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Effect of aqueous extracts of Achyranthes aspera Linn. on experimental animal model for inflammation
BACKGROUND: Achyranthes aspera is known as Chirchita (Hindi), Apamarga (Sanskrit), Aghedi (Gujarati), Apang (Bengali), Nayurivi (Tamil), Kalalat (Malyalam) and Agadha (Marathi) in our country. It possesses valuable medicinal properties and used in treatment of cough, bronchitis and rheumatism, malar...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644760/ https://www.ncbi.nlm.nih.gov/pubmed/23661870 http://dx.doi.org/10.4103/0257-7941.107362 |
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author | Bhosale, Uma A. Yegnanarayan, Radha Pophale, Prachi Somani, Rahul |
author_facet | Bhosale, Uma A. Yegnanarayan, Radha Pophale, Prachi Somani, Rahul |
author_sort | Bhosale, Uma A. |
collection | PubMed |
description | BACKGROUND: Achyranthes aspera is known as Chirchita (Hindi), Apamarga (Sanskrit), Aghedi (Gujarati), Apang (Bengali), Nayurivi (Tamil), Kalalat (Malyalam) and Agadha (Marathi) in our country. It possesses valuable medicinal properties and used in treatment of cough, bronchitis and rheumatism, malarial fever, dysentery, asthma, hypertension and diabetes in Indian folklore. Present study was designed to evaluate anti-inflammatory activity of an aqueous extracts of Achyranthes aspera (AEAA). MATERIALS AND METHODS: AEAA leaves and whole plant (i.e. Aqueous extracts of Achyranthes aspera leaves (AEAAL)/Aqueous extracts of A. aspera whole plant (AEAAW) were studied in albino mice using carrageenan induced left hind paw edema. Both extracts were subjected to preliminary phytochemical analysis and acute toxicity of the extracts was also studied using Organization for Economic Co-operation and Development OECD guidelines 423. RESULTS: Acute toxicity study confirmed toxic dose of AEAA to be more than 2,000 mg/kg. Flavonoids, alkaloids, saponins and triterpenoids were the major constituents found in extracts. AEAA reduced the edema induced by carrageenan by 35.71-54.76% on intraperitoneally administration of 400 mg/kg and 800 mg/kg as compared to the untreated control group. Diclofenac sodium at 10 mg/kg inhibited the edema volume by 42.85%. The results indicated that the AEAA 800 mg/kg body weight shows more significant (P < 0.01, P < 0.001) anti-inflammatory activity when compared with the standard and untreated control respectively. CONCLUSION: Both AEAA exhibit promising anti-inflammatory activity attributed to flavonoids, alkaloids, saponins and triterpenoids phytoconstituents. |
format | Online Article Text |
id | pubmed-3644760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36447602013-05-09 Effect of aqueous extracts of Achyranthes aspera Linn. on experimental animal model for inflammation Bhosale, Uma A. Yegnanarayan, Radha Pophale, Prachi Somani, Rahul Anc Sci Life Original Article BACKGROUND: Achyranthes aspera is known as Chirchita (Hindi), Apamarga (Sanskrit), Aghedi (Gujarati), Apang (Bengali), Nayurivi (Tamil), Kalalat (Malyalam) and Agadha (Marathi) in our country. It possesses valuable medicinal properties and used in treatment of cough, bronchitis and rheumatism, malarial fever, dysentery, asthma, hypertension and diabetes in Indian folklore. Present study was designed to evaluate anti-inflammatory activity of an aqueous extracts of Achyranthes aspera (AEAA). MATERIALS AND METHODS: AEAA leaves and whole plant (i.e. Aqueous extracts of Achyranthes aspera leaves (AEAAL)/Aqueous extracts of A. aspera whole plant (AEAAW) were studied in albino mice using carrageenan induced left hind paw edema. Both extracts were subjected to preliminary phytochemical analysis and acute toxicity of the extracts was also studied using Organization for Economic Co-operation and Development OECD guidelines 423. RESULTS: Acute toxicity study confirmed toxic dose of AEAA to be more than 2,000 mg/kg. Flavonoids, alkaloids, saponins and triterpenoids were the major constituents found in extracts. AEAA reduced the edema induced by carrageenan by 35.71-54.76% on intraperitoneally administration of 400 mg/kg and 800 mg/kg as compared to the untreated control group. Diclofenac sodium at 10 mg/kg inhibited the edema volume by 42.85%. The results indicated that the AEAA 800 mg/kg body weight shows more significant (P < 0.01, P < 0.001) anti-inflammatory activity when compared with the standard and untreated control respectively. CONCLUSION: Both AEAA exhibit promising anti-inflammatory activity attributed to flavonoids, alkaloids, saponins and triterpenoids phytoconstituents. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3644760/ /pubmed/23661870 http://dx.doi.org/10.4103/0257-7941.107362 Text en Copyright: © Ancient Science of Life 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Bhosale, Uma A. Yegnanarayan, Radha Pophale, Prachi Somani, Rahul Effect of aqueous extracts of Achyranthes aspera Linn. on experimental animal model for inflammation |
title | Effect of aqueous extracts of Achyranthes aspera Linn. on experimental animal model for inflammation |
title_full | Effect of aqueous extracts of Achyranthes aspera Linn. on experimental animal model for inflammation |
title_fullStr | Effect of aqueous extracts of Achyranthes aspera Linn. on experimental animal model for inflammation |
title_full_unstemmed | Effect of aqueous extracts of Achyranthes aspera Linn. on experimental animal model for inflammation |
title_short | Effect of aqueous extracts of Achyranthes aspera Linn. on experimental animal model for inflammation |
title_sort | effect of aqueous extracts of achyranthes aspera linn. on experimental animal model for inflammation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644760/ https://www.ncbi.nlm.nih.gov/pubmed/23661870 http://dx.doi.org/10.4103/0257-7941.107362 |
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