Saleheen et al. (
10), have reported aqueous
A. cepa extracts (AOE) gave an IC
100 and average IC
50 values of 1.25 mg/mL and 0. 376 mg/mL, respectively, against tested
L. major promastigotes (
10). These figures are close to our finding in the present study. According to the mentioned reports above, the
L. major promastigotes inhibited by the ethanolic and methanolic extracts of
I. brachiata root had low viability (20%) while the
L. major promastigotes inhibited with aqueous
A. cepa extracts had high viability (80%). It was interesting to note that the ethanolic as well as methanolic extracts of
I. brachiata root and aqueous onion revealed potential leishmanicidal activity, as shown in Tabe1, with the IC
50 values of 0.078 and 1.25 mg/mL, respectively. These were comparable to the effects of glucantime (IC
50 = 21.25 mg/mL) used as positive control. The IC
100 values of tested plant extracts were 2.5-5.0 mg/mL, which were comparable to the IC
100 of 85 mg/mL glucantime. These results revealed that the the tested plant extracts had high potential antileishmanial activity in comparison to glucantime (IC
50 of 21.25 mg/mL and IC
100 of 85 mg/mL). However, according to the previous studies, some other plant extracts such as
Allium sativum,
Plagiochila disticha, and
Casearia sylvestris also have exhibited inhibitory activities against
Leishmania (
13). Moreover, the presence of compounds such as tannins, flavonoids, saponin carbohydrates, coumarins, and triterpenes reported by previous studies (
9), may be responsible for leishmanicidal activity in this plant. These results are supported with the observations of Marine et al. and Firdous et al. (
14,
15), who have shown the leishmanicidal activity of the flavonoids isolated from
Consolida oliveriana and the efficacy of the carbohydrates in treatment of leishmaniasis. In addition, tannins isolated from
Anogeissusleiocarpus was shown to possess a good activity against
Leishmania (
16). Other compound such as terpenoids (sesquiterpene lactones) have been reported to be active against
Leishmania (
17).
This study revealed that selected plants in this investigation contained potent compound with high potential leishmanicidal activity. Although glucantime is very toxic, it is still used because other drugs have been shown to be of variable effect or ineffective against the parasites (
18). Since commercial drugs for treatment of leishmaniasis have many side effects, it would be timely to find effective medicinal plants in herbal medicine for the investigation and isolation of their active compound and the study of their toxicity.