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来自[具体来源未提及]的萘醌通过Sirt3调节促进皮肤伤口愈合。

Naphthoquinones from promote skin wound healing through Sirt3 regulation.

作者信息

Ahmad Fayyaz, Bibi Shaheen, Kang Mincheol, Anees Mariam, Ansar Muhammad, Alam Muhammad Rizwan, Kim Sun Yeou, Wahedi Hussain Mustatab

机构信息

Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, 45320 Islamabad, Pakistan.

College of Pharmacy, Gachon University, 191 Hambakmaero, Incheon, South Korea.

出版信息

Iran J Basic Med Sci. 2020 Sep;23(9):1139-1145. doi: 10.22038/ijbms.2020.43706.10275.

Abstract

OBJECTIVES

Lapachone is a natural naphthoquinone-derived compound found in . It is well-known for its analgesic, anti-inflammatory, anti-microbial, diuretic, and anti-cancerous effects. However, the wound-healing effects of this compound are not known yet. The aim of this study was to investigate the wound healing activity of naphthoquinones (α-lapachone and β-lapachone) from .

MATERIALS AND METHODS

Expression of Sirt3, migration-related proteins (Rac1, Cdc42, α-Pak) and angiogenesis-related protein of vascular endothelial growth factor (VEGF) was monitored using western blot analysis. Blood vessel formation and tissue development were monitored by angiogenesis assay and hematoxylin & eosin (H & E) staining, respectively on mouse skin tissue samples. Both α-lapachone and β-lapachone increased Sirt3 expression , but only β-lapachone increased Sirt3 expression

RESULTS

Both the compounds accelerated wound healing in cultured skin cells as well as mouse skin; however, β-lapachone was more effective at lower concentrations. Both of the compounds increased the expression of migration-related proteins both and . Similarly, α-lapachone and β-lapachone increased VEGF expression, tissue development and blood vessel formation in mouse skin.

CONCLUSION

These findings indicated that α-lapachone and β-lapachone are novel Sirt3 activators, and Sirt3 has a role in wound healing. Thus, Sirt3 and its regulators come out as a novel target and potential drug candidates, respectively in the important field of cutaneous wound healing.

摘要

目的

拉帕醇是一种天然萘醌衍生化合物。它以其镇痛、抗炎、抗菌、利尿和抗癌作用而闻名。然而,这种化合物的伤口愈合作用尚不清楚。本研究的目的是研究从[具体来源未给出]中提取的萘醌(α-拉帕醇和β-拉帕醇)的伤口愈合活性。

材料与方法

使用蛋白质免疫印迹分析监测Sirt3、迁移相关蛋白(Rac1、Cdc42、α-Pak)和血管内皮生长因子(VEGF)的血管生成相关蛋白的表达。分别通过血管生成测定和苏木精与伊红(H&E)染色对小鼠皮肤组织样本监测血管形成和组织发育。α-拉帕醇和β-拉帕醇均增加Sirt3表达[此处表述不完整,原文可能有误],但只有β-拉帕醇增加Sirt3表达[此处表述不完整,原文可能有误]

结果

两种化合物在培养的皮肤细胞以及小鼠皮肤中均加速伤口愈合;然而,β-拉帕醇在较低浓度下更有效。两种化合物均增加[此处表述不完整,原文可能有误]迁移相关蛋白的表达。同样,α-拉帕醇和β-拉帕醇增加小鼠皮肤中VEGF表达、组织发育和血管形成。

结论

这些发现表明α-拉帕醇和β-拉帕醇是新型Sirt3激活剂,且Sirt3在伤口愈合中起作用。因此,在皮肤伤口愈合这一重要领域,Sirt3及其调节剂分别成为新的靶点和潜在的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d07e/7491501/396f742d4b6b/IJBMS-23-1139-g001.jpg

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