Malan Dehan, Van Niekerk Suzanne, Häberli Cécile, Keiser Jennifer, Van der Kooy Frank
Centre of Excellence for Pharmaceutical Sciences (Pharmacen™), North-West University, Private Bag X6001, Potchefstroom 2520, South Africa.
Swiss Tropical and Public Health Institute, Kreuzstrasse 2 4123, Allschwil, Switzerland; University of Basel, Basel, Switzerland.
Acta Trop. 2025 Feb;262:107535. doi: 10.1016/j.actatropica.2025.107535. Epub 2025 Jan 23.
Praziquantel is currently the only effective treatment for schistosomiasis, but several limitations underscore the need for new therapeutic agents. Recent promising in vitro results with Artemisia species and the success of A. annua and its active compound artemisinin in treating parasitic infections warrant the need for further studies. Here we evaluate the in vitro activity of nine Artemisia species, including previously untested species, against newly transformed schistosomula (NTS) and adult Schistosoma mansoni. Three extracts were prepared: an aqueous infusion, a dichloromethane (DCM) fraction of the aqueous infusion, and a DCM extract. All samples were tested for activity at concentrations ranging from 1-25 μg/ml against NTS and the most promising against the adult S. mansoni. All aqueous infusions showed inferior activity against NTS as opposed to the DCM fractions of the infusions and DCM extracts of A. abrotanum, A. arborescens, A. afra, and A. scoparia which displayed superior activity as compared to the positive control praziquantel. The DCM fraction infusions of A. afra (BB) were the most active with IC values of 0.35 μg/ml against NTS and 4.5 μg/ml against adult worms. Chemical fingerprinting using High-performance liquid chromatography (HPLC) analysis of the samples revealed some phytochemical similarities and significant differences between the species tested. This study provides supporting evidence of the antischistosomal potential of Artemisia spp. and warrants more in-depth research to identify potential novel therapeutic agents for the treatment of schistosomiasis.
吡喹酮是目前治疗血吸虫病的唯一有效药物,但存在的一些局限性凸显了对新型治疗药物的需求。近期,蒿属植物在体外实验中取得了令人鼓舞的结果,青蒿及其活性化合物青蒿素在治疗寄生虫感染方面的成功,使得有必要进行进一步研究。在此,我们评估了9种蒿属植物(包括之前未测试过的物种)对新转化的血吸虫幼虫(NTS)和曼氏血吸虫成虫的体外活性。制备了三种提取物:水浸剂、水浸剂的二氯甲烷(DCM)馏分和DCM提取物。所有样品均在1-25μg/ml的浓度范围内测试对NTS的活性,并测试对曼氏血吸虫成虫最具前景的活性。与阳性对照吡喹酮相比,所有水浸剂对NTS的活性均较差,而南艾蒿、银蒿、南非蒿和石蒿的水浸剂的DCM馏分及DCM提取物表现出更高的活性。南非蒿(BB)的DCM馏分水浸剂活性最强,对NTS的IC值为0.35μg/ml,对成虫的IC值为4.5μg/ml。使用高效液相色谱(HPLC)对样品进行化学指纹图谱分析,揭示了受试物种之间的一些植物化学相似性和显著差异。本研究为蒿属植物的抗血吸虫潜力提供了支持证据,有必要进行更深入的研究,以确定治疗血吸虫病的潜在新型治疗药物。