*Corresponding Author:
A. Eltayeb
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Khartoum, P.O. Box 1996, Sudan
E-mail: [email protected]
Date of Submission 18 May 2011
Date of Revision 16 March 2012
Date of Acceptance 23 March 2012
Indian J Pharm Sci, 2012, 74 (2): 171-174  

 

Abstract

The antileishmanial activity of three organic solvent extracts and water residue of the plants: Acacia nilotica (Mimosaceae) (husk), Ambrosia miratima (Astraceae) (aerial shoot) and Azadarichta indica (Meliaceae) (leaves) were tested in vitro against Leishmania donovani promastigotes. The study revealed that the extracts of A. nilotica and A. miratima have effectious antileishmanial activity at concentrations (IC50) less than 8 µg/ml, while the extracts of A. indica lack antileishmanial activity. The chromatographic analysis of the ethyl acetate extract of A. nilotica, the most potent extract, resulted in four TLC fractions. Three of these fractions possessed antileishmanial activity. Phytochemical study of the potent fractions revealed the presence of poly hydroxyl compounds.

Keywords

Acacia nilotica, Ambrosia miratima, antileishmanial activity, Azadarichta indica

Leishmaniasis is an infection due to protozoa belonging to the genus Leishmania. Leishmaniasis is considered as a major public health problem in developing countries such as Sudan [1,2]. In Sudan where the primary health care is not always affordable, the use of herbal medicine is a common practice. However, very few studies were carried out to investigate the potential use of these medicinal plants in treatment of parasitic diseases [3,4].

The plant materials were collected according to their traditional use in folk medicine and a voucher specimen was kept in the Department of Pharmacognosy, Faculty of Pharmacy, University of Khartoum. The aqueous solution of the dried methanol extracts of the test plants were partitioned by liquid?liquid partitioning using petroleum ether, dichloromethane and ethyl acetate. The three organic solvent fractions and water residue were dried and dissolved in RPMI?1640 medium to prepare test concentrations of 0.5, 5, 25, 50 and 100 µg/ml.

Promastigotes of the identified strain of Leishmania donovani archidadi Mon 82 were grown in RPMI?1640 medium enriched with 20% foetal calf serum. Two hundred microlitre of each test extract (concentration 0.5?100 µg/ml) was added to 96 well plate (Nunc microtitre plate). To one raw, 200 µl of plane RPMI?1640 medium was added and this was kept as control. Then 50 µl of promastigotes suspension (3×106/ml) was added to all wells. Parasites were allowed to multiply at 24º for 24 h. Then promastigotes were harvested in a counting slide and counted under light microscope in comparison with control cells.

The ethyl acetate extract of A. nilotica (husk) was fractionated by TLC on silica gel (GF) plates using a solvent system of acetone and petroleum ether (1:1). The isolated TLC fractions were detected for their purity using Knauer HPLC machine in a Hypersil column (reversed phase C18) 5 µm, 15×4.6 mm. Mobile phase consisted of water and acetonitrile (30:70); flow rate was 1 ml/min and detection was on UV detector at 271 nm.

The UV spectrum of the aqueous solution (20%) of the TLC fractions having potent antileishmanial activity was measured at 120 nm/min scan speed on Perkin Elmer Lamda 2 UV/Vis spectrophotometer. FTIR machine (Shimadzu?800) was used to study the FTIR spectrum of KBr discs of dried crystals of the three above fractions.

Human peripheral blood mononuclear cells from heparinized blood were isolated using lymphoprep solution (Pharmacia Biotech). Each cell of 96 well round bottomed microtitre plate received 0.3×106/ml peripheral blood mononuclear cell (PBMC) in 200 µl of RPMI 1640 containing the plants extracts, concentration of 0.5, 5, 25, 50 and 100 µg/ml; 10 µl of phyto?haemaggulitinin (PHA, 47 µg/ml, Murex diagnostic, England) was added into all microplate wells except blank control ones, the positive control ones receive PHA but no plant extract was added to those wells.

The results of the present study reveal that, the extracts of A. nilotica husk and A. miratima aerial shoot have a potent antileishmanial activity in vitro against L. donovani promastigotes at concentrations (IC50 ) less than 8 µg/ml (Table 1). On the other hand the extracts of <em>A. indica</em> leaves did not give significant antileishmanial activity. As shown in Table 2 the thin layer chromatography of the ethyl acetate extract of A. nilotica husk indicated the presence of three fractions 1, 2 and 3 of Rf values: 0.70, 0.41 and 0.24, these fractions possessed potent antileishmanial activity with IC50 concentration less than 5 µg/ml. Where as the fourth fraction Rf value 0.00 (at base line) exhibited poor antileishmanial activity IC50 concentration more than 20 µg/ml. The performance of the different sensitivity and toxicity tests in this study were analyzed using SPSS computer software using the standard agent (pentostam) which exhibit relatively high IC50 of 156 µg/ml.

Plant extract solvent Y=a+bx IC50(µg/ml) IC90(µg/ml) R2
Acacia nilotica/Ethyl acetate Y=-2.13+2.413x 7.65 62.28 0.924
Acacia nilotica/Dichloromethane Y=-0.69+1.03x 4.6 624.0 0.625
Ambrosia maritima/Ethyl acetate Y=-0.45+0.761x 4.01 325.0 0.590
Ambrosia maritime/Dichloromethane Y=-1.1+1.65x 4.65 100.0 0.999
Ambrosia maritime/Petroleum ether Y=-1.43+2.63x 3.49 23.9 0.687
Ambrosia maritima/Water residual Y=-0.45+0.98x 2.9 520.0 0.188
Azadarichtaindica/Ethyl acetate Y=-4.05+0.90x 31900.0 8857169 0.835
Azadarichtaindica/Dichloromethane Y=-2.84+0.68x 14865.0 >25432544 0.410
Azadarichtaindica/Petroleum ether Y=-3.36+0.81x 14095.0 >7323899 1.000
Azadarichtaindica/Water residual Y=-3.34+0.93x 3818.9 >871619 0.939

Table 1: The Antileishmanial Effect Of The Medicinal Plants Extracts.

TLC Fractions of A. nilotica ethyl acetate extract Y=a+bx IC50(µg/ml) IC90(µg/ml) R2
Fraction (1) Rf=0.70 Y=-1.39+2.04x 4.80 57.80 0.496
Fraction (2) Rf=0.41 Y=-0.819+1.83x 2.80 44.80 0.832
Fraction (3) Rf=0.24 Y=-0.3+1.46x 1.60 51.66 0.966
Fraction (4) Rf=0.00 Y=-1.497+1.46x 22.39 712.20 0.525

Table 2: The Antileishmanial Activity Of Tlc Fractions (1-4) Of Acacia Nilotica Dried Ethylacetate Extract.

Fraction 1 Fraction 2 Fraction 3 Putativechemicalgroup Absorptionband(cm-1)
+ + + O-H 3500-3200
+ + + C-H(aliphatic 2950
      origin)  
+ - + –C=O 1750-1650
+ + + –C=C– 1650-1600
+ + + –CH3 and 1450-1400
      –CH2-  
+ + + C-O Multiple
      (different bands
      environments) 1300-1000
+ - - C-Cl 600

Table 3: Ir Analysis Results Of Tlc Fractions Of The Ethyl Acetate Extract Of Acacia Nilotica Husk.

The HPLC chromatogram of fraction 1 showed a single principle peak at Rt of 3.28 min with minor impurities, while chromatograms of fraction 2 and 3 show multiple peaks. The spectroscopic analysis of the TLC fractions of the ethyl acetate extract of A. nilotica husk provided the following results: The UV spectrum of aqueous solutions of fraction 1 showed absorption bands at 278.6, 262.3 and strong end absorption at 228.3 nm. With fraction 2 the UV spectrum revealed strong end absorption at 210 nm and shoulders at 423.2, 378 and 276 nm. The UV spectrum of fraction 3 gave strong end absorption with a single shoulder at 277.7 nm in aqueous solution. The IR spectrum absorption bands of TLC fractions of the ethyl acetate extract of Acacia nilotica husk are listed in Table 3.

The present work aimed at screening the antileishmanial activity of some Sudanese medicinal plants by in vitro studies to identify their active extracts or principles. The ethyl acetate extract of A. nilotica husk showed a promising antileishmanial activity. The findings of the present study agree with the earlier reports where, the ethyl acetate extract of A. nilotica husk had showed potent antiparasitic activity against Plasmodium falciprum. A. nilotica is widely used in folk medicine to treat a variety of diseases, where the gum stem bark, leaves and fruits are used for treatment of colds, bronchitis, pneumonia, ophthalmia, diarrhea and hemorrhage [5]. In a preliminary phytochemical screening of the ethyl acetate extract of A. nilotica husk, the presence of tannins and phenolic compounds was confirmed when a blue?black color was observed when ferric chloride reagent was added to a solution of the extract.

Several studies stated that many plant species have immunomodulatory action [6]. The ethyl acetate extract of A. nilotica husk, at low concentrations revealed an increase of human lymphocytes cells count. This may be an indication of the ability of this extract to enhance human immunity. TLC fractioning of the ethyl acetate extract of A. nilotica husk using silica gel GF as stationary phase and a solvent system of acetone: petroleum ether (1:1) was carried out. Four fractions were isolated of Rf values of 0.70, 0.41, 0.24 and baseline spot. The first three fractions were found to posses antileishmanial activity with IC50 value of 4.8, 2.8, 1.6 μg/ml and IC90 value of 57.8, 44.8 and 51.66 μg/ml, respectively. The isolated TLC fractions were detected for their purity using Knauer HPLC machine. Fraction 1 was found to be the most pure, while fraction 2 and 3 showed multiple peaks as an indication of the presence of other compounds in each fraction. The high antileishmanial activity of fraction 2 and 3 may be attributed to synergistic action of these additional compounds.

A potent antileishmanial activity was observed when L. donovani was treated with A. maritima extracts (IC50 <5 µg/ml). Further in vivo studies are needed to confirm the bioactivity of this plant.

The present study concludes that A. indica leaves lack anti leishmanial activity (IC50 value >1 mg/ml). In a previous study, it was reported that the methanol extract of A. indica leaves exhibited a moderate antileishmanial activity [7]. In fact, A. indicapreparations are used locally in treatment of many parasitic diseases. Oil extracted from the seeds is used in both man and animals as an anthelmintic, and in scabies, abdominal ulcers, rheumatism and muscular pain [8].

The extracts of the tested plants illustrates the diversity of antiprotozoal compounds found in those plants. Some of them may act on systems present in the parasite which are absent in the host cells. These are worthy of further study and perhaps semi synthetic modification in order to improve their therapeutic/toxic ratios.

Acknowledgements

Authors acknowledge the help of Dr. Ibrahim M. A. Sudanese, Botanist, Department of Pharmacognosy, Faculty of Pharmacy, University of Khatoum for plant authentication.

References