ANTITRYPANOSOMAL POTENTIAL OF BUCHHOLZIA CORIACEA SEED EXTRACTS IN MICE

Oluwaferanmi Adefolaju, A. Abubakar
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Abstract

Buchholzia coriacea seed extracts were screened for possible anti-trypanosomal activity in mice. Whole Buchholzia coriacea seed was successively extracted with 80% ethanol (EtOH) and partitioned in petroleum ether and ethyl acetate to obtained crude extracts. The flavonoid was extracted from crude ethanol extract using column chromatography. The crude extracts and flavonoids obtained were screened for in vivo antitrypanosomal activity. In the in vivo study, both the crudes and flavonoids extracts were separately orally administered to Trypanosomal brucei brucei infected mice after the establishment of parasitaemia. The animals were grouped into 9 groups of 4 mice each and were treated with respective dose levels as follows: Group 1 (Crude 1000mg/kg), Group 2 (Residue 1000mg/kg), Group 3 (Petroleum ether 1000mg/kg), Group 4 (Ethyl acetate 1000mg/kg), Group 5 (Flavonoid 500mg/kg), Group 6 (Flavonoid 1000mg/kg), Group 7 (Positive control, uninfected, untreated), Group 8 (Negative control, infected untreated) and Group 9 (Infected and treated with Berenil®. The body weights of all the animals were determined at pre and post treatment. Both qualitative and quantitative phytochemical analysis of the crude plant extract was also carried out. The in vivo results showed that the flavonoid extract gave the highest prolongation of life by 9 days when compared to its crude counterparts by 6 days at 1000 mg/kg body weight (P<0.05). All the treated animals suffered less weight lost as compared to the infected untreated control. Phytochemical screening of the extract revealed the presence of flavonoid, alkaloid, tannins, glycosides, terpenes, and phenols with Tannins quantitatively being the highest followed by flavonoids. Consequently, flavonoid from B. coriacea is an antitrypanosomal potential and could further be exploited for drug development in the management of African trypanosomiasis.
鹿茸种子提取物对小鼠抗锥虫体的作用
筛选了芫荽籽提取物在小鼠体内可能的抗锥虫活性。用80%乙醇(EtOH)提取整个鹿皮籽,再用石油醚和乙酸乙酯进行分割,得到粗提物。采用柱层析法从粗乙醇提取物中提取黄酮类化合物。对得到的粗提物和黄酮类化合物进行体内抗锥虫活性筛选。在体内研究中,在建立寄生虫病后,将粗提物和黄酮类提取物分别口服给感染布鲁氏锥虫的小鼠。将实验动物分为9组,每组4只,分别按剂量处理:1组(粗1000mg/kg)、2组(残留1000mg/kg)、3组(石油醚1000mg/kg)、4组(乙酸乙酯1000mg/kg)、5组(类黄酮500mg/kg)、6组(类黄酮1000mg/kg)、7组(阳性对照,未感染,未处理)、8组(阴性对照,未感染,未处理)、9组(感染,用Berenil®处理)。测定各组动物治疗前后的体重。对粗提取物进行了定性和定量的植物化学分析。体内试验结果表明,在1000 mg/kg体重时,黄酮类提取物的寿命比粗提取物的寿命延长6天,最高可延长9天(P<0.05)。与未接受治疗的对照组相比,所有接受治疗的动物体重减轻的幅度都较小。植物化学筛选结果显示,黄酮类化合物主要有黄酮类、生物碱类、单宁类、苷类、萜烯类和酚类,单宁类含量最高,其次是黄酮类。因此,马鞭草类黄酮具有抗锥虫的潜力,可以进一步开发用于治疗非洲锥虫病的药物开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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