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评价. 的抗疟活性:一种 和一种 方法。

Evaluation of Antimalarial Activity of Ethanolic Extract of .: An and an Approach.

机构信息

Department of Biochemistry, College of Pure and Applied Science, Landmark University, Omu-Aran, Kwara State, Nigeria.

Department of Biochemistry, Faculty of Life Science, 108285University of Ilorin, Ilorin, Nigeria.

出版信息

J Evid Based Integr Med. 2023 Jan-Dec;28:2515690X231165104. doi: 10.1177/2515690X231165104.

Abstract

In Nigeria, L. has been used to treat a variety of ailments. The mechanism of the antimalarial activity of ethanolic leaf extract of (EEAML) was investigated using both an in vivo and an in silico approach. The experimental mice were divided into five groups: A-F. The mice in groups B-F were inoculated with NK-65 and treated accordingly. Groups A and B are the negative and positive controls (infected and untreated), respectively. Group C received 10 mg/kg chloroquine (standard drug), whereas groups D-F received 100, 200, and 300 mg/kg body weight of the extract orally respectively. The mice were euthanized eight days after infection, and their liver and blood were collected and used in biochemical tests. Molecular docking was performed using the extract's HPLC compounds and proteins. In the suppressive, prophylactic, and curative tests, there was a significant decrease (p < 0.05) in parasitemia levels in groups treated with the extract compared to the positive control and standard drug. When compared to the positive control, there was a significant (p < 0.05) reduction in liver MDA, total cholesterol, and total triglyceride levels. The binding energies of luteolin and apigenin-protein complexes were significantly (p < 0.05) higher compared to their respective references. The anti-plasmodial activity of the extract may result from its hypolipidemic effect, which deprives the parasite of essential lipid molecules needed for parasite growth, as well as from the inhibitory effects of apigenin and luteolin on specific proteins required for the metabolic pathway.

摘要

在尼日利亚,已使用 L 来治疗各种疾病。采用体内和计算两种方法研究了(EEAML)乙醇叶提取物的抗疟活性的机制。将实验小鼠分为五组:A-F。B-F 组的小鼠接种了 NK-65 并进行了相应的处理。A 组和 B 组分别为阴性和阳性对照(感染和未处理)。C 组给予 10mg/kg 氯喹(标准药物),而 D-F 组分别给予 100、200 和 300mg/kg 体重的提取物口服。感染后 8 天处死小鼠,收集其肝脏和血液并用于生化测试。使用提取物的 HPLC 化合物和蛋白质进行分子对接。在抑制、预防和治疗试验中,与阳性对照和标准药物相比,用提取物处理的组的寄生虫血症水平显着降低(p<0.05)。与阳性对照相比,肝脏 MDA、总胆固醇和总甘油三酯水平显着降低(p<0.05)。木犀草素和芹菜素-蛋白质复合物的结合能显着(p<0.05)高于各自的参考值。提取物的抗疟活性可能是由于其降血脂作用,这种作用剥夺了寄生虫生长所需的必需脂质分子,以及芹菜素和木犀草素对代谢途径所需的特定蛋白质的抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6a2/10084581/3ba7720ba8ca/10.1177_2515690X231165104-fig1.jpg

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