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通过体内、体外和计算机模拟分析对烟曲霉进行生物学研究。

Biological investigations of Aspergillus ficuum via in vivo, in vitro and in silico analyses.

作者信息

Shah Zafar Ali, Khan Khalid, Shah Tanzeel, Ahmad Nasir, Muhammad Akhtar, Rashid Haroon Ur

机构信息

Department of Chemistry, Islamia College University, Peshawar, Khyber Pakhtunkhwa, Pakistan.

Institute of Basic Medical Sciences, Khyber Medical University, Peshawar, Khyber Pakhtunkhwa, Pakistan.

出版信息

Sci Rep. 2023 Oct 11;13(1):17260. doi: 10.1038/s41598-023-43819-y.

Abstract

Serious human health impacts have been observed worldwide due to several life-threatening diseases such as cancer, candidiasis, hepatic coma, and gastritis etc. Exploration of nature for the treatment of such fatal diseases is an area of immense interest for the scientific community. Based on this idea, the genus Aspergillus was selected to discover its hidden therapeutic potential. The genus Aspergillus is known to possess several biologically active compounds. The current research aimed to assess the biological and pharmacological potency of the extracts of less-studied Aspergillus ficuum (FCBP-DNA-1266) (A. ficuum) employing experimental and bioinformatics approaches. The disc diffusion method was used for the antifungal investigation, and the MTT assay was performed to assess the anticancer effects. Mice were employed as an in vivo model to evaluate the antispasmodic effects. A standard spectrophotometric technique was applied to gauge the urease inhibitory activity. The antifungal studies indicate that both n-hexane and ethyl acetate extracts were significantly active against Candida albicans (C. albicans) with their zone of inhibitions (ZOI) values reported as 19 ± 1.06 mm and 25 ± 0.55 mm, respectively at a dose of 30 µg.mL. In vitro cytotoxicity assay against HeLa, fibroblast 3T3, prostate PC3, and breast MCF-7 cancer cell lines was performed. The ethyl acetate extract of A. ficuum was found to be significantly active against MCF-7 with its IC value of 43.88 µg.mL. However, no substantial effects on the percent cell death of HeLa cancer cell lines were observed. In addition, the A. ficuum extracts also inhibited the urease enzyme compared to standard thiourea. The antispasmodic activity of A. ficuum extract was assessed by an in vivo model and the results demonstrated promising activity at 150 mg.kg. Molecular docking results also supported the antifungal, anticancer, and antiurease potency of A. ficuum extract. Overall, the results display promising aspects of A. ficuum extract as a future pharmacological source.

摘要

由于癌症、念珠菌病、肝昏迷和胃炎等几种危及生命的疾病,在全球范围内已观察到对人类健康的严重影响。探索自然界以治疗此类致命疾病是科学界极为感兴趣的领域。基于这一想法,选择了曲霉属来发现其潜在的治疗潜力。已知曲霉属拥有多种生物活性化合物。当前的研究旨在采用实验和生物信息学方法评估研究较少的烟曲霉(FCBP-DNA-1266)(烟曲霉)提取物的生物学和药理活性。采用纸片扩散法进行抗真菌研究,并进行MTT试验以评估抗癌效果。使用小鼠作为体内模型来评估解痉作用。应用标准分光光度技术来测定脲酶抑制活性。抗真菌研究表明,正己烷和乙酸乙酯提取物对白色念珠菌均具有显著活性,在30μg.mL的剂量下,其抑菌圈(ZOI)值分别报告为19±1.06mm和25±0.55mm。对人宫颈癌HeLa细胞、成纤维细胞3T3、前列腺癌PC3细胞和乳腺癌MCF-7细胞系进行了体外细胞毒性试验。发现烟曲霉的乙酸乙酯提取物对MCF-7具有显著活性,其IC值为43.88μg.mL。然而,未观察到对HeLa癌细胞系细胞死亡百分比有实质性影响。此外,与标准硫脲相比,烟曲霉提取物也能抑制脲酶。通过体内模型评估了烟曲霉提取物的解痉活性,结果表明在150mg.kg时具有良好的活性。分子对接结果也支持了烟曲霉提取物的抗真菌、抗癌和抗脲酶活性。总体而言,结果显示烟曲霉提取物作为未来的药理学来源具有良好的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d7f/10570320/3f96ca55aacf/41598_2023_43819_Fig1_HTML.jpg

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