Fakhrieh-Kashan Zohreh, Arbabi Mohsen, Delavari Mahdi, Mohebali Mahdi, Hooshyar Hossein
Dept. of Medical Parasitology and Mycology, School of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Dept. of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Iran J Parasitol. 2018 Jan-Mar;13(1):72-78.
The protozoan is a sexually transmitted disease (STD). Metronidazole is a chosen drug for the treatment. This study evaluated the anti trichomonal activity of alcoholic extracts of combination and
This experimental study was conducted in the Parasitology Laboratory, Kashan University of Medical Sciences, Kashan, Iran in 2015, on 23 women with suspected trichomoniasis referring to Kashan clinical centers. Medium TYI-S-33 was used for culture of three isolates. Different concentrations (25, 50, 100, 200, 400, 800 μg/ml) of and ethanol extract added to trophozoites in 48-well plates and metronidazole considered as positive control and the negative control was TYI-S33 containing trophozoites without any drug. In all of mentioned groups, trophozoites number counted 12, 24, 48 h after culture. Results were analyzed using ANOVA statistical test, to evaluate the toxicity of extract, measured by MTT assay. Induced apoptosis of after treatment with different concentrations of extract was determined by Flow Cytometry.
IC50 of alcoholic extract of combination and and metronidazole after 24h was 73.80 μg/ml and 0.0326 μg/ml, respectively. The toxicity percentage of 25-800 μg/ml concentrations of this combination were between 0.2-1.98. In different concentrations of extract (25,50,100,200 and 400 μg/ml) apoptosis percent after 48h was 18.97 to 77.19 and necrosis percent was calculated 1.35, 3.18, 3.10, 1.16 and 4.09, respectively.
Alcoholic extract of combination and induces programmed death in . Due to no toxicity on macrophages, it can be examined in vivo studies.
原生动物是一种性传播疾病。甲硝唑是治疗该病的常用药物。本研究评估了[组合名称]酒精提取物的抗滴虫活性。
2015年,在伊朗卡尚医科大学寄生虫学实验室对23名疑似滴虫病的女性进行了这项实验研究,这些女性均前往卡尚临床中心就诊。使用TYI-S-33培养基培养三种[滴虫]分离株。将不同浓度(25、50、100、200、400、800μg/ml)的[组合名称]乙醇提取物添加到48孔板中的滋养体中,甲硝唑作为阳性对照,阴性对照为含有滋养体但无任何药物的TYI-S33。在上述所有组中,培养12、24、48小时后对滋养体数量进行计数。使用方差分析统计检验分析结果,通过MTT法测定提取物的毒性。通过流式细胞术测定不同浓度提取物处理后[滴虫]的诱导凋亡情况。
24小时后,[组合名称]酒精提取物和甲硝唑的半数抑制浓度(IC50)分别为73.80μg/ml和0.0326μg/ml。该组合25 - 800μg/ml浓度的毒性百分比在0.2 - 1.98之间。在不同浓度的提取物(25、50、100、200和400μg/ml)中,48小时后的凋亡率为18.97%至77.19%,坏死率分别计算为1.35%、3.18%、3.10%、1.16%和4.09%。
[组合名称]酒精提取物可诱导[滴虫]程序性死亡。由于对巨噬细胞无毒性,可在体内研究中进行检测。