Molecular mechanisms of glucocorticoid action and selective glucocorticoid receptor agonists

被引:293
作者
Stahn, Cindy
Loewenberg, Mark
Hommes, Daniel W.
Buttgereit, Frank
机构
[1] Charite, Dept Rheumatol & Clin Immunol, D-10117 Berlin, Germany
[2] Acad Med Ctr, Dept Gastroenterol Hepatol, NL-1105 AZ Amsterdam, Netherlands
[3] Leiden Univ, Ctr Med, Dept Gastroenterol Hepatol, NL-2300 RC Leiden, Netherlands
关键词
glucocorticoid; mechanisms of action; genomic; non-genomic; mGCR; cGCR; SEGRA;
D O I
10.1016/j.mce.2007.05.019
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glucocorticoids (GC) are the most common used anti-inflammatory and immunosuppressive drugs in the treatment of rheumatic and other inflammatory diseases. Their therapeutic effects are considered to be mediated by four different mechanisms of action: the classical genomic mechanism of action caused by the cytosolic glucocorticoid receptor (cGCR); secondary non-genomic effects which are also initiated by the cGCR; membrane-bound glucocorticoid receptor (mGCR)-mediated non-genomic effects; non-specific, non-genomic effects caused by interactions with cellular membranes. The classical, genomic mechanism of GC-action can be divided into two processes: "transrepression", which is responsible for a large number of desirable anti-inflammatory and immunomodulating effects, and "transactivation" which is associated with frequently occurring side effects as well as with some immunosuppressive activities [Ehrchen, J., Steinmuller, L., Barczyk, K., Tenbrock, K., Nacken, W., Eisenacher, M., Nordhues, U., Sorg, C., Sunderkotter, C., Roth, J., 2007. Glucocorticoids induce differentiation of a specifically activated, anti-inflammatory subtype of human monocytes. Blood 109, 1265-1274]. Great efforts have been made to diminish glucocorticoid-induced adverse effects, but the improvement of conventional glucocorticoids has almost reached its limits. As a consequence, new variations of the conventional "good old drugs" are being tested and nitro-steroids and long circulating liposomal glucocorticoids indeed show promising results. Nevertheless, crux of the matter should be the design of qualitatively new drugs, such as selective glucocorticoid receptor agonists (SEGRAs). These innovative steroidal or non-steroidal molecules induce transrepression, while transactivation processes are less affected. First reports on two different GCR ligands, A276575 and ZK216348, show promising results. Here, we review the above-mentioned mechanisms of glucocorticoid action and give particular attention to the development of optimized glucocorticoids and SEGRAs. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:71 / 78
页数:8
相关论文
共 45 条
  • [1] Corticosteroid-insensitive asthma: molecular mechanisms
    Adcock, IM
    Lane, SJ
    [J]. JOURNAL OF ENDOCRINOLOGY, 2003, 178 (03) : 347 - 355
  • [2] THE IMMUNOBIOLOGY OF T-CELLS WITH INVARIANT GAMMA-DELTA ANTIGEN RECEPTORS
    ALLISON, JP
    HAVRAN, WL
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1991, 9 : 679 - 705
  • [3] Almawi WY, 2002, J LEUKOCYTE BIOL, V71, P9
  • [4] Membrane glucocorticoid receptors (mGCR) are expressed in normal human peripheral blood mononuclear cells and up-regulated after in vitro stimulation and in patients with rheumatoid arthritis
    Bartholome, B
    Spies, CM
    Gaber, T
    Schuchmann, S
    Berki, T
    Kunkel, D
    Bienert, M
    Radbruch, A
    Burmester, GR
    Lauster, R
    Scheffold, A
    Buttgereit, F
    [J]. FASEB JOURNAL, 2004, 18 (01) : 70 - 80
  • [5] GENE-REGULATION BY STEROID-HORMONES
    BEATO, M
    [J]. CELL, 1989, 56 (03) : 335 - 344
  • [6] Therapeutic benefit of a dissociated glucocorticoid and the relevance of in vitro separation of transrepression from transactivation activity
    Belvisi, MG
    Wicks, SL
    Battram, CH
    Bottoms, SEW
    Redford, JE
    Woodman, P
    Brown, TJ
    Webber, SE
    Foster, ML
    [J]. JOURNAL OF IMMUNOLOGY, 2001, 166 (03) : 1975 - 1982
  • [7] Glucocorticoids in the treatment of rheumatic diseases - An update on the mechanisms of action
    Buttgereit, F
    Straub, RH
    Wehling, M
    Burmester, GR
    [J]. ARTHRITIS AND RHEUMATISM, 2004, 50 (11): : 3408 - 3417
  • [8] Rapid glucocorticoid effects on immune cells
    Buttgereit, F
    Scheffold, A
    [J]. STEROIDS, 2002, 67 (06) : 529 - 534
  • [9] Standardised nomenclature for glucocorticoid dosages and glucocorticoid treatment regimens:: current questions and tentative answers in rheumatology
    Buttgereit, F
    da Silva, JAP
    Boers, M
    Burmester, GR
    Cutolo, M
    Jacobs, J
    Kirwan, J
    Köhler, L
    van Riel, P
    Vischer, T
    Bijlsma, JWJ
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2002, 61 (08) : 718 - 722
  • [10] The molecular basis for the effectiveness, toxicity, and resistance to glucocorticoids: focus on the treatment of rheumatoid arthritis
    Buttgereit, F
    Saag, KG
    Cutolo, M
    da Silva, JAP
    Bijlsma, JWJ
    [J]. SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 2005, 34 (01) : 14 - 21