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Elucidation of in-vitro anti-inflammatory bioactive compounds isolated from Jatropha curcas L. plant root
BACKGROUND: The Jatropha curcas plant or locally known as “Pokok Jarak” has been widely used in traditional medical applications. This plant is used to treat various conditions such as arthritis, gout, jaundice, wound and inflammation. However, the nature of compounds involved has not been well docu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330596/ https://www.ncbi.nlm.nih.gov/pubmed/25652309 http://dx.doi.org/10.1186/s12906-015-0528-4 |
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author | Othman, Ahmad Razi Abdullah, Norhani Ahmad, Syahida Ismail, Intan Safinar Zakaria, Mohamad Pauzi |
author_facet | Othman, Ahmad Razi Abdullah, Norhani Ahmad, Syahida Ismail, Intan Safinar Zakaria, Mohamad Pauzi |
author_sort | Othman, Ahmad Razi |
collection | PubMed |
description | BACKGROUND: The Jatropha curcas plant or locally known as “Pokok Jarak” has been widely used in traditional medical applications. This plant is used to treat various conditions such as arthritis, gout, jaundice, wound and inflammation. However, the nature of compounds involved has not been well documented. Hence, this study was conducted to investigate the anti-inflammatory activity of different parts of J. curcas plant and to identify the active compounds involved. METHODS: In this study, methanol (80%) extraction of four different parts (leaves, fruits, stem and root) of J. curcas plant was carried out. Phenolic content of each part was determined by using Folin-Ciocalteau reagent. Gallic acid was used as the phenol standard. Each plant part was screened for anti-inflammatory activity using cultured macrophage RAW 264.7 cells. The active plant part was then partitioned with hexane, chloroform, ethyl acetate and water. Each partition was again screened for anti-inflammatory activity. The active partition was then fractionated using an open column chromatography system. Single spots isolated from column chromatography were assayed for anti-inflammatory and cytotoxicity activities. Spots that showed activity were subjected to gas chromatography mass spectrophotometry (GC-MS) analysis for identification of active metabolites. RESULTS: The hexane partition from root extract showed the highest anti-inflammatory activity. However, it also showed high cytotoxicity towards RAW 264.7 cells at 1 mg/mL. Fractionation process using column chromatography showed five spots. Two spots labeled as H-4 and H-5 possessed anti-inflammatory activity, without cytotoxicity activity. Analysis of both spots by GC-MS showed the presence of hexadecanoic acid methyl ester, octadecanoic acid methyl ester and octadecanoic acid. CONCLUSION: This finding suggests that hexadecanoic acid methyl ester, octadecanoic acid methyl ester and octadecanoic acid could be responsible for the anti-inflammatory activity of the J. curcas root extract. |
format | Online Article Text |
id | pubmed-4330596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43305962015-02-18 Elucidation of in-vitro anti-inflammatory bioactive compounds isolated from Jatropha curcas L. plant root Othman, Ahmad Razi Abdullah, Norhani Ahmad, Syahida Ismail, Intan Safinar Zakaria, Mohamad Pauzi BMC Complement Altern Med Research Article BACKGROUND: The Jatropha curcas plant or locally known as “Pokok Jarak” has been widely used in traditional medical applications. This plant is used to treat various conditions such as arthritis, gout, jaundice, wound and inflammation. However, the nature of compounds involved has not been well documented. Hence, this study was conducted to investigate the anti-inflammatory activity of different parts of J. curcas plant and to identify the active compounds involved. METHODS: In this study, methanol (80%) extraction of four different parts (leaves, fruits, stem and root) of J. curcas plant was carried out. Phenolic content of each part was determined by using Folin-Ciocalteau reagent. Gallic acid was used as the phenol standard. Each plant part was screened for anti-inflammatory activity using cultured macrophage RAW 264.7 cells. The active plant part was then partitioned with hexane, chloroform, ethyl acetate and water. Each partition was again screened for anti-inflammatory activity. The active partition was then fractionated using an open column chromatography system. Single spots isolated from column chromatography were assayed for anti-inflammatory and cytotoxicity activities. Spots that showed activity were subjected to gas chromatography mass spectrophotometry (GC-MS) analysis for identification of active metabolites. RESULTS: The hexane partition from root extract showed the highest anti-inflammatory activity. However, it also showed high cytotoxicity towards RAW 264.7 cells at 1 mg/mL. Fractionation process using column chromatography showed five spots. Two spots labeled as H-4 and H-5 possessed anti-inflammatory activity, without cytotoxicity activity. Analysis of both spots by GC-MS showed the presence of hexadecanoic acid methyl ester, octadecanoic acid methyl ester and octadecanoic acid. CONCLUSION: This finding suggests that hexadecanoic acid methyl ester, octadecanoic acid methyl ester and octadecanoic acid could be responsible for the anti-inflammatory activity of the J. curcas root extract. BioMed Central 2015-02-05 /pmc/articles/PMC4330596/ /pubmed/25652309 http://dx.doi.org/10.1186/s12906-015-0528-4 Text en © Othman et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Othman, Ahmad Razi Abdullah, Norhani Ahmad, Syahida Ismail, Intan Safinar Zakaria, Mohamad Pauzi Elucidation of in-vitro anti-inflammatory bioactive compounds isolated from Jatropha curcas L. plant root |
title | Elucidation of in-vitro anti-inflammatory bioactive compounds isolated from Jatropha curcas L. plant root |
title_full | Elucidation of in-vitro anti-inflammatory bioactive compounds isolated from Jatropha curcas L. plant root |
title_fullStr | Elucidation of in-vitro anti-inflammatory bioactive compounds isolated from Jatropha curcas L. plant root |
title_full_unstemmed | Elucidation of in-vitro anti-inflammatory bioactive compounds isolated from Jatropha curcas L. plant root |
title_short | Elucidation of in-vitro anti-inflammatory bioactive compounds isolated from Jatropha curcas L. plant root |
title_sort | elucidation of in-vitro anti-inflammatory bioactive compounds isolated from jatropha curcas l. plant root |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330596/ https://www.ncbi.nlm.nih.gov/pubmed/25652309 http://dx.doi.org/10.1186/s12906-015-0528-4 |
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