Nureye Dejen, Sano Muktar, Fekadu Mesfin, Duguma Tadesse, Tekalign Eyob
Department of Pharmacology and Toxicology, School of Pharmacy, College of Medicine and Health Sciences, Mizan-Tepi University, P.O. Box 260, Mizan-Aman, Ethiopia.
Department of Pharmacy, College of Health Sciences, Arsi University, P.O. Box 193, Asella, Ethiopia.
Evid Based Complement Alternat Med. 2021 Sep 1;2021:9625169. doi: 10.1155/2021/9625169. eCollection 2021.
The evolution of resistance to currently used malaria medicines together with the severe economic burden of malaria initiates the search for novel antimalarial drugs. Thus, the present experiment was intended to assess the antiplasmodial effect of based on the traditional claims and in vitro antimalarial effect of the plant.
For the crude extraction of stem barks of , a cold maceration method using hydromethanol as a solvent was employed. The hydroalcoholic extract was then fractionated by three solvents (chloroform, n-butanol, and aqueous solvent) with different polarity indexes. Swiss albino mice infected with the chloroquine-sensitive malaria parasite () were used in this study. Acute oral toxicity study was done according to standard protocols. Four-day suppressive (hydromethanolic crude extract and solvent fractions), Rane's (crude extract), and repository (crude extract) tests were used to examine the antiplasmodial effects of the study plant.
The chemosuppressive study revealed that all doses of the crude extract and its fractions displayed a significant ( < 0.001) inhibition of parasitemia compared with the vehicle (negative control). The crude extract's highest dose (600 mg/kg) showed the maximum (57.84%) parasitemia suppression during the chemosuppressive test. The crude extract also produced significant ( < 0.001) curative and prophylactic effects at all doses in Rane's and repository tests compared with the negative control. In the 4-day test, the n-butanol fraction produced parasitemia suppression higher than the chloroform fraction but lower than the crude extract. Of these, water fractions demonstrated the lowest chemosuppressive effect. Anthraquinone, alkaloids, flavonoids, saponins, steroids, tannins, and terpenoids were qualitatively detected in the plant material.
The current results showed that the hydromethanolic extract and fractions of stem barks have antiplasmodial action with a high curative effect. Chloroform and n-butanol fractions were more active among the fractions, indicating that the nonpolar and semipolar constituents of the plant are responsible for the antimalarial effects.
对当前使用的疟疾药物的耐药性演变以及疟疾带来的沉重经济负担促使人们寻找新型抗疟药物。因此,本实验旨在根据传统说法以及该植物的体外抗疟作用来评估其抗疟效果。
对于[植物名称]茎皮的粗提物,采用以氢甲醇为溶剂的冷浸法。然后用三种具有不同极性指数的溶剂(氯仿、正丁醇和水性溶剂)对水醇提取物进行分离。本研究使用感染了氯喹敏感疟原虫([疟原虫名称])的瑞士白化小鼠。根据标准方案进行急性口服毒性研究。采用四天抑制试验(氢甲醇粗提物和溶剂分离物)、雷氏试验(粗提物)和储存试验(粗提物)来检测受试植物的抗疟效果。
化学抑制研究表明,与赋形剂(阴性对照)相比,粗提物及其所有剂量的分离物对疟原虫血症均表现出显著(<0.001)抑制作用。粗提物的最高剂量(600mg/kg)在化学抑制试验中显示出最大的疟原虫血症抑制率(57.84%)。与阴性对照相比,粗提物在雷氏试验和储存试验的所有剂量下也都产生了显著(<0.001)的治疗和预防效果。在四天试验中,正丁醇分离物产生的疟原虫血症抑制作用高于氯仿分离物,但低于粗提物。其中,水分离物的化学抑制作用最低。在植物材料中定性检测到了蒽醌、生物碱、黄酮类、皂苷、甾体、单宁和萜类化合物。
当前结果表明,[植物名称]茎皮的氢甲醇提取物及其分离物具有抗疟作用,且疗效显著。氯仿和正丁醇分离物在分离物中活性更高,表明该植物的非极性和半极性成分具有抗疟作用。