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使用**[具体测试名称]**试验,比较(施莱希特)博伊斯提取物和异丁质环氧化物与氯喹对**[疟原虫名称]**的抗疟效果评估。

Evaluation of the Antimalarial Effect of (Schlecht.) Boiss. Extract and Suberosin Epoxide Against in Comparison with Chloroquine Using Test.

作者信息

Sajjadi Seyed Ebrahim, Pestechian Nader, Kazemi Mahnaz, Mohaghegh Mohammad-Ali, Hosseini-Safa Ahmad

机构信息

Department of Pharmacognosy, School of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran.

Department of Parasitology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Iran J Pharm Res. 2016 Summer;15(3):515-521.

Abstract

Resistance to most antimalarial drugs has encouraged the development of novel drugs. An alternative source for discovering such drugs is natural products. Some species are used in folk medicine for their sedative, tonic and anti-parasitic effects. Besides, coumarins isolated from this genus found to have in vitro anti-leishmanicidal effect. The present study is aimed to evaluate the antimalarial activity of (Schlecht.) Boiss. extract and suberosin epoxide, using suarian mice. A rodent malaria parasite, was used to inoculate healthy male Swiss Albino mice of age 6-8 weeks and weight 23-27 g. Hydro-alcoholic extract of (20, 100, 300, 600 mg/Kg) and suberosin epoxide suspension (10, 30, 50, 100 mg/Kg) were administered subcutaneously. Parameters including percentage of parasitemia, suppression of parasitemia and mean survival time were determined using standard test such as peters. Chemo-protective effects were exerted by the crude extract and suberosin epoxide. Maximum effect was observed with the larger doses of the crude extract and suberosin epoxide. Suberosin epoxide increased the survival time compared to chloroquine. However, the results of this study indicate that the plant has a promising anti-plasmodial activity against . Thus, it could be considered as a potential source of new antimalarial agents. Suberosin epoxide at the dose of 100 mg/Kg possesses relatively significant antimalarial effect. Chemical derivatization of the parent compound or preparation of the modified formulation is required to improve its systemic bioavailability.

摘要

对大多数抗疟药物的耐药性促使了新型药物的研发。发现此类药物的另一个来源是天然产物。一些物种因其镇静、滋补和抗寄生虫作用而被用于民间医学。此外,从该属中分离出的香豆素具有体外抗利什曼原虫的作用。本研究旨在使用叙利亚小鼠评估(Schlecht.)Boiss.提取物和环氧化苏伯脂素的抗疟活性。使用一种啮齿动物疟原虫感染6 - 8周龄、体重23 - 27克的健康雄性瑞士白化小鼠。皮下注射(20、100、300、600毫克/千克)的水醇提取物和环氧化苏伯脂素悬浮液(10、30、50、100毫克/千克)。使用彼得斯等标准试验测定包括疟原虫血症百分比、疟原虫血症抑制率和平均存活时间等参数。粗提取物和环氧化苏伯脂素发挥了化学保护作用。粗提取物和环氧化苏伯脂素剂量越大,效果越明显。与氯喹相比,环氧化苏伯脂素延长了存活时间。然而,本研究结果表明该植物对具有有前景的抗疟原虫活性。因此,它可被视为新抗疟药物的潜在来源。100毫克/千克剂量的环氧化苏伯脂素具有相对显著的抗疟作用。需要对母体化合物进行化学衍生或制备改良制剂以提高其全身生物利用度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47cf/5149039/67c7ba610515/ijpr-15-515-g001.jpg

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