Planta Med 2007; 73(10): 1081-1088
DOI: 10.1055/s-2007-981579
Pharmacology
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

In Vitro Activity of 10-Deacetylbaccatin III against Leishmania donovani Promastigotes and Intracellular Amastigotes

Katerina Georgopoulou1 , 2 , Despina Smirlis1 , Sylvia Bisti1 , Evangelia Xingi1 , Leandros Skaltsounis2 , Ketty Soteriadou1
  • 1Laboratory of Molecular Parasitology, Department of Microbiology, Hellenic Pasteur Institute, Athens, Greece
  • 2Laboratory of Pharmacognosy and Pharmaceutical Chemistry, Department of Pharmacy, University of Athens, Athens, Greece
Further Information

Publication History

Received: February 15, 2007 Revised: June 27, 2007

Accepted: July 2, 2007

Publication Date:
09 August 2007 (online)

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Abstract

Current treatments for leishmaniasis are unsatisfactory due to their route of administration, toxicity and expense but, most importantly, to the developed resistance of Leishmania to first-line drugs. Therefore, the identification of new effective targeted drugs is an urgent need. Since many studies have shown that medicinal plants contain compounds active against protozoa we have undertaken a study aiming to determine the antileishmanial activity of the taxoid 10-deacetylbaccatin III, isolated from dried needles and small branches of the European yew tree (Taxus baccata). Interestingly, 10-deacetylbaccatin III was found to selectively inhibit the growth of L. donovani intracellular amastigotes within J774 murine macrophages in vitro at nanomolar concentrations with an IC50 value of 70 nM. Concentrations of 10-deacetylbaccatin III as high as 5 μM did not affect J774 murine macrophages whereas 20 nM of taxol, used as a control, was toxic to macrophages. The compound also inhibited the growth of L. donovani promastigotes but at higher concentrations with a maximum level of inhibition of 35 %. Taxol inhibited promastigote growth at micromolar concentrations. Comparison of the effect of 10-deacetylbaccatin III to that of taxol on cell cycle progression and cellular morphology showed that their mechanisms of action are different. The 10-deacetylbaccatin III-treated promastigotes were slightly arrested in the G2/M phase whereas taxol-treated cells were blocked in the G2/M phase. In addition 10-deacetylbaccatin III treatment, contrary to taxol, did not affect cellular morphology.

Abbreviations

cpm: counts per minute

FITC: fluorescein isothiocyanate

h: hour

OD: optical density

PBS: phosphate buffered saline

SDS: sodium dodecyl sulphate

References

Dr. Ketty Soteriadou

Laboratory of Molecular Parasitology

Department of Microbiology

Hellenic Pasteur Institute

127 Bas. Sofias Avenue

115 21 Athens

Greece

Phone: +30-210-6478-841

Fax: +30-210-6423-498

Email: ksoteriadou@pasteur.gr