Girma Biruktawit, Bisrat Daniel, Asres Kaleab
Department of Pharmaceutical Chemistry and Pharmacognosy, School of Pharmacy, Addis Ababa University, Addis Ababa, Ethiopia.
Anc Sci Life. 2015 Jan-Mar;34(3):142-6. doi: 10.4103/0257-7941.157158.
Malaria is one of the major obstacles to the socioeconomic development of several developing countries. Adequate treatment of the disease is becoming increasingly difficult due to the worsening problems of drug resistance in many parts of the world. Therefore, increased efforts in antimalarial drug discovery are urgently needed.
This study was designed to evaluate the antimalarial activity of the leaf latex of Aloe citrina Carter and Brandham and its major constituent.
The leaf latex of A. citrina was dissolved in methanol and subjected to preparative thin layer chromatography. Structure of the isolated compound was determined on the basis of its electrospray-ionization tandem mass spectrometry, (1)H, (13)C NMR and DEPT spectral data. The latex and its isolated compound were tested for their in vivo antimalarial activity using a 4-day suppressive test against chloroquine sensitive ANKA strain of Plasmodium berghei in mice.
Homonataloin A/B was isolated as a major component of the latex. Both the latex and isolated compound exhibited significant (P < 0.001) antimalarial activity at a dose of 400 mg/kg with parasite suppression of 60.59% and 67.52%, respectively. No significant adverse signs of toxicity were observed in mice treated with the leaf latex up to the highest dose (5000 mg/kg).
The results of this study indicate that the antimalarial activity of the plant is attributed in part or in full to the presence of homonataloin A/B in the latex. It also validates the traditional use of the plant as an antimalarial agent.
疟疾是几个发展中国家社会经济发展的主要障碍之一。由于世界许多地区耐药性问题日益严重,对该疾病进行充分治疗变得越来越困难。因此,迫切需要加大抗疟药物研发力度。
本研究旨在评估库拉索芦荟叶乳胶及其主要成分的抗疟活性。
将库拉索芦荟叶乳胶溶解于甲醇中,进行制备型薄层色谱分析。根据电喷雾电离串联质谱、(1)H、(13)C核磁共振和DEPT光谱数据确定分离出的化合物结构。使用对氯喹敏感的伯氏疟原虫ANKA株对小鼠进行为期4天的抑制试验,检测乳胶及其分离出的化合物的体内抗疟活性。
分离出高诺塔罗因A/B作为乳胶的主要成分。乳胶和分离出的化合物在剂量为400mg/kg时均表现出显著(P<0.001)的抗疟活性,寄生虫抑制率分别为60.59%和67.52%。在用叶乳胶处理的小鼠中,直至最高剂量(5000mg/kg)均未观察到明显的毒性不良反应。
本研究结果表明,该植物的抗疟活性部分或全部归因于乳胶中存在高诺塔罗因A/B。这也证实了该植物作为抗疟剂的传统用途。