Erdener BALIKÇI
(Kocaeli Üniversitesi, Tıp Fakültesi, Mikrobiyoloji Anabilim Dalı, Kocaeli, TÜRKİYE)
Nurdan GÜNGÖR
(Kocaeli Üniversitesi, Tıp Fakültesi, Mikrobiyoloji Anabilim Dalı, Kocaeli, TÜRKİYE)
Fetiye KOLAYLI
(Kocaeli Üniversitesi, Tıp Fakültesi, Mikrobiyoloji Anabilim Dalı, Kocaeli, TÜRKİYE)
Murat HÖKELEK
(Kocaeli Üniversitesi, Tıp Fakültesi, Mikrobiyoloji Anabilim Dalı, Kocaeli, TÜRKİYE)
Yıl: 2021Cilt: 27Sayı: 1ISSN: 1300-6045 / 1309-2251Sayfa Aralığı: 51 - 56İngilizce

60 0
In Vitro Eff ect of Pelargonium sidoides on Promastigote Forms of Leishmania infantum and Leishmania tropica
Leishmaniasis is recognized as a neglected disease by the World Health Organization (WHO). New treatment modalities are needed for the treatment of leishmaniasis due to the limited number of drugs that can cause toxic side eff ects. Therefore, studies are being carried out on herbal extracts, which can be potential candidates for the treatment. Pelargonium sidoides a perennial herb originating in Africa, is used to treat infectious diseases. The aim of this study was to perform in vitro investigation of the direct eff ect of P. sidoides commercially available root extract (EPs 7630) on promastigotes of Leishmania infantum and Leishmania tropica. For this purpose, L. infantum and L. tropica strains were grown on NNN medium and then transferred into RPMI 1640 medium supported by 10% fetal bovine serum. After mass growing, the promastigotes were placed into 96-well plates with L. infantum as 5x104 and L. tropica as 1.5x105 . EPs 7630 was diluted at a concentration of 400, 200, 100 and 50 µg/mL. Afterwards, EPs 7630 was added and then counted by hemocytometry at 24, 48, 72, and 96 h. The calculations were done after the experiments repeated three times. Comparison with the control group and liposomal amphotericin B showed that EPs 7630 had no inhibitory eff ect on the growth of Leishmania promastigotes at the concentrations of 50 and 100 µg/mL, a partial inhibitory eff ect at 200 µg/mL, and an inhibitory eff ect at 400 µg/mL. It was concluded that identifying the substance(s) responsible for the antileishmanial eff ect of P. sidoides extract, conducting toxicity studies, and improving the results of these studies in in vivo models may be useful as steps for future clinical studies.
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