Extracts from European Propolises as Potent Tyrosinase Inhibitors

被引:8
|
作者
Widelski, Jaroslaw [1 ]
Gawel-Beben, Katarzyna [2 ]
Czech, Karolina [2 ]
Paluch, Emil [3 ]
Bortkiewicz, Olga [3 ]
Kozachok, Solomiia [4 ]
Mroczek, Tomasz [5 ]
Okinczyc, Piotr [6 ]
机构
[1] Med Univ Lublin, Dept Pharmacognosy Med Plants Garden, ul Chodzki 1 Collegium Unive, PL-20093 Lublin, Poland
[2] Univ Informat Technol & Management Rzeszow, Dept Cosmetol, 2 Sucharskiego, PL-35225 Rzeszow, Poland
[3] Wroclaw Med Univ, Fac Med, Dept Microbiol, Tytusa Chalubinskiego 4, PL-50376 Wroclaw, Poland
[4] Inst Soil Sci & Plant Cultivat, State Res Inst, Dept Biochem & Crop Qual, Czartoryskich 8, PL-24100 Pulawy, Poland
[5] Med Univ Lublin, Dept Nat Prod Chem, PL-20093 Lublin, Poland
[6] Wroclaw Med Univ, Dept Pharmacognosy & Herbal Med, Borowska 211a, PL-50556 Wroclaw, Poland
来源
MOLECULES | 2023年 / 28卷 / 01期
关键词
propolis; tyrosinase; inhibitor; UHPLC-DAD-MS; MS; antioxidant; melanin; monophenolase; diphenolase; phenolic acid glycerides; galangin; chrysin; PERSPECTIVE; FLAVONOIDS;
D O I
10.3390/molecules28010055
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tyrosinase is a key enzyme in the melanogenesis pathway. Melanin, the product of this process, is the main pigment of the human skin and a major protection factor against harmful ultraviolet radiation (UVR). Increased melanin synthesis due to tyrosinase hyperactivity can cause hyperpigmentation disorders, which in consequence causes freckles, age spots, melasma, or postinflammatory hyperpigmentation. Tyrosinase overproduction and hyperactivity are triggered by the ageing processes and skin inflammation as a result of oxidative stress. Therefore, the control of tyrosinase activity is the main goal of the prevention and treatment of pigmentation disorders. Natural products, especially propolis, according to their phytochemical profile abundant in polyphenols, is a very rich resource of new potential tyrosinase inhibitors. Therefore, this study focused on the assessment of the tyrosinase inhibitory potential of six extracts obtained from the European propolis samples of various origins. The results showed the potent inhibitory activity of all tested propolis extracts towards commercially available mushroom tyrosinase. The four most active propolis extracts showed inhibitory activity in the range of 86.66-93.25%. Apart from the evaluation of the tyrosinase inhibition, the performed research included UHPLC-DAD-MS/MS (ultra high performance liquid chromatography coupled with diode array detection and tandem mass spectrometry) phytochemical profiling as well as antioxidant activity assessment using the 2,2-diphenyl-1-picrylhydrazyl (DPPH) and the 2,2"-azino-bis(3-ethylbenzothiazoline-6-sulfuric acid (ABTS) radical scavenging tests. Moreover, statistical analysis was used to correlate the tyrosinase inhibitory and antioxidant activities of propolis extracts with their phytochemical composition. To summarise, the results of our research showed that tested propolis extracts could be used for skin cosmeceutical and medical applications.
引用
收藏
页数:11
相关论文
共 50 条
  • [21] Umbelliferone-Thiazolidinedione Hybrids as Potent Mushroom Tyrosinase Inhibitors
    Molnar, Maja
    Kovac, Tihomir
    Strelec, Ivica
    INTERNATIONAL JOURNAL OF PHARMACEUTICAL RESEARCH AND ALLIED SCIENCES, 2016, 5 (02): : 305 - 310
  • [22] Insights into the Explication of Potent Tyrosinase Inhibitors with Reference to Computational Studies
    Parveen, Naima
    Ali, Sharique Akhtar
    Ali, Ayesha Sharique
    LETTERS IN DRUG DESIGN & DISCOVERY, 2019, 16 (11) : 1182 - 1193
  • [23] Chalcones as potent tyrosinase inhibitors: the effect of hydroxyl positions and numbers
    Nerya, O
    Musa, R
    Khatib, S
    Tamir, S
    Vaya, J
    PHYTOCHEMISTRY, 2004, 65 (10) : 1389 - 1395
  • [24] N-benzylbenzamides: A new class of potent tyrosinase inhibitors
    Cho, SJ
    Roh, JS
    Sun, WS
    Kim, SH
    Park, KD
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2006, 16 (10) : 2682 - 2684
  • [25] Novel morpholine containing cinnamoyl amides as potent tyrosinase inhibitors
    Ghafary, Shahrzad
    Ranjbar, Sara
    Larijani, Bagher
    Amini, Mohsen
    Biglar, Mahmood
    Mahdavi, Mohammad
    Bakhshaei, Maryam
    Khoshneviszadeh, Mahsima
    Sakhteman, Amirhossein
    Khoshneviszadeh, Mehdi
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2019, 135 : 978 - 985
  • [26] Molecular design of potent tyrosinase inhibitors having the bibenzyl skeleton
    Oozeki, Hiromi
    Tajima, Reiko
    Nihei, Ken-ichi
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (19) : 5252 - 5254
  • [27] Diarylpropanes as a novel class of potent tyrosinase inhibitors and their biological properties
    Jia, Q.
    Zhao, J.
    Hong, M.
    Zhao, Y.
    Yimam, M.
    O'Reilly, T.
    Ma, W.
    Padmapriya, A.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2007, 127 : S151 - S151
  • [28] Tyrosinase inhibitors from plants
    Kubo, I
    PHYTOCHEMICALS FOR PEST CONTROL, 1997, 658 : 311 - 326
  • [29] Tyrosinase inhibitors from cumin
    Kubo, I
    Kinst-Hori, I
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1998, 46 (12) : 5338 - 5341
  • [30] N-[(Dihydroxyphenyl)acyl]serotonins as potent inhibitors of tyrosinase from mouse and human melanoma cells
    Yamazaki, Yoshimitsu
    Kawano, Yasuhiro
    Yamanaka, Akiko
    Maruyama, Susumu
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2009, 19 (15) : 4178 - 4182