Background
Despite the incessant global efforts to fight parasitic infections and the attempts to eliminate the causative organisms, malaria still remains as one of the greatest human killers, causing almost 1 million deaths per year (mainly small children in Africa) and 300-400 million infections annually [
1]. In the South East Asian Region of WHO, people living in eleven countries are exposed to the risk of malaria and most of whom (more than 78%) live in India [
2].
The emergence of drug resistance is reducing the therapeutic arsenal for the treatment of malaria at a rate that is barely balanced by the development of novel effective drugs. In this regard medicinal plant research has become more important particularly after the development of Chinese anti-malarial drug artemisinin, isolated from
Artemisia annua, a drug from traditional medicinal plants [
3,
4]. Natural plant products are main sources of biologically active compounds and have potential for the development of novel anti-malarial drugs. More recently a number of studies have been undertaken to evaluate the inhibitory effects of various plant extracts on
Plasmodium falciparum[
5,
6] and
Plasmodium berghei[
7,
8].
Two plants
Holarrhena antidysenterica (Apocynaceae) and
Viola canescens (Violaceae) commonly used as traditional medicine in the Garhwal region of north-west Himalaya for the treatment of protozoan infections and fever including malaria were studied. The stem bark of the
H. antidysenterica plant, commercially known as kurchi and kutaz in the Indian subcontinent has been investigated due to its traditional use in the treatment of amoebic dysentery, diarrhoea, asthma, bronchopneumonia [
9,
10]. In addition the plant has been reported to possess anti-helminthic, appetizing, anti-diarrhoeal, astringent properties [
11], used as an immunomodulating agent [
12], larval growth inhibitor [
13] and against vaginitis [
14]. Gaur [
15] reported that the bark of the
H. antidysenterica is used against malaria in the Garhwal region of north-west Himalaya. The other plant,
V. canescens commonly known as Gull-e-Banafsha and Himalayan White Violet in Indian herbal market is a nearly prostrate herb found at altitudes of 1,500-2,400 m in the Himalayan region. The plant is extensively used against cough, fever and malaria [
15].
These plants were tested for their in vitro and in vivo anti-malarial activity. In order to determine the selective indexes, cytotoxic activities of these plants were also studied.
Methods
Collection of plants
Based on ethnophamocological and ethnobotanical literature [
15] plants were collected during flowering season of year 2008 from the Garhwal region (
H. antidysenterica from Cheela range and
V. canescens from Chamba) and identified by Botanical Survey of India, Dehradun, India. Voucher specimens of the plants were stored in the Institute herbarium (voucher specimen numbers NIMRHAR-101-VC for
V. canescens and NIMRHAR-101-HA) for future reference.
The collected plants were washed with distilled water and dried on absorbing paper at an ambient temperature (25-30°C) in open air under shade for 5-10 days. The dry plants samples were ground to powder and stored at ambient temperature until use. For each plant, four types of extracts were prepared (petroleum ether, chloroform, methanol and water) in accordance with the increasing polarity of these solvents. The extracts were prepared by maceration of the plant material in the solvent at room temperature (50 g of powder in 150 ml of solvent) for three successive periods of three days, with a change of solvent every two days and then concentrated under reduced pressure. All extracts were tested for their residual solvents by GCMS analysis and solvent free extracts were screened for anti-malarial activity (in vitro and in vivo).
In vitro anti-plasmodial sensitivity against P. falciparum isolates
In vitro anti-plasmodial sensitivity of plant extracts was assessed at National Institute of Malaria Research, Dwarka, New Delhi, India using the procedure of Trager and Jensen [
16]. These extracts were also sent to WHO, Switzerland for screening of
in vitro anti-plasmodial activity using the parasite lactate dehydrogenase (pLDH) assay developed earlier [
17].
Plasmodium falciparum chloroquine sensitive strain FSG derived from an Indian patient of Shahjahanpur (UP) was used for the study using
in vitro candle-jar method. Culture was maintained in A +ve erythrocytes using RPMI 1640 medium supplemented with AB Rh +ve human serum (10%), sodium bicarbonate (0.2%), HEPES buffer (25 mM) and gentamycin (50 μg ml
-1). The culture was treated with selected concentrations of extracts. Blood smears were prepared and stained with Giemsa strain after 72 hrs of incubation % maturation of schizonts against control was recorded. Chloroquine was taken as positive control. The inhibitory concentration value, kills 50% of the parasites (IC
50) was considered for anti-plasmodial activity. For the parasite lactate dehydrogenase (pLDH) assay, chloroquine sensitive GHA strain derived from a Ghanaian patient was used and maintained in RPMI 1640 medium supplemented with 0.37 mM hypoxanthine, 25 mM HEPES, 25 mM NaHCO
3 and 10% A+ve human serum together with 2-4% washed human O +ve erythrocytes. All cultures and assays were conducted at 37 ± 1°C and an atmosphere of 4% carbon dioxide, 3% oxygen and 93% nitrogen. Assays were performed in sterile 384- well microtiter plates, each well containing 2 μl of compound solution (selected concentration) with 38 μl of the parasite inoculums (1% parasitaemia, 2% haematocrit). Parasite growth was compared to control wells (100% parasite growth). Plates were deep-frozen at -20°C, after 72 h of incubation at 37 ± 1°C. After thawing 5 μl from each well was transferred into another plate together with 25 μl of Malstat ™ reagent and 5 μl of a 1/1 mixture of PES (phenazine ethosulfate, 2 mg/ml) and NBT (Nitro Blue Tetrazolium Grade III, 0.1 mg/ml). The plates were then kept out of light for 2 h and the change in colour was measured with a spectrophotometer at 655 nm. The results were expressed as percent reduction in parasitaemia compared to control wells. Chloroquine was taken as positive control.
In vivo anti-malarial sensitivity against P. berghei
The test described by Peters [
18] for anti-malarial activity against a chloroquine sensitive
P. berghei NK65 strain in Swiss albino mice was used for monitoring
in vivo anti-malarial activity of extracts coded as VC-1 and HA-2. The protocol was approved by the animal ethical committee of the National Institute of Malaria Research, Delhi, India and the experiments were performed under the supervision of a veterinary doctor. The infected erythrocytes were injected intraperitonially (1 × 10
7 parasite per mouse) on day 0. The drug was administered intraperitonially for four consecutive days from day 0 to day 3 (10-30 mg/kg) in the experimental group. The control group was given the solvent (DMSO) in equal volume for the same duration. On day 4, tail blood smears were prepared, stained and percent parasitaemia was recorded. The suppression of parasitaemia in experimental group as compared to control group was calculated. Chloroquine was taken as positive control. The suppression of parasitaemia in relation to the control was assessed using the formula by Obih
et al[
19].
Cytotoxicity on rat skeletal muscle myoblasts (L-6 Cells)
The cytotoxicity of the examined extracts was determined using method reported earlier [
20,
21]. Rat skeletal muscle myoblasts, cell line L-6, were seeded in 96-well Costar microtiter plates at 2 × 103/cells/100 ml, 50 ml per well in MEM supplemented with 10% heat inactivated FBS. A three-fold serial dilution ranging from 90 to 0.13 mg/ml of compounds in test medium was added. Plates with a final volume of 100 ml per well were incubated at 37 1C for 72 h in a humidified incubator containing 5% CO
2. Resazurin was added as viability indicator. After an additional 2 h of incubation, the plate was measured with a fluorescence scanner using an excitation wavelength of 536 nm and an emission wavelength of 588 nm (SpectraMax GeminiXS, Molecular Devices).
Data analysis
Collected data from in vivo anti-malarial activity were subjected to analysis of Variance (ANOVA) by Scheffe's procedure using the software StatPlus 2009 Professional.
Discussion
Recently interest has been observed in the screening of plant derived extracts for their anti-malarial activity in order to develop herbal drug against malaria related to traditional medicine. Okokon and Nwafor [
22] have demonstrated 75% reduction on 54 mg/kg dose in parasitaemia in mice treated with chloroform extract of
Croton zambesicus which confirms the folkloric use of this plant in towns of Nigeria.
The plants used in our study were collected from different places in the Garhwal region, where they are being used by the local inhabitants to prepare herbal medicaments. As the Garhwal region covers a wide range of herbs and shrubs approximately 18,440 species of plants and some of them showed good
in vivo anti-plasmodial activity [
23]. The present investigation demonstrates the anti-plasmodial activities of petroleum ether and chloroform extracts of two plants from this region in
P. berghei infected mice. Treatment with the chloroform
H. antidysenterica bark extract significantly inhibited parasitaemia compared to no treatment. Simonsen and collaborators [
24] found that ethanolic bark crude extract of
H. antidysenterica had
in vitro anti-plasmodial activity against chloroquine susceptible strain of
P. falciparum with its IC
50 value of 28 μg/ml, while in present study chloroform extract of
H. antidysenterica was found active against
P. falciparum isolates (Table
2).
These results are comparable to extracts of some plants [
22,
25]. On the basis of more reproducible inhibition with chloroform extract of
H. antidysenterica, assessed for its
in vivo anti-malarial activity along with cytotoxicity. Percentage suppression of parasitaemia in mice treated with HA-2 extracts showed 70.2% at 30 mg/kg dose (Table
2) with the ED
50 value of 18.29 mg/kg, indicative of anti-plasmodial potential. Steroidal alkaloids of the conaine and aminopregnane types and the principal one being conessine from the stem bark of
H. antidysenterica was reported previously [
26]. Zirihi and co-workers [
27] evaluated
in vitro anti-plasmodial activity of conessine from the plant
Funtumia elastica against chloroquine-resistant strain FcB1 of
P. falciparum and cytotoxity against a rat cell line L-6 with its IC
50 1.04 μg/ml and 14 μg/ml respectively. The presence of conessine as leading compound may be responsible for the anti-malarial activity of extract HA-2.
In case of
V. canescens treatment with the petroleum ether extract inhibits parasitaemia significantly compared to that of control. However
V. canescens which is used against malaria in the Garhwal region has not been investigated till now. The petroleum ether extract of
V. canescens whole plant extract showed slightly cytotoxic effect against L-6 cells of rat skeletal myoblast (IC
50 12.39 μg/ml) and the inhibition of parasite growth of
P. falciparum (IC
50 2.76 μg/ml). Similarly petroleum ether extracts of
Viola websteri Hemsl (Violaceae) were reported to have anti-plasmodial activity against
P. falciparum in-vitro[
28]. VC-1 is evaluated for its
in vivo anti-malarial activity in
P. berghei infected Swiss albino mice as it showed significant anti-plasmodial activity against
P. falciparum isolate. The percent reduction of parasitaemia of VC-1 extract was found 63% at 20 mg/kg dose with the ED
50 value of 15.8 mg/kg against
P. berghei infected mice (Table
2). Results from
in vivo anti-malarial activity revealed that VC-1 showed significant reduction of parasitaemia on dose ranges 10-20 mg/kg. Where as on administration of the dose of 30 mg/kg of VC-1, weight loss was recorded in some mice and 30% of the mice were died with in 10 days.
Acknowledgements
The authors thankfully acknowledge the financial support of the Uttarakhand State Council for Science and Technology (UCOST), Dehradun, India and UNDP/WHO special programme for Research and Training in Tropical Diseases (TDR) for the in vitro screening of anti-plasmodial activities. We are also expressing our sincere gratitude to Dr. Reto Brun and Dr. Marcel Kaiser, WHO, Geneva for their comments on the manuscript.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
GV (PhD student) contributed in the laboratory work, analysis of the data and drafted the paper. VKD and DDA designed the work and supervised the in vitro and in vivo studies and analysed the data. PKA performed the in vivo studies. All authors contributed to the critical review of the manuscript and agree to submission.