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熊果酸和地衣酸化合物的抗衰老和抗肺癌作用及分子模拟研究的生物学研究。

Anti-ageing and Anti-lung Carcinoma Effects of Vulpinic Acid and Usnic Acid Compounds and Biological Investigations with Molecular Modeling Study.

机构信息

Southwest Medical University.

Thoracic surgery, Chendu Wenjiang District People's Hospital.

出版信息

J Oleo Sci. 2022;71(2):247-255. doi: 10.5650/jos.ess21276.

Abstract

Disorganization and breakdown of extracellular matrix proteins like fibronectin, collagen, and elastin are key characteristics of skin aging due to the increased activation of important proteolytic enzymes like elastases and collagenase enzymes. Also, inhibition of their enzymatic activities by natural molecules might be a promising factor to prevent extrinsic skin aging. All chemicals were obtained from Sigma-Aldrich unless otherwise stated. The assay employed was based on spectrophotometric methods reported in the literature. The collagenase and elastase inhibition assays of some phenolic compounds were performed according to the previous studies. These compounds showed excellent to good inhibitory activities of vulpinic acid against studied these enzymes with IC50 values of 195.36 µM for collagenase and 25.24 µM for elastase. The molecular docking calculations were conducted to investigate the chemical and biological activity of vulpinic acid and usnic acid against collagenase and elastase. The results indicated that these two compounds can interact with the essential residues of the enzymes and affect their activities. The calculations of binding free energies were also performed to obtain more details about the characteristics and free energies of the ligand-enzyme complexes. Additionally, both compounds exhibited the most potent inhibition in the three lung cancer cells, with an IC50 value of 21-68 µM, indicating that vulpinic acid is more potent than Doxorubicin, which exhibited an IC50 value of 21-29 µM.

摘要

细胞外基质蛋白(如纤维连接蛋白、胶原蛋白和弹性蛋白)的紊乱和崩解是皮肤衰老的主要特征,这是由于重要的蛋白水解酶(如弹性蛋白酶和胶原酶)的活性增加所致。此外,天然分子抑制这些酶的活性可能是预防外在皮肤衰老的一个有希望的因素。除非另有说明,否则所有化学物质均购自 Sigma-Aldrich。所采用的测定法基于文献中报道的分光光度法。根据先前的研究,对一些酚类化合物的胶原酶和弹性蛋白酶抑制作用进行了测定。这些化合物对研究的这些酶显示出极好的抑制活性,对胶原蛋白酶的抑制活性为 195.36 µM,对弹性蛋白酶的抑制活性为 25.24 µM。进行了分子对接计算,以研究 vulpinic 酸和 usnic 酸对胶原蛋白酶和弹性蛋白酶的化学和生物学活性。结果表明,这两种化合物可以与酶的必需残基相互作用并影响其活性。还进行了结合自由能的计算,以获得有关配体-酶复合物的特性和自由能的更多详细信息。此外,这两种化合物在三种肺癌细胞中均表现出最强的抑制作用,IC50 值为 21-68 µM,表明 vulpinic 酸比 doxorubicin 更有效,doxorubicin 的 IC50 值为 21-29 µM。

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