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  2. Evaluation of in vitro antiprotozoal activity of Ajuga laxmannii and its secondary metabolites

Evaluation of in vitro antiprotozoal activity of Ajuga laxmannii and its secondary metabolites

  • Pharm Biol. 2016 Sep;54(9):1808-14. doi: 10.3109/13880209.2015.1129542.
Irem Atay 1 2 Hasan Kirmizibekmez 2 Marcel Kaiser 3 Galip Akaydin 4 Erdem Yesilada 2 Deniz Tasdemir 5 6
Affiliations

Affiliations

  • 1 a Department of Pharmacognosy , School of Pharmacy, İstanbul Medipol University , İstanbul , 34810 , Turkey ;
  • 2 b Department of Pharmacognosy, Faculty of Pharmacy , Yeditepe University , İstanbul , 34755 , Turkey ;
  • 3 c Department of Medical Parasitology and Infection Biology , Swiss Tropical and Public Health Institute , Basel , Switzerland ;
  • 4 d Department of Biology Education , Hacettepe University , Beytepe , Ankara , Turkey ;
  • 5 e Department of Pharmaceutical and Biological Chemistry , Centre for Pharmacognosy and Phytotherapy, School of Pharmacy, University of London , London , UK ;
  • 6 f GEOMAR Helmholtz Centre for Ocean Research Kiel, Research Unit Marine Natural Products Chemistry , Kiel , Germany.
Abstract

Context Some Ajuga L. (Lamiaceae) species are traditionally used for the treatment of malaria, as well as fever, which is a common symptom of many parasitic diseases. Objective In the continuation of our studies on the identification of antiprotozoal secondary metabolites of Turkish Lamiaceae species, we have investigated the aerial parts of Ajuga laxmannii. Materials and methods The aerial parts of A. laxmannii were extracted with MeOH. The H2O subextract was subjected to polyamide, C18-MPLC and SiO2 CCs to yield eight metabolites. The structures of the isolates were elucidated by NMR spectroscopy and MS analyses. The extract, subextracts as well as the isolates were tested for their in vitro antiprotozoal activities against Plasmodium falciparum, Trypanasoma brucei rhodesiense, T. cruzi and Leishmania donovani at concentrations of 90-0.123 μg/mL. Results Two iridoid glycosides harpagide (1) and 8-O-acetylharpagide (2), three o-coumaric acid derivatives cis-melilotoside (3), trans-melilotoside (4) and dihydromelilotoside (5), two phenylethanoid glycosides verbascoside (6) and galactosylmartynoside (7) and a flavone-C-glycoside, isoorientin (8) were isolated. Many compounds showed moderate to good antiparasitic activity, with isoorientin (8) displaying the most significant antimalarial potential (an IC50 value of 9.7 μg/mL). Discussion and conclusion This is the first report on the antiprotozoal evaluation of A. laxmannii extracts and isolates. Furthermore, isoorientin and dihydromelilotoside are being reported for the first time from the genus Ajuga.

Keywords

Antiprotozoal activity; Isoorientin; Lamiaceae; flavonoid; iridoid glycosides; plasmodium.

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