Manisa Celal Bayar University, Medical Faculty, Department of Parasitology, Manisa, Turkey.
Manisa Celal Bayar University, Medical Faculty, Department of Parasitology, Manisa, Turkey.
Parasitol Int. 2024 Dec;103:102950. doi: 10.1016/j.parint.2024.102950. Epub 2024 Aug 15.
The exploration of alternative agents and novel drug candidates for the effective treatment of cutaneous leishmaniasis has garnered significant attention, driven by the high cost, toxic effects, and the emergence of drug resistance associated with current therapeutic options. Plant extracts derived from Semen Cannabis, the seeds of the Cannabis sativa L. (hemp) plant, and Oleum Hyperici, the oily macerate of Hypericum perforatum L. (St. John's Wort) plant, were prepared by using solvents of varying polarity (n-hexane, chloroform, ethanol, and 60% aqueous ethanol). The primary objective of this study was to research in vitro and ex vivo antileishmanial efficacy of Semen Cannabis and Oleum Hyperici plant extracts against Leishmania tropica promastigotes and intracellular amastigotes. The efficacy of plant extracts against promastigotes were assessed using the cell counting by hemocytometer and the CellTiter-Glo assay. Additionally, their impact on infected THP-1 macrophages and the quantity of intracelluler amastigotes were investigated. Cytotoxicity was evaluated in THP-1 macrophages. Among the tested plant extracts, chloroform extract of Oleum Hyperici demonstrated significant antileishmanial activity against promastigotes (SI: 12.6) and intracellular amastigotes (SI: 16.8) of L. tropica without inducing cytotoxic effects and hold promise for further investigation as potential antileishmanial agents.
大麻籽和贯叶连翘油提取物对利什曼原虫的体外和体内抗利什曼活性研究
大麻籽,大麻属(大麻)植物的种子,和贯叶连翘油,贯叶连翘(金丝桃)植物的油性浸膏,通过使用不同极性的溶剂(正己烷、氯仿、乙醇和 60%的乙醇水溶液)来制备。本研究的主要目的是研究大麻籽和贯叶连翘油植物提取物对利什曼原虫热带前鞭毛体和细胞内无鞭毛体的体外和体内抗利什曼活性。使用血球计数器和 CellTiter-Glo 测定法评估植物提取物对前鞭毛体的疗效。此外,还研究了它们对感染的 THP-1 巨噬细胞和细胞内无鞭毛体数量的影响。在 THP-1 巨噬细胞中评估了细胞毒性。在测试的植物提取物中,贯叶连翘油的氯仿提取物对利什曼原虫热带前鞭毛体(SI:12.6)和细胞内无鞭毛体(SI:16.8)表现出显著的抗利什曼活性,而没有诱导细胞毒性作用,有望进一步研究作为潜在的抗利什曼药物。