Department of Pharmacognosy and Biomaterials, Poznan University of Medical Sciences, Rokietnicka 3 Str., 60-806 Poznań, Poland.
Department of Biotechnology, Microbiology and Human Nutrition, University of Life Sciences in Lublin, Skromna 8 Str., 20-704 Lublin, Poland.
Molecules. 2023 Dec 31;29(1):233. doi: 10.3390/molecules29010233.
is a lichen widely distributed in the Northern Hemisphere. Its biological properties still need to be discovered. Therefore, our paper focuses on studies of extracts, including its main metabolites evernic acid (EA) or atranorin (ATR). Phytochemical profiles using chromatographic analysis were confirmed. The antioxidant activity was evaluated using in vitro chemical tests and in vitro enzymatic cells-free tests, namely superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione reductase (GR), and catalase (CAT). The anti-inflammatory potential using cyclooxygenase-2 (COX-2) and hyaluronidase were determined. The neuroprotective potential using acetylcholinesterase, (AChE), butyrylcholinesterase (BChE), and tyrosinase (Tyr) was estimated. The hypoglycemic activity was also confirmed (α-glucosidase). Principal component analysis was performed to determine the relationship between the biological activity of extracts. The inhibitory effect of EA and ATR on COX-2 AChE, BChE, Tyr, and α-glucosidase was evaluated using molecular docking techniques and confirmed for EA and ATR (besides α-glucosidase). The penetration of EA and ATR from extracts through the blood-brain barrier was confirmed using the parallel artificial membrane permeability assay blood-brain barrier test. In conclusion, depending on chemical surroundings and the concentration, the extracts, EA or ATR, showed attractive pleiotropic properties, which should be further investigated.
是一种广泛分布于北半球的地衣。其生物特性尚待发现。因此,我们的论文侧重于 提取物的研究,包括其主要代谢物evernic 酸(EA)或atranaorin(ATR)。使用色谱分析确认了植物化学特征。使用体外化学测试和体外无细胞酶测试,即超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)、谷胱甘肽还原酶(GR)和过氧化氢酶(CAT),评估了抗氧化活性。通过环加氧酶-2(COX-2)和透明质酸酶测定了抗炎潜力。使用乙酰胆碱酯酶(AChE)、丁酰胆碱酯酶(BChE)和酪氨酸酶(Tyr)估计了神经保护潜力。还证实了降血糖活性(α-葡萄糖苷酶)。进行了主成分分析,以确定提取物的生物活性之间的关系。使用分子对接技术评估了 EA 和 ATR 对 COX-2、AChE、BChE、Tyr 和α-葡萄糖苷酶的抑制作用,并对 EA 和 ATR 进行了确认(除了α-葡萄糖苷酶)。使用平行人工膜渗透测定法血脑屏障试验证实了 EA 和 ATR 从提取物穿过血脑屏障的渗透。总之,取决于化学环境和浓度, 提取物、EA 或 ATR 表现出有吸引力的多效性,应进一步研究。