毛缕草叶提取物体外抗恶性疟原虫和体内抗伯格氏疟原虫的研究

N. Walter, U. Bagai
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引用次数: 5

摘要

目的:利用传统药用植物毛根草对恶性疟原虫的体外抗疟原虫活性和体内对伯氏疟原虫的防治活性进行评价。研究了毛缕草叶乙醇提取物(ELEBC)对小鼠肝肾功能的影响。研究地点和时间:2014年10月至2015年11月,印度昌迪加尔,旁遮普大学动物学系寄生虫学实验室。方法:采用WHO方法评价ELEBC对恶性疟原虫耐氯喹(RKL-9)和敏感(MRC-2)菌株的体外抗疟原虫活性。采用MTT法、Walter法和Bagai法测定了该提取物对人肿瘤和正常细胞株的细胞毒性;中国生物医学工程学报,17(6):1-10,2016;文章no.BMRJ。29262 2测定。采用Peter法、Ryley改良法和Peters改良法分别测定其体内储存量和对伯氏黑螺旋体的疗效。生化试验按标准方法进行。结果:ELEBC对恶性疟原虫RKL-9和MRC-2株均有较强的抑制活性,IC50分别为6.4和1000 μg/ml,选择性指数(SI) >10。在第7天,浓度为1000 mg/kg(储存库活性)和250 mg/kg(治疗活性)时,最大化学抑制率分别为74.45%和91.96%。G6 (750 mg/kg)组小鼠存活率为83.33%,其余ELEBC组小鼠治疗试验第28天存活率为50%。血清肝功能(SGOT、SGPT、ALP和胆红素)和肾功能生物标志物(肌酐和尿素)均显著低于感染对照组(G2)。结论:ELEBC对恶性疟原虫敏感株和耐药株均具有较强的抗疟活性。它作为一种预防和治疗疾病的药物也显示出显著的疗效,对啮齿动物宿主的肝肾功能没有任何副作用。
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Antimalarial Efficacy of Bergenia ciliata (Saxifragaceae) Leaf Extract In vitro against Plasmodium falciparum and In vivo against Plasmodium berghei
Aim: The traditional medicinal plant Bergenia ciliata was used to evaluate its antiplasmodial activity against Plasmodium falciparum in vitro and preventive and curative activity against Plasmodium berghei in vivo. The safety of the ethanolic leaf extract of Bergenia ciliata (ELEBC) to the liver and kidney functions of the rodent host was also tested. Place and Duration of the Study: Parasitology Laboratory, Department of Zoology, Panjab University, Chandigarh, India, between October 2014 to November 2015. Methodology: The in vitro antiplasmodial activity of the ELEBC against both chloroquine-resistant (RKL-9) and sensitive (MRC-2) strains of P. falciparum was assessed by using the WHO method. The cytotoxicity of the extract against human cancer and normal cell lines was tested by MTT Original Research Article Walter and Bagai; BMRJ, 17(6): 1-10, 2016; Article no.BMRJ.29262 2 assay. The in vivo repository and curative efficacy of the extract against P. berghei were tested using the Peter’s method and modified method of Ryley and Peters respectively. The biochemical assays were performed as per standard methods. Results: ELEBC exhibited considerable inhibitory activity against both RKL-9 and MRC-2 strains of P. falciparum with IC50 of 6.4 μg/ml and <5 μg/ml respectively. The extract exhibited no toxicity against both cancer and normal cell lines with CC50 >1000 μg/ml and selectivity index (SI) >10. Maximum chemosuppression of 74.45% and 91.96% was observed on day 7 at a concentration of 1000 mg/kg (repository activity) and 250 mg/kg (curative activity), respectively. 83.33% survival of mice was observed in G6 (750 mg/kg) while in all other ELEBC treated groups 50% survival was recorded on day 28 of study in the curative test. Hepatic function (SGOT, SGPT, ALP and bilirubin) and renal function biomarkers (creatinine and urea) in serum were observed to be significantly (P< 0.0005) lower as compared to the infected control (G2). Conclusions: ELEBC possesses considerable antimalarial activity against both sensitive and resistant strains of P. falciparum. It also exhibits significant efficacy as a preventive and curative remedy against the disease without any side effects on hepatic and renal functions of the rodent host.
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