乙醇性苦艾叶提取物和甲醇性苦艾种子抗肾上腺浆电位的研究

G. Batiha, A. M. Beshbishy, D. S. Tayebwa, O. Adeyemi, N. Yokoyama, I. Igarashi
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引用次数: 14

摘要

针对螺形体病的现有药物不足,并面临一些挑战,如耐药寄生虫和对治疗动物的毒性。因此,发现新的药物化合物是有效控制巴贝斯虫病及其菌痢的必要条件。甲醇性苦艾籽提取物(MPHSE)和乙醇性苦艾叶提取物(EAALE)具有多种药用特性。本研究在体外和体内对MPHSE和EAALE的生长抑制作用进行了评价。MPHSE对牛巴贝斯虫、双歧巴贝斯虫、发散巴贝斯虫、caballi巴贝斯虫和马氏巴贝斯虫的半最大抑制浓度(IC50)分别为24.9±1.2、77.1±2.3、61.1±2.9、80.8±4.1和11.3±2.1 μg/mL。EAALE对牛b、双头b、发散b、caballi和equi的IC50值分别为43.3±3.1、39.2±2.7、38.5±3.7、50.3±2.1和28.2±2.1 μg/mL。对牛Madin-Darby肾(MDBK)、小鼠胚胎成纤维细胞(NIH/3T3)和人包皮成纤维细胞(HFF)的毒性实验表明,MPHSE对MDBK、NIH/3T3和HFF细胞的半数最大有效浓度(EC50)分别为611.7±10.9、870±22和1500 μg/mL, EAALE对MDBK、NIH/3T3和HFF细胞的EC50分别为340.7±8.5、736.7±9.3和1371.5±17.3 μg/mL。在体内实验中,150 mg/kg的MPHSE和EAALE口服处理对小鼠微巴贝斯虫生长的抑制作用分别为60%和55.1%。这些发现表明,MPHSE和EAALE有可能成为治疗螺形体病的替代疗法。
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Anti-piroplasmic potential of the methanolic Peganum harmala seeds and ethanolic Artemisia absinthium leaf extracts
The available drugs against piroplasmosis are insufficient and faced with several challenges, such as drug-resistant parasites and toxicity to treated animals. Therefore, the discovery of new drug compounds is necessary for the effective control of babesiosis and theileriosis. Methanolic Peganum harmala seed extract (MPHSE) and ethanolic Artemisia absinthium leaf extract (EAALE) have several medicinal properties. In the present study, the growth-inhibition effects of MPHSE and EAALE were evaluated in vitro and in vivo. The half-maximal inhibitory concentration (IC50) values for MPHSE against Babesia bovis, B. bigemina, B. divergens, B. caballi, and Theileria equi were 24.9 ± 1.2, 77.1 ± 2.3, 61.1 ± 2.9, 80.8 ± 4.1, and 11.3 ± 2.1 μg/mL, respectively. EAALE exhibited IC50 values of 43.3 ± 3.1, 39.2 ± 2.7, 38.5 ±3.7, 50.3 ± 2.1, and 28.2 ± 2.1 μg/mL against B. bovis, B. bigemina, B. divergens, B. caballi, and T. equi, respectively. The toxicity assay on Madin–Darby bovine kidney (MDBK), mouse embryonic fibroblast (NIH/3T3), and human foreskin fibroblast (HFF) cell lines showed that MPHSE affected the viability of MDBK, NIH/3T3, and HFF cell lines with half maximum effective concentration (EC50) values of 611.7± 10.9, 870 ± 22, and ˃1500 μg/mL, respectively, while EAALE exhibited EC50 values of 340.7 ± 8.5, 736.7 ± 9.3, and 1371.5 ± 17.3 μg/mL against MDBK, NIH/3T3, and HFF cell lines, respectively. In the in vivo experiment, MPHSE and EAALE oral treatments at 150 mg/kg inhibited the growth of Babesia microti in mice by 60% and 55.1%, respectively. These findings suggest that MPHSE and EAALE have the potential to be alternative remedies for treating piroplasmosis.
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