Ethanol extract of Bergenia ciliata (Haw.) Sternb. (rhizome) impedes the propagation of the malaria parasite

被引:1
|
作者
Gorki, Varun [1 ]
Walter, Neha Sylvia [1 ]
Chauhan, Monika [2 ]
Kaur, Manninder [3 ]
Dhingra, Neelima [2 ]
Bagai, Upma [1 ]
Kaur, Sukhbir [1 ]
机构
[1] Panjab Univ, Dept Zool, Parasitol Lab, Chandigarh 160014, India
[2] Panjab Univ, Univ Inst Pharmaceut Sci, Chandigarh, India
[3] Panjab Univ, Ctr Stem Cell & Tissue Engn, Chandigarh, India
关键词
Malaria; Traditional medicinal plants; Bergenia ciliata; Antimalarial activity; HPTLC; VITRO ANTIMALARIAL ACTIVITY; GALLIC ACID; SOLUBILITY; (+)-CATECHIN; PLANTS; WATER;
D O I
10.1016/j.jep.2021.114417
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: The increasing resistant cases even against artemisinin-based combination therapy have necessitated the need to develop new antimalarials. Phytomedicinal therapy is a benchmark for malaria in the Himalayan region. As the dialect and traditional variations have been seen along with this, usage of medicinal plant, its portion (shoot and root system) and mode of preparation also varies. There is no scientific evidence available for illustrating the antiplasmodial activity of the rhizomes of Bergenia ciliata (Saxifragaceae), which is known to be an antipyretic (fever akin to malaria), hepato-protective, and also for spleen enlargement. Aim of the study: The present study evaluates the antimalarial activity of ethanol extract of B. ciliata rhizomes (EREBC). Materials and methods: HPTLC was performed to identify and quantify three marker compounds in EREBC. The in vitro antimalarial activity was evaluated by schizont maturation inhibition assay. MTT assay was employed to test the cytotoxicity of EREBC. Peter's 4-day test and Peters method was employed to discern the suppressive and preventive activity of the extract respectively. Results: HPTLC analysis revealed the presence of bergenin, epicatechin and gallic acid in the extract. EREBC exhibited considerable inhibition (IC50 < 5 mu g/mL) of schizont maturation of both RKL-9 and MRC-2 strains of P. falciparum. EREBC was non-toxic to both HeLa cells and normal dermal fibroblasts (CC50 > 1000 mu g/mL). The selectivity index was > 200 for both strains. Acute toxicity of EREBC was > 4 g/kg. EREBC exhibited consid-erable in vivo suppressive activity with 96.48% inhibition at 500 mg/kg in comparison to chloroquine (96.08%). The ED50 of the extract was < 50 mg/kg. No mortality was evident in mice administered with different doses of EREBC (50-500 mg/kg) throughout the follow up period of 28 days. EREBC exhibited safety to liver and kidney function of mice as observed from biochemical analysis. Conclusion: Overall, the study illustrates the marked efficacy and potential of EREBC as an antimalarial agent with bergenin, epicatechin and gallic acid its major constituents, which played a pivotal role in the generation of the immune response.
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页数:13
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