Perovskia大麻素Kar萜类部分的治疗作用。动物模型中人畜共患皮肤利什曼病的研究

Q3 Health Professions
Masoud Sadeghi Dinani, J. Rezapour, S. Soleimanifard
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引用次数: 0

摘要

利什曼病是热带国家的一种传染病,可分为皮肤病、粘膜皮肤病和内脏病。由于抗利什曼病药物的副作用、成本和有效性,已经对植物性物质对抗利什曼原虫病的重要性进行了许多临床试验。因此,进行以下研究以评估Perovskia大麻素Kar的治疗效果。萜类成分对Balb/c小鼠皮肤利什曼病的影响。植物花的乙醇∶水(80:20)提取物通过中压液相色谱法使用RP-18柱进行分级。通过TLC和HNMR分析检测富含萜类物质的组分,并评估浓度为0.8%、1.6%和3.2µg/mL对小鼠皮肤利什曼病的治疗效果。使用ANOVA统计检验来评估其效果。结果表明,3.2%浓度的大麻素萜类化合物对治疗小鼠皮肤利什曼病有效,还延长了感染小鼠的寿命并降低了寄生虫负担。根据这一结果,建议将该提取物治疗皮肤利什曼病的有效性作为人体临床试验进行评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment Role of Terpenoid Fraction of Perovskia abrotanoides Kar. on Zoonotic Cutaneous Leishmaniasis in Animal Model
Leishmaniasis is one of the infectious diseases in tropical countries that is seen as cutaneous, mucocutaneous and visceral forms. Due to the side effects, costs and effectiveness of anti-leishmaniasis drugs, many clinical trials have been conducted on the importance of plant-based substances against leishmaniasis. Therefore, the following study was performed to evaluate the therapeutic effects of Perovskia abrotanoides Kar. terpenoid fraction on cutaneous leishmaniasis in Balb/c mice. The ethanol: water (80:20) extract of the plant flowers was fractionated by Medium Pressure Liquid Chromatography using RP-18 column. The terpenoid-rich fraction was detected by TLC and HNMR analyses and evaluated for healing effects on cutaneous leishmaniasis in mice with concentrations of 0.8%, 1.6% and 3.2 µg/mL. The effect of that was evaluated using ANOVA statistical tests. The results indicate that terpenoid of P. abrotanoides in 3.2% concentration is effective in treating cutaneous leishmaniasis in mice and also increases the lifespan and decreases the parasite burden of infected mice. According to this result, it is suggested that the effectiveness of this extract on the treatment of cutaneous leishmaniasis to be evaluated as a clinical trial in humans.
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来源期刊
Traditional and Integrative Medicine
Traditional and Integrative Medicine Health Professions-Complementary and Manual Therapy
CiteScore
1.10
自引率
0.00%
发文量
48
审稿时长
12 weeks
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