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体内抗疟评价马马麻汤对感染伯氏疟原虫的小鼠的影响。

In vivo antimalarial evaluation of MAMA decoction on Plasmodium berghei in mice.

机构信息

Department of Pharmacognosy, Obafemi Awolowo University, Ile-Ife, Nigeria,

出版信息

Parasitol Res. 2014 Feb;113(2):505-11. doi: 10.1007/s00436-013-3680-0. Epub 2013 Nov 22.

Abstract

The use of decoctions of different plant materials is common practice in antimalarial ethnomedicine in Africa. Scientific evaluation of such herbal combinations to verify the claims is important. The study has evaluated the antimalarial efficacy of MAMA decoction (MD), a multicomponent herbal preparation and its individual plant components, namely leaves of Morinda lucida Benth [Rubiaceae] (ML), Azadirachta indica A. Juss [Meliaceae] (AI), Alstonia boonei De Wild [Apocynaceae] (AB) and Mangifera indica L [Anacardiaceae] (MI) in Plasmodium berghei-infected mice. Each decoction was prepared by boiling the powdered leaf in water, concentrated in vacuo and freeze-dried. The acute toxicity of MD (LD50=3.8 g/kg) was determined using Lorke's method. The antimalarial activities of MD and its plant components were evaluated by oral administration of the freeze-dried extracts (15-240 mg/kg) using the early malaria infection test model. The established malaria infection test was used to evaluate MD (60-240 mg/kg) while amodiaquine [10 mg/kg] (AQ) and distilled water were employed as the positive and negative controls, respectively. From the early malaria infection test, the effective doses at 50 % (ED50) and 90 % (ED90) for MD, AB, AI, ML, MI and AQ were 43, 79, 140, 134, 208 and 3.9 mg/kg and 202, 276, 291, 408, 480 and 9.2 mg/kg, respectively. For the established infection test, MD (240 mg/kg) and AQ gave parasite clearance of 55 and 95 % on day 5 of treatment. MD possesses antimalarial activity and is relatively safe.

摘要

在非洲的抗疟民族医学中,使用不同植物材料的煎剂是一种常见做法。科学评估这些草药组合以验证其说法非常重要。本研究评估了 MAMA 煎剂(MD)、一种多成分草药制剂及其个别植物成分,即 Morinda lucida Benth [茜草科](ML)叶、Azadirachta indica A. Juss [楝科](AI)、Alstonia boonei De Wild [夹竹桃科](AB)和 Mangifera indica L [漆树科](MI)在伯氏疟原虫感染小鼠中的抗疟功效。每种煎剂均通过将粉末状叶片煮沸在水中、真空浓缩和冷冻干燥来制备。使用 Lorke 法测定 MD(LD50=3.8 g/kg)的急性毒性。通过口服冷冻干燥提取物(15-240 mg/kg)评估 MD 及其植物成分的抗疟活性,使用早期疟疾感染试验模型。使用已建立的疟疾感染试验评估 MD(60-240 mg/kg),而阿莫地喹[10 mg/kg](AQ)和蒸馏水分别用作阳性和阴性对照。从早期疟疾感染试验中,MD、AB、AI、ML、MI 和 AQ 的 50%有效剂量(ED50)和 90%有效剂量(ED90)分别为 43、79、140、134、208 和 3.9 mg/kg 和 202、276、291、408、480 和 9.2 mg/kg。对于已建立的感染试验,MD(240 mg/kg)和 AQ 在治疗第 5 天使寄生虫清除率分别达到 55%和 95%。MD 具有抗疟活性且相对安全。

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