Original ArticlePharmacognosy MagazineVol. 11 | Issue 42s | 2015 | pp. 29–36Open access
S29 Antimutagenic potential of harpagoside and Harpagophytum procumbens against 1‑nitropyrene
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- 1 Botta Alain Department of Biogenotoxicology, Human Health and Environment, Mediterranean Institute of Biodiversity and Ecology, Faculty of Medicine, Aix‑Marseille University, 27 Bd Jean Moulin, France.
- 2 Laboratory of Pharmacognosy and Ethnopharmacology, Faculty of Pharmacy, Aix‑Marseille University, 27 Bd Jean Moulin, Marseille Cedex 5, France.
Published in Pharmacognosy Magazine
Correspondence: Luigi Manon
Botta Alain Department of Biogenotoxicology, Human Health and Environment, Mediterranean Institute of Biodiversity and Ecology, Faculty of Medicine, Aix‑Marseille University, 27 Bd Jean Moulin, France.
Email: manon.luigi@univ‑amu.fr
Copyright: © 2015 Manuscript Technomedia. This is an open access article.
- Published:
- May 27, 2015
- Received:
- Jul 18, 2014
How to cite
Manon, L., Béatrice, B., Thierry, O., Jocelyne, P., Fathi, M., & Evelyne, O. (2015). S29 Antimutagenic potential of harpagoside and Harpagophytum procumbens against 1‑nitropyrene. Pharmacognosy Magazine, 11(42s), 29–36. https://doi.org/10.4103/0973-1296.157675
Abstract
Background: 1‑nitropyrene (1‑NPy) is one of the most abundant nitro‑polycyclic aromatic hydrocarbons particularly in diesel exhausts. It is a mutagenic and carcinogenic pollutant very widespread in the environment. So the discovery of antimutagenic agents is essential. Harpagophytum procumbens (HP) is traditionally used as anti‑inflammatory and analgesic particularly against painful osteoarthritis. Harpagoside (HS), its major iridoid glycoside, is considered as the main active component. Objective: The aim of the present study was to evaluate the antimutagenic activity of HS and HP extracts against mutagenic activity of 1‑NPy. Materials and Methods: The antimutagenic activity was investigated using the in vitro cytokinesis‑block micronucleus assay in cultured human lymphocytes. Cells were exposed to HS or HP extracts before (pretreatment), during (co‑treatment), and after (posttreatment) treatment with 1‑NPy. Results: Results showed that HS significantly reduced the mutagenicity of 1‑NPy in pretreatment and particularly in co‑treatment, whereas all HP extracts significantly reduced the genotoxicity in the three protocols. Conclusion: These results suggested that HS was strongly involved in antimutagenic activity of HP extracts in co‑treatment, but other components in HP extracts participated in this activity in pre‑ and post‑treatment.
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Article metadata
| Title | S29 Antimutagenic potential of harpagoside and Harpagophytum procumbens against 1‑nitropyrene |
|---|---|
| Authors | Luigi Manon; Baghdikian Béatrice; Orsière Thierry; Pompili Jocelyne; Mabrouki Fathi; Ollivier Evelyne |
| Affiliations | Botta Alain Department of Biogenotoxicology, Human Health and Environment, Mediterranean Institute of Biodiversity and Ecology, Faculty of Medicine, Aix‑Marseille University, 27 Bd Jean Moulin, France.; Laboratory of Pharmacognosy and Ethnopharmacology, Faculty of Pharmacy, Aix‑Marseille University, 27 Bd Jean Moulin, Marseille Cedex 5, France. |
| Corresponding author | manon.luigi@univ‑amu.fr |
| Journal | Pharmacognosy Magazine |
| Volume / Issue | Vol. 11, Issue 42s (2015) |
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