The effect of sesquiterpene lactones on the release of human neutrophil elastase

被引:44
作者
Siedle, B
Gustavsson, L
Johansson, S
Murillo, R
Castro, V
Bohlin, L
Merfort, I
机构
[1] Univ Freiburg, Inst Pharmazeut Biol, D-79104 Freiburg, Germany
[2] Uppsala Univ, Ctr Biomed, Dept Med Chem, Div Pharmacognosy, SE-75123 Uppsala, Sweden
[3] Univ Costa Rica, Escuela Qimica, San Jose, Costa Rica
[4] Univ Costa Rica, CIPRONA, San Jose, Costa Rica
关键词
sesquiterpene lactones; neutrophil granulocytes; human neutrophil elastase release; PAF; fMLP; anti-inflammatory activity;
D O I
10.1016/S0006-2952(02)01652-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Sesquiterpene lactones (SLs) are natural products responsible for the anti-inflammatory activity of a variety of medicinal plants, mainly from the Asteraceae family. Here, we investigated whether they also influence the process of exocytosis of pro-inflammatory enzymes, such as the human neutrophil elastase (HNE). Altogether, eight structurally different SLs from the eudesmanolide, guaianolide, pseudoguaianolide, and germacranolide type were studied. Neutrophils were isolated from fresh human blood. After pre-incubation with different concentrations of the respective SL and cytochalasin B, the exocytosis of elastase was initiated either by platelet activating factor or N-formyl-methionyl-leucyl-phenylalanine. Inhibition of HNE release was measured by p-nitroaniline formation. The SLs exhibited an inhibitory effect on elastase release from neutrophils challenged either by platelet activating factor or N-formyl-methionyt-leucyl-phenylalanine. Concentration-response curves were recorded and the IC50 values ranged from 2 to 30 muM. Studies on isolated HNE showed that a selective direct inhibition on HNE can be excluded. Interestingly, the inhibitory activity did not correlate with the number of alpha,beta-unsaturated carbonyl functions. The structure-activity relationship and the molecular mechanism are discussed. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:897 / 903
页数:7
相关论文
共 31 条
  • [1] BANERJEE S, 1986, PLANTA MED, P29, DOI 10.1055/s-2007-969060
  • [2] Bernstein P R, 1994, Prog Med Chem, V31, P59, DOI 10.1016/S0079-6468(08)70019-5
  • [3] Study of sesquiterpene lactones from Milleria quinqueflora on their anti-inflammatory activity using the transcription factor NF-κB as molecular target
    Castro, V
    Rüngeler, P
    Murillo, R
    Hernandez, E
    Mora, G
    Pahl, HL
    Merfort, I
    [J]. PHYTOCHEMISTRY, 2000, 53 (02) : 257 - 263
  • [4] MOLECULAR EVENTS IN THE ACTIVATION OF HUMAN NEUTROPHILS FOR MICROBIAL KILLING
    COHEN, MS
    [J]. CLINICAL INFECTIOUS DISEASES, 1994, 18 : S170 - S179
  • [5] SESQUITERPENE LACTONES FROM MIKANIA-MICRANTHA
    CUENCA, MD
    BARDON, A
    CATALAN, CAN
    KOKKE, WCMC
    [J]. JOURNAL OF NATURAL PRODUCTS, 1988, 51 (03): : 625 - 626
  • [6] Dirsch VM, 2001, CANCER RES, V61, P5817
  • [7] Ethuin F, 2001, J LEUKOCYTE BIOL, V70, P439
  • [8] Inhibition of LPS-induced p42/44 MAP kinase activation and iNOS/NO synthesis by parthenolide in rat primary microglial cells
    Fiebich, BL
    Lieb, K
    Engels, S
    Heinrich, M
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 2002, 132 (1-2) : 18 - 24
  • [9] Antimycobacterial evaluation of germacranolides
    Fischer, NH
    Lu, TS
    Cantrell, CL
    Castañeda-Acosta, J
    Quijano, L
    Franzblau, SG
    [J]. PHYTOCHEMISTRY, 1998, 49 (02) : 559 - 564
  • [10] Cysteine 38 in p65/NF-κB plays a crucial role in DNA binding inhibition by sesquiterpene lactones
    García-Piñeres, AJ
    Castro, V
    Mora, G
    Schmidt, TJ
    Strunck, E
    Pahl, HL
    Merfort, I
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (43) : 39713 - 39720