赭石提取物对皮肤利什曼病原生体体外活力的活性与斯地溴酸钠药物的比较

Sanya abdulkareem AL- Qormuti, Noman Alhatemi, Laith Alosoufe, Sala mohammed Al-awj, Almanwar mohammed Alsalahi, Gubran hamid Albukhaiti, Taiseer Abdul-raheem Shamsan, Haneef Hasan Alhogami, M. Al-Fakih, Shaima Taher Al-Shehri, Marwa Mohamad Ibraheim
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引用次数: 0

摘要

本研究调查了用不同溶剂(乙醇、甲醇和蒸馏水)制备的 Argemone ochroleuca 叶植物提取物对皮肤利什曼病原虫体外生存能力的抑制活性,并将其与已确定的药物斯地巴葡萄糖酸钠进行了比较。由利什曼寄生虫引起的皮肤利什曼病对全球健康构成了重大挑战。由利什曼病寄生虫引起的皮肤利什曼病对全球健康构成重大挑战。传统治疗方法,如施替葡糖酸钠,存在毒性和耐药性等局限性。Argemone ochroleuca 植物提取物以乙醇、甲醇和蒸馏水为溶剂进行制备。采用基于时间的方法评估了对原生体活力的抑制作用,测量了抑制作用发生所需的持续时间(以秒为单位)。有趣的是,在某些浓度下,萃取物显示出与斯地巴葡萄糖酸钠相当甚至更强的功效。研究结果与施托葡糖酸钠的抑制效果进行了比较。研究结果表明,Argemone ochroleuca 植物提取物的抑制时间如下:乙醇:当浓度为 400 毫克/毫升时,抑制时间为 9 秒;当浓度为 200 毫克/毫升时,抑制时间为 26 秒;当浓度为 100 毫克/毫升时,抑制时间为 60 秒;当浓度为 50 毫克/毫升时,抑制时间为 128 秒:水生提取物:抑制作用发生在 400 毫克/毫升时为 13 秒,200 毫克/毫升时为 39 秒,100 毫克/毫升时为 91 秒,50 毫克/毫升时为 210 秒;抑制作用发生在 400 毫克/毫升时为 94 秒,200 毫克/毫升时为 150 秒,100 毫克/毫升时为 258 秒,50 毫克/毫升时为 474 秒。这些结果表明,水黄皮树叶植物提取物,尤其是用乙醇和甲醇制备的提取物,对皮肤利什曼病原体的活力有很强的抑制作用。不同溶剂在抑制时间上的差异表明,生物活性化合物的提取和相互作用存在差异。乙醇和甲醇提取物具有更快、更有效的抑制作用,是传统疗法的潜在替代品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Activity of Argemone Ochroleuca Extract On the in Vitro Viability of Cutaneous Leishmaniasis Promastigotes Comparison to Sodium Stibogluconate Drug
This study investigates the inhibitory activity of Argemone ochroleuca leaf plant extracts which was so prepared by using different solvents (ethanol, methanol, and distilled water) on the in vitro viability of cutaneous leishmaniasis promastigotes, in comparison with the established drug sodium stibogluconate.Cutaneous leishmaniasis, caused by Leishmania parasites, poses significant health challenges globally. Conventional treatments, like sodium stibogluconate, have limitations such as toxicity and drug resistance. Plant extracts, owing to their diverse bioactive constituents, present a potential alternative for disease management.Argemone ochroleuca plant extracts were prepared using ethanol, methanol, and distilled water as solvents. The inhibitory effect on promastigote viability was assessed using a time-based approach, measuring the duration in seconds that is required for inhibition to occur. Interestingly, at certain concentrations, the extract exhibited comparable or even superior efficacy to sodium stibogluconate. Results were compared with the inhibitory effect of sodium stibogluconate. The findings demonstrate the following inhibitory times for Argemone ochroleuca plant extracts: Ethanol: Inhibition occurred at 400 mg/ml in 9 seconds, at 200 mg/ml in 26 seconds, at 100 mg/ml in 60 seconds, and at 50 mg/ml in 128 seconds, Methanol: Inhibition occurred at 400 mg/ml in 13 seconds, at 200 mg/ml in 39 seconds, at 100 mg/ml in 91 seconds, and at 50 mg/ml in 210 seconds and Aquatic extract: Inhibition occurred at 400 mg/ml in 94 seconds, at 200 mg/ml in 150 seconds, at 100 mg/ml in 258 seconds, and at 50 mg/ml in 474 seconds. Comparatively, sodium stibogluconate showed its inhibitory effect at a specific concentration 100 mg/ml in 10 second.These results indicate that the Argemone ochroleuca leaves plant extracts, particularly those prepared using ethanol and methanol, exhibit substantial inhibitory effects on the viability of cutaneous leishmaniasis promastigotes. The variations in inhibitory times among the solvents suggest differences in the bioactive compound extraction and interactions. Ethanol and methanol extracts present potential alternatives to conventional treatments, with faster and efficient inhibitory action.Further research is warranted to elucidate the specific bioactive compounds responsible for these inhibitory effects and to explore the underlying.
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