Collagenase and Tyrosinase Inhibitory Effect of Isolated Constituents from the Moss Polytrichum formosum

被引:11
作者
Marques, Raissa Volpatto [1 ]
Guillaumin, Agnes [2 ]
Abdelwahab, Ahmed B. [2 ]
Salwinski, Aleksander [2 ]
Gotfredsen, Charlotte H. [3 ]
Bourgaud, Frederic [2 ,4 ]
Enemark-Rasmussen, Kasper [3 ]
Miguel, Sissi [4 ]
Simonsen, Henrik Toft [1 ]
机构
[1] Tech Univ Denmark, Dept Biotechnol & Biomed, Soltoft Plads 223, DK-2800 Lyngby, Denmark
[2] Plant Adv Technol, 19 Ave Foret Haye, F-54500 Vandoeuvre Les Nancy, France
[3] Tech Univ Denmark, Dept Chem, Kemitorvet 207, DK-2800 Lyngby, Denmark
[4] Cellengo, 19 Ave Foret Haye, F-54500 Vandoeuvre Les Nancy, France
来源
PLANTS-BASEL | 2021年 / 10卷 / 07期
基金
欧盟地平线“2020”;
关键词
Polytrichum formosum; Polytrichaceae; mosses; bryophytes; benzonaphthoxanthenones; ohioensins; collagenase inhibitory activity; tyrosinase inhibitory activity; HUMAN FIBROBLAST COLLAGENASE; OHIOENSIN-F; BENZONAPHTHOXANTHENONES; EXPRESSION; DOCKING;
D O I
10.3390/plants10071271
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Mosses from the genus Polytrichum have been shown to contain rare benzonaphthoxanthenones compounds, and many of these have been reported to have important biological activities. In this study, extracts from Polytrichum formosum were analyzed in vitro for their inhibitory properties on collagenase and tyrosinase activity, two important cosmetic target enzymes involved respectively in skin aging and pigmentation. The 70% ethanol extract showed a dose-dependent inhibitory effect against collagenase (IC50 = 4.65 mg/mL). The methanol extract showed a mild inhibitory effect of 44% against tyrosinase at 5.33 mg/mL. Both extracts were investigated to find the constituents having a specific affinity to the enzyme targets collagenase and tyrosinase. The known compounds ohioensin A (1), ohioensin C (3), and communin B (4), together with nor-ohioensin D (2), a new benzonaphthoxanthenone, were isolated from P. formosum. Their structures were determined by mass spectrometry and NMR spectroscopy. Compounds 1 (IC50 = 71.99 mu M) and 2 (IC50 = 167.33 mu M) showed inhibitory activity against collagenase. Compound 1 also exhibited inhibition of 30% against tyrosinase activity at 200 mu M. The binding mode of the active compounds was theoretically generated by an in-silico approach against the 3D structures of collagenase and tyrosinase. These current results present the potential application from the moss P. formosum as a new natural source of collagenase and tyrosinase inhibitors.
引用
收藏
页数:13
相关论文
共 34 条
[1]   Matrix Metalloproteinases: How Much Can They Do? [J].
Agren, Magnus S. ;
auf dem Keller, Ulrich .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (08)
[2]  
Akinori H., 2003, JP Patent, Patent No. [2003321376A, 2003321376]
[3]   Matrix metalloproteinase collagenolysis in health and disease [J].
Amar, Sabrina ;
Smith, Lyndsay ;
Fields, Gregg B. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2017, 1864 (11) :1940-1951
[4]   Biologically active compounds from bryophytes [J].
Asakawa, Yoshinori .
PURE AND APPLIED CHEMISTRY, 2007, 79 (04) :557-580
[5]  
AULD DS, 1995, METHOD ENZYMOL, V248, P228
[6]   Collagen: A review on its sources and potential cosmetic applications [J].
Avila Rodriguez, Maria Isabela ;
Rodriguez Barroso, Laura G. ;
Lorena Sanchez, Mirna .
JOURNAL OF COSMETIC DERMATOLOGY, 2018, 17 (01) :20-26
[7]   Tyrosinase: A Central Regulatory Protein for Cutaneous Pigmentation [J].
Bae-Harboe, Yoon-Soo Cindy ;
Park, Hee-Young .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2012, 132 (12) :2678-2680
[8]  
Bhattarai HD, 2009, Z NATURFORSCH C, V64, P197
[9]   Ohioensin F suppresses TNF-α-induced adhesion molecule expression by inactivation of the MAPK, Akt and NF-κB pathways in vascular smooth muscle cells [J].
Byeon, Hye-Eun ;
Um, Sung Hee ;
Yim, Joung Han ;
Lee, Hong Kum ;
Pyo, Suhkneung .
LIFE SCIENCES, 2012, 90 (11-12) :396-406
[10]   Plant Milking Technology-An Innovative and Sustainable Process to Produce Highly Active Extracts from Plant Roots [J].
Chajra, Hanane ;
Salwinski, Aleksander ;
Guillaumin, Agnes ;
Mignard, Benoit ;
Hannewald, Paul ;
Duriot, Leonor ;
Warnault, Pierre ;
Guillet-Claude, Carine ;
Frechet, Mathilde ;
Bourgaud, Frederic .
MOLECULES, 2020, 25 (18)