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

被引:2
作者
Shah, Zafar Ali [1 ]
Khan, Khalid [1 ]
Shah, Tanzeel [2 ]
Ahmad, Nasir [1 ]
Muhammad, Akhtar [1 ]
Rashid, Haroon Ur [3 ,4 ]
机构
[1] Islamia Coll Univ, Dept Chem, Peshawar, Khyber Pakhtunk, Pakistan
[2] Khyber Med Univ, Inst Basic Med Sci, Peshawar, Khyber Pakhtunk, Pakistan
[3] Univ Fed Pelotas, Ctr Chem Pharmaceut & Food Sci, Pelotas, RS, Brazil
[4] Sao Paulo State Univ, Inst Chem, Araraquara, SP, Brazil
关键词
INHIBITION; ANTICANCER; UREASE;
D O I
10.1038/s41598-023-43819-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 mu g.mL(-1). 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 IC50 value of 43.88 mu g.mL(-1). 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(-1). 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.
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页数:13
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共 48 条
[1]   Structural Analysis of the Mechanism of Inhibition and Allosteric Activation of the Kinase Domain of HER2 Protein [J].
Aertgeerts, Kathleen ;
Skene, Robert ;
Yano, Jason ;
Sang, Bi-Ching ;
Zou, Hua ;
Snell, Gyorgy ;
Jennings, Andy ;
Iwamoto, Keiji ;
Habuka, Noriyuki ;
Hirokawa, Aki ;
Ishikawa, Tomoyasu ;
Tanaka, Toshimasa ;
Miki, Hiroshi ;
Ohta, Yoshikazu ;
Sogabe, Satoshi .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (21) :18756-18765
[2]  
[Anonymous], 2012, Molecular Operating Environment (MOE), V10
[3]  
[Anonymous], 2011, The Gulf of Mexico at a Glance: A Second Glance, P1, DOI DOI 10.17226/12910
[4]   Paecilomyces formosus MD12, a Biocontrol Agent to Treat Meloidogyne incognita on Brinjal in Green House [J].
Baazeem, Alaa ;
Alorabi, Mohammed ;
Manikandan, Palanisamy ;
Alotaibi, Saqer S. ;
Almanea, Abdulaziz ;
Abdel-Hadi, Ahmed ;
Vijayaraghavan, Ponnuswamy ;
Raj, Subhanandharaj Russalamma Flanet ;
Kim, Young Ock ;
Kim, Hak-Jae .
JOURNAL OF FUNGI, 2021, 7 (08)
[5]   Crystal Structure of the First Plant Urease from Jack Bean: 83 Years of Journey from Its First Crystal to Molecular Structure [J].
Balasubramanian, Anuradha ;
Ponnuraj, Karthe .
JOURNAL OF MOLECULAR BIOLOGY, 2010, 400 (03) :274-283
[6]   In silico detection of potential inhibitors from vitamins and their derivatives compounds against SARS-CoV-2 main protease by using molecular docking, molecular dynamic simulation and ADMET profiling [J].
Belhassan, Assia ;
Chtita, Samir ;
Zaki, Hanane ;
Alaqarbeh, Marwa ;
Alsakhen, Nada ;
Almohtaseb, Firas ;
Lakhlifi, Tahar ;
Bouachrine, Mohammed .
JOURNAL OF MOLECULAR STRUCTURE, 2022, 1258
[7]   Endophytic fungus Paecilomyces formosus LHL10 produces sester-terpenoid YW3548 and cyclic peptide that inhibit urease and α-glucosidase enzyme activities [J].
Bilal, Saqib ;
Ali, Liaqat ;
Khan, Abdul Latif ;
Shahzad, Raheem ;
Asaf, Sajjad ;
Imran, Muhammad ;
Kang, Sang-Mo ;
Kim, Sang-Kuk ;
Lee, In-Jung .
ARCHIVES OF MICROBIOLOGY, 2018, 200 (10) :1493-1502
[8]   Anticancer and Antifungal Compounds from Aspergillus, Penicillium and Other Filamentous Fungi [J].
Bladt, Tanja Thorskov ;
Frisvad, Jens Christian ;
Knudsen, Peter Boldsen ;
Larsen, Thomas Ostenfeld .
MOLECULES, 2013, 18 (09) :11338-11376
[9]   Yanuthones:: Novel metabolites from a marine isolate of Aspergillus niger [J].
Bugni, TS ;
Abbanat, D ;
Bernan, VS ;
Maiese, WM ;
Greenstein, M ;
Van Wagoner, RM ;
Ireland, CM .
JOURNAL OF ORGANIC CHEMISTRY, 2000, 65 (21) :7195-7200
[10]  
Devi R., 2020, New and Future Developments in Microbial Biotechnology and Bioengineering 1˚edicao, P147, DOI [DOI 10.1016/B978-0-12-820528-0.00010-7, 10.1016/B978-0-12-820528-0.00010-7]