Publications des scientifiques de l'IRD

Bouquet J., Rivaud M., Chevalley Séverine, Deharo Eric, Jullian Valérie, Valentin A. (2012). Biological activities of nitidine, a potential antimalarial lead compound. Malaria Journal, 11, p. 67. ISSN 1475-2875.

Titre du document
Biological activities of nitidine, a potential antimalarial lead compound
Année de publication
2012
Type de document
Article référencé dans le Web of Science WOS:000302804700002
Auteurs
Bouquet J., Rivaud M., Chevalley Séverine, Deharo Eric, Jullian Valérie, Valentin A.
Source
Malaria Journal, 2012, 11, p. 67 ISSN 1475-2875
Background: Nitidine is thought to be the main active ingredient in several traditional anti-malarial remedies used in different parts of the world. The widespread use of these therapies stresses the importance of studying this molecule in the context of malaria control. However, little is known about its potential as an anti-plasmodial drug, as well as its mechanism of action. Methods: In this study, the anti-malarial potential of nitidine was evaluated in vitro on CQ-sensitive and -resistant strains. The nitidine's selectivity index compared with cancerous and non-cancerous cell lines was then determined. In vivo assays were then performed, using the four-day Peter's test methodology. To gain information about nitidine's possible mode of action, its moment of action on the parasite cell cycle was studied, and its localization inside the parasite was determined using confocal microscopy. The in vitro abilities of nitidine to bind haem and to inhibit beta-haematin formation were also demonstrated. Results: Nitidine showed similar in vitro activity in CQ-sensitive and resistant strains, and also a satisfying selectivity index (> 10) when compared with a non-cancerous cells line. Its in vivo activity was moderate; however, no sign of acute toxicity was observed during treatment. Nitidine's moment of action on the parasite cycle showed that it could not interfere with DNA replication; this was consistent with the observation that nitidine did not localize in the nucleus, but rather in the cytoplasm of the parasite. Nitidine was able to form a 1-1 complex with haem in vitro and also inhibited beta-haematin formation with the same potency as chloroquine. Conclusion: Nitidine can be considered a potential anti-malarial lead compound. Its ability to complex haem and inhibit beta-haematin formation suggests a mechanism of action similar to that of chloroquine. The anti-malarial activity of nitidine could therefore be improved by structural modification of this molecule to increase its penetration of the digestive vacuole in the parasite, where haemoglobin metabolization takes place.
Plan de classement
Entomologie médicale / Parasitologie / Virologie [052] ; Sciences du monde végétal [076]
Localisation
Fonds IRD [F B010055802]
Identifiant IRD
fdi:010055802
Contact