Plant phenolics inhibit neutrophil elastase

被引:38
作者
Hrenn, Andrea
Steinbrecher, Thomas
Labahn, Andreas
Schwager, Joseph
Schempp, Christoph M.
Merfort, Irmgard
机构
[1] Univ Freiburg, Inst Pharmaceut Sci, Dept Pharmaceut Biol & Biotechnol, D-79104 Freiburg, Germany
[2] Univ Freiburg, Inst Phys Chem, Freiburg, Germany
[3] DSM Nutrit Prod, Kaiseraugst, Switzerland
[4] Univ Freiburg, Dept Dermatol, Freiburg, Germany
关键词
human neutrophil elastase; proliferation; phenolics; genistein; tannins; agrimoniin; resveratrol; ligand docking;
D O I
10.1055/s-2006-946700
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Human neutrophil elastase (HNE) is a serine protease, which is present in its active form in inflamed tissue as well as in psoriatic lesions. In extension of our research on natural compounds as inhibitors of HNE or of its release, several phenolics of different size were tested. The ellagitannins agrimoniin and pedunculagin were the most potent direct HNE inhibitors (IC50 = 0.9 and 2.8 mu M, respectively). Ligand docking calculations provided evidence that inhibition may occur in an unspecific manner. Agrimoniin also showed anti-proliferative effects in the ATP assay (IC50 = 3.2 mu M), suggesting that this type of tannin could have beneficial effects in the treatment of diseases such as psoriasis. Tests with other phenolics combined with ligand docking experiments revealed that, besides the presence of ortho-dihydroxy groups, a specific lipophilic shape is necessary for an inhibitory activity. The phenolic genistein deserves special interest as an inhibitor of elastase release because its effect was remarkably potent (IC50 = 0.6 mu M).
引用
收藏
页码:1127 / 1131
页数:5
相关论文
共 29 条
[1]  
Bos MA, 1996, BIOL PHARM BULL, V19, P146, DOI 10.1248/bpb.19.146
[2]   NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE [J].
BOUKAMP, P ;
PETRUSSEVSKA, RT ;
BREITKREUTZ, D ;
HORNUNG, J ;
MARKHAM, A ;
FUSENIG, NE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :761-771
[3]   THE USE OF ATP BIOLUMINESCENCE AS A MEASURE OF CELL-PROLIFERATION AND CYTOTOXICITY [J].
CROUCH, SPM ;
KOZLOWSKI, R ;
SLATER, KJ ;
FLETCHER, J .
JOURNAL OF IMMUNOLOGICAL METHODS, 1993, 160 (01) :81-88
[4]   Pharmacokinetics of the green tea derivative, EGCG, by the topical route of administration in mouse and human skin [J].
Dvorakova, K ;
Dorr, RT ;
Valcic, S ;
Timmermann, B ;
Alberts, DS .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1999, 43 (04) :331-335
[5]  
GEIGER C, 1990, Planta Medica, V56, P585, DOI 10.1055/s-2006-961192
[6]   PROANTHOCYANIDINS WITH (+)-EPICATECHIN UNITS FROM BYRSONIMA-CRASSIFOLIA BARK [J].
GEISS, F ;
HEINRICH, M ;
HUNKLER, D ;
RIMPLER, H .
PHYTOCHEMISTRY, 1995, 39 (03) :635-643
[7]  
Kramer B, 1999, PROTEINS, V37, P228, DOI 10.1002/(SICI)1097-0134(19991101)37:2<228::AID-PROT8>3.0.CO
[8]  
2-8
[9]  
Melzig MF, 2001, PHARMAZIE, V56, P967
[10]  
Melzig MF, 1999, PHARMAZIE, V54, P712