies
Medicinal plants possess range of phytochemicals accountable for their diverse biological activities. Presently, such compounds have been isolated from medicinal plants, characterized and evaluated for their pharmacological potential. In the present study, the efforts have been made to isolate the c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9918530/ https://www.ncbi.nlm.nih.gov/pubmed/36765125 http://dx.doi.org/10.1038/s41598-023-29446-7 |
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author | Rajput, Ankita Sharma, Palvi Kumar, Nitish Kaur, Sarabjit Arora, Saroj |
author_facet | Rajput, Ankita Sharma, Palvi Kumar, Nitish Kaur, Sarabjit Arora, Saroj |
author_sort | Rajput, Ankita |
collection | PubMed |
description | Medicinal plants possess range of phytochemicals accountable for their diverse biological activities. Presently, such compounds have been isolated from medicinal plants, characterized and evaluated for their pharmacological potential. In the present study, the efforts have been made to isolate the compound(s) from Grewia tiliaefolia Vahl., plant known for its ameliorative effect on brain related diseases such as anxiety, depression, cognitive disorders and Parkinson’s disease. Plant extract was subjected to isolation of compound(s) using column chromatography and isolated compound was characterized by NMR FTIR and LCMS. The isolated compound was novel with the IUPAC name of the compound is propyl 3-hydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene-17-carboxylate, designated as A-1 and has not been reported before. A-1 was further evaluated for its antioxidant potential using in vitro antioxidant assays (2,2-diphenyl-1-picryl-hydrazyl-hydrate, DPPH assay and reducing power assay, RPA). Also, Acetylcholinesterase (AChE) inhibitory potential of A-1 and extract was analysed. Results showed that A-1 exhibited significantly higher antioxidant activity in both DPPH and RPA assay as compared to plant extract. In case of AChE inhibitory activity again, A-1 has shown significantly higher activity as compared to plant extract. In silico study was conducted to predict its action on proteins playing crucial role in neurological and neurodegenerative disorders such as gamma amino butyric acid (GABA) receptor and glutamate α amino-3-hydroxyl-5-methyl-4-isoxazolepropionic acid (Glu AMPA) receptor in epilepsy and AChE enzyme in Alzheimer’s diseases. The compound has shown interaction in following order: AChE > GABA receptor > Glu AMPA receptor. Further, molecular dynamic simulations and ADME studies of A-1 and AChE enzyme revealed that A-1 yielded good results in all parameters and hence can relieve Alzheimer’s like symptoms. |
format | Online Article Text |
id | pubmed-9918530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99185302023-02-12 Neuroprotective activity of novel phenanthrene derivative from Grewia tiliaefolia by in vitro and in silico studies Rajput, Ankita Sharma, Palvi Kumar, Nitish Kaur, Sarabjit Arora, Saroj Sci Rep Article Medicinal plants possess range of phytochemicals accountable for their diverse biological activities. Presently, such compounds have been isolated from medicinal plants, characterized and evaluated for their pharmacological potential. In the present study, the efforts have been made to isolate the compound(s) from Grewia tiliaefolia Vahl., plant known for its ameliorative effect on brain related diseases such as anxiety, depression, cognitive disorders and Parkinson’s disease. Plant extract was subjected to isolation of compound(s) using column chromatography and isolated compound was characterized by NMR FTIR and LCMS. The isolated compound was novel with the IUPAC name of the compound is propyl 3-hydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene-17-carboxylate, designated as A-1 and has not been reported before. A-1 was further evaluated for its antioxidant potential using in vitro antioxidant assays (2,2-diphenyl-1-picryl-hydrazyl-hydrate, DPPH assay and reducing power assay, RPA). Also, Acetylcholinesterase (AChE) inhibitory potential of A-1 and extract was analysed. Results showed that A-1 exhibited significantly higher antioxidant activity in both DPPH and RPA assay as compared to plant extract. In case of AChE inhibitory activity again, A-1 has shown significantly higher activity as compared to plant extract. In silico study was conducted to predict its action on proteins playing crucial role in neurological and neurodegenerative disorders such as gamma amino butyric acid (GABA) receptor and glutamate α amino-3-hydroxyl-5-methyl-4-isoxazolepropionic acid (Glu AMPA) receptor in epilepsy and AChE enzyme in Alzheimer’s diseases. The compound has shown interaction in following order: AChE > GABA receptor > Glu AMPA receptor. Further, molecular dynamic simulations and ADME studies of A-1 and AChE enzyme revealed that A-1 yielded good results in all parameters and hence can relieve Alzheimer’s like symptoms. Nature Publishing Group UK 2023-02-10 /pmc/articles/PMC9918530/ /pubmed/36765125 http://dx.doi.org/10.1038/s41598-023-29446-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Rajput, Ankita Sharma, Palvi Kumar, Nitish Kaur, Sarabjit Arora, Saroj Neuroprotective activity of novel phenanthrene derivative from Grewia tiliaefolia by in vitro and in silico studies |
title | Neuroprotective activity of novel phenanthrene derivative from Grewia tiliaefolia by in vitro and in silico studies |
title_full | Neuroprotective activity of novel phenanthrene derivative from Grewia tiliaefolia by in vitro and in silico studies |
title_fullStr | Neuroprotective activity of novel phenanthrene derivative from Grewia tiliaefolia by in vitro and in silico studies |
title_full_unstemmed | Neuroprotective activity of novel phenanthrene derivative from Grewia tiliaefolia by in vitro and in silico studies |
title_short | Neuroprotective activity of novel phenanthrene derivative from Grewia tiliaefolia by in vitro and in silico studies |
title_sort | neuroprotective activity of novel phenanthrene derivative from grewia tiliaefolia by in vitro and in silico studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9918530/ https://www.ncbi.nlm.nih.gov/pubmed/36765125 http://dx.doi.org/10.1038/s41598-023-29446-7 |
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