从内生真菌Phomopsis sp CAM212中分离的三种天然聚酮对痢疾致病菌的抗炎和抗菌作用

Marie Louise Medoua, Sylvain Nsangou Pechangou, B. E. Enang II, Assam Assam Jean Paul, E. Njoya, F. N. Njayou, P. Moundipa
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引用次数: 0

摘要

目的:评价三种天然多酮类化合物CAM212的抗阿米巴、抗菌和抗炎活性。研究设计:采用临床分离的溶组织芽胞杆菌、大肠杆菌ATCC25922株、原代小鼠腹腔巨噬细胞和三种聚酮。学习地点和时间:2022年5月至12月,雅温得第一大学理学院药理学和毒理学实验室,医学微生物实验室。方法:在这项工作中,我们评估了三种天然多酮从磷藓sp抑制细菌的生长负责阿米巴和细菌性痢疾的能力。首先,对临床分离的溶组织芽胞杆菌进行了多种培养的抗阿米巴活性研究。随后,我们评估了大肠杆菌ATCC25922菌株的抗菌潜力。最后,通过抑制一氧化氮(NO)的产生、磷酸酶碱性(ALP)的激活和5-脂氧合酶(5-LOX)的抑制,在SC活化的巨噬细胞原代培养中评估其抗炎能力。结果:phomopsinin B对阿米巴的抑制作用最强(72h后抑制率为84.4%),抑菌作用最强(MIC=12.5µg/mL, MBC/MIC=2)。麻藻A和醋酸麻藻A表现出中等的抗阿米巴和抗菌潜能。但这些活性均低于甲硝唑和环丙沙星(72h后阿米巴抑制率为90%;MIC=0.72µg/mL, MBC/MIC=4)。随后,所有测试的化合物对原代巨噬细胞无毒。Phomopsinin B通过抑制NO生成显示出很强的抗炎潜能(IC50=1.72±0.91µg/mL);抑制5-LOX活性(IC50=36.97±7.12µg/mL)和ALP活性(IC50=0.13±0.01µg/mL)。与黄芩苷相比,青蒿素A和青蒿素A醋酸酯具有较低的抗炎潜能。结论:在所测化合物中,phomopsinin B的抗阿米巴、抗菌和抗炎潜能在试验范围内均达到各自标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-inflammatory and Antimicrobial Potential of Three Natural Polyketides Isolated from Endophytic Fungus Phomopsis sp CAM212 against to Dysenteric Causing Pathogens
Aims: The present work aimed to evaluate the anti-amoebic, antibacterial, and anti-inflammatory potential of three natural polyketides from Phomopsis sp. CAM212. Study Design: Clinical isolates of E.histolytica, E.coli ATCC25922 strain, primary peritoneal mouse macrophages and three polyketides were used. Places and Duration of Study: Laboratory of Pharmacology and Toxicology, Laboratory of Medical Microbiology, Faculty of Science, University of Yaounde 1 between May and December 2022. Methodology: During this work, we evaluated the ability of three natural polyketides from Phomopsis sp to inhibit the growth of germs responsible for amoebic and bacillary dysentery. First, the anti-amoebic activity was carried out on clinical isolates of E. histolytica in polyxenic culture. Subsequently, we evaluated the antibacterial potential on a strain of E. coli ATCC25922. Finally, the anti-inflammatory potentials were evaluated on a primary culture of SC activated macrophages through inhibition of nitric oxide (NO) production, activation of phosphatase alcaline (ALP) and inhibition of 5-lipoxygenase (5-LOX). Results: It emerges from this work that among compounds, phomopsinin B, presented the highest anti-amoebic potential (84.4 % inhibition after 72h) and the highest antibacterial potential (MIC=12.5µg/mL and MBC/MIC=2). Phomopsini A and phomopsini A acetate showed moderate anti amoebic and antibacterial potentials. However, all these activities remain lower than that of metronidazole and ciprofloxacin (90% of amoebic inhibition after 72h; MIC=0.72µg/mL and MBC/MIC=4). Subsequently, all tested compounds were nontoxic on primary macrophages. Phomopsinin B exhibited a great anti-inflammatory potential through the inhibition of NO production (IC50=1.72±0.91µg/mL); inihibition of 5-LOX activity (IC50=36.97±7.12µg/mL) and activation of ALP activity (IC50=0.13±0.01µg/mL) as compared to Baicalin the standard. The anti-inflammatory potential of phomopsinin A and phomopsinin A acetate were lower compared to baicalin. Conclusion: Ultimately, among compounds tested, phomopsinin B exhibited the best anti-amoebic, antibacterial and ant-inflammatory potential similar to the respective standards within the limits of the tests carried out.
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