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Atherogenic effect of Arecoline: A computational study
There are over 600 million people worldwide covering Asian and Oceanic countries including India have the habit of chewing areca nut as masticator in different forms. Arecoline (C(8)H(13)NO(2)) has been reported as one of the abundant constituents of areca nut. A good number of scientific publicatio...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Biomedical Informatics
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314877/ https://www.ncbi.nlm.nih.gov/pubmed/22493525 http://dx.doi.org/10.6026/97320630008229 |
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author | Choudhury, Manabendra Dutta Chetia, Pankaj Choudhury, Karabi Dutta Talukdar, Anupam Das Datta-choudhari, Mohan |
author_facet | Choudhury, Manabendra Dutta Chetia, Pankaj Choudhury, Karabi Dutta Talukdar, Anupam Das Datta-choudhari, Mohan |
author_sort | Choudhury, Manabendra Dutta |
collection | PubMed |
description | There are over 600 million people worldwide covering Asian and Oceanic countries including India have the habit of chewing areca nut as masticator in different forms. Arecoline (C(8)H(13)NO(2)) has been reported as one of the abundant constituents of areca nut. A good number of scientific publications have made Arecoline responsible for oral cancer. Based on observation from clinical situation in North East India, one of the most betel quid chewing region of the country, we suspected a link between consumption of areca nut and Cerebro Vascular Disease like stroke. Therefore, we considered Low Density Lipoprotein (LDL) receptor as target and Arecoline as ligand and studied ligand –target interaction using computational tools. Also we considered High Density Lipoprotein (HDL) receptor as another target to see if Arecoline has any binding potential with it over and above LDL receptor. Docking result indicated that Arecoline and Cholesterol both, have affinity towards extracellular domain of Human LDL receptor but affinity of Arecoline is much higher (-12.3560.) than that of Cholesterol(-0.1810). Docking of Arecoline and 1, 2-Hexyl-1- cyclopentanone thiosemicarbazone (thiosemicarbazone) with Bovine HDL receptor showed that Arecoline also has the potential (Score, -6.2690Kcal/Mol) to block HDL receptor though its potential is less than that (score, -10.0509 Kcal/Mol) of control (thiosemicarbazone). We, therefore, suggest that by inhibiting endocytosis of LDL cholesterol because of blocking LDL receptor function and also by preventing LDL cholesterol uptake by liver from blood because of interference with HDL receptor, Arecoline may contribute to atherosclerosis. The study therefore, indicates a positive correlation between chewing of betel quid and Cerebro Vascular Disease. |
format | Online Article Text |
id | pubmed-3314877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Biomedical Informatics |
record_format | MEDLINE/PubMed |
spelling | pubmed-33148772012-04-10 Atherogenic effect of Arecoline: A computational study Choudhury, Manabendra Dutta Chetia, Pankaj Choudhury, Karabi Dutta Talukdar, Anupam Das Datta-choudhari, Mohan Bioinformation Hypothesis There are over 600 million people worldwide covering Asian and Oceanic countries including India have the habit of chewing areca nut as masticator in different forms. Arecoline (C(8)H(13)NO(2)) has been reported as one of the abundant constituents of areca nut. A good number of scientific publications have made Arecoline responsible for oral cancer. Based on observation from clinical situation in North East India, one of the most betel quid chewing region of the country, we suspected a link between consumption of areca nut and Cerebro Vascular Disease like stroke. Therefore, we considered Low Density Lipoprotein (LDL) receptor as target and Arecoline as ligand and studied ligand –target interaction using computational tools. Also we considered High Density Lipoprotein (HDL) receptor as another target to see if Arecoline has any binding potential with it over and above LDL receptor. Docking result indicated that Arecoline and Cholesterol both, have affinity towards extracellular domain of Human LDL receptor but affinity of Arecoline is much higher (-12.3560.) than that of Cholesterol(-0.1810). Docking of Arecoline and 1, 2-Hexyl-1- cyclopentanone thiosemicarbazone (thiosemicarbazone) with Bovine HDL receptor showed that Arecoline also has the potential (Score, -6.2690Kcal/Mol) to block HDL receptor though its potential is less than that (score, -10.0509 Kcal/Mol) of control (thiosemicarbazone). We, therefore, suggest that by inhibiting endocytosis of LDL cholesterol because of blocking LDL receptor function and also by preventing LDL cholesterol uptake by liver from blood because of interference with HDL receptor, Arecoline may contribute to atherosclerosis. The study therefore, indicates a positive correlation between chewing of betel quid and Cerebro Vascular Disease. Biomedical Informatics 2012-03-17 /pmc/articles/PMC3314877/ /pubmed/22493525 http://dx.doi.org/10.6026/97320630008229 Text en © 2012 Biomedical Informatics This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited. |
spellingShingle | Hypothesis Choudhury, Manabendra Dutta Chetia, Pankaj Choudhury, Karabi Dutta Talukdar, Anupam Das Datta-choudhari, Mohan Atherogenic effect of Arecoline: A computational study |
title | Atherogenic effect of Arecoline: A computational study |
title_full | Atherogenic effect of Arecoline: A computational study |
title_fullStr | Atherogenic effect of Arecoline: A computational study |
title_full_unstemmed | Atherogenic effect of Arecoline: A computational study |
title_short | Atherogenic effect of Arecoline: A computational study |
title_sort | atherogenic effect of arecoline: a computational study |
topic | Hypothesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314877/ https://www.ncbi.nlm.nih.gov/pubmed/22493525 http://dx.doi.org/10.6026/97320630008229 |
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