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
  • [31] Pratt WB, 1998, P SOC EXP BIOL MED, V217, P420
  • [32] The GRIP1:IRF3 interaction as a target for glucocorticoid receptor-mediated immunosuppression
    Reily, MM
    Pantoja, C
    Hu, XY
    Chinenov, Y
    Rogatsky, I
    [J]. EMBO JOURNAL, 2006, 25 (01) : 108 - 117
  • [33] MOLECULAR-INTERACTIONS, T-CELL SUBSETS AND A ROLE OF THE CD4/CD8-P561CK COMPLEX IN HUMAN T-CELL ACTIVATION
    RUDD, CE
    ANDERSON, P
    MORIMOTO, C
    STREULI, M
    SCHLOSSMAN, SF
    [J]. IMMUNOLOGICAL REVIEWS, 1989, 111 : 225 - 266
  • [34] SAKAMOTO N, 1988, CANCER J, V2, P9
  • [35] Dissociation of transactivation from transrepression by a selective glucocorticoid receptor agonist leads to separation of therapeutic effects from side effects
    Schäcke, H
    Schottelius, A
    Döcke, WD
    Strehlke, P
    Jaroch, S
    Schmees, N
    Rehwinkel, H
    Hennekes, H
    Asadullah, K
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (01) : 227 - 232
  • [36] Mechanisms involved in the side effects of glucocorticoids
    Schäcke, H
    Döcke, WD
    Asadullah, K
    [J]. PHARMACOLOGY & THERAPEUTICS, 2002, 96 (01) : 23 - 43
  • [37] Insight into the molecular mechanisms of glucocorticoid receptor action promotes identification of novel ligands with an improved therapeutic index
    Schaecke, Heike
    Rehwinkel, Hartmut
    Asadullah, Khusru
    Cato, Andrew C. B.
    [J]. EXPERIMENTAL DERMATOLOGY, 2006, 15 (08) : 565 - 573
  • [38] Drug targeting by long-circulating liposomal glucocorticosteroids increases therapeutic efficacy in a model of multiple sclerosis
    Schmidt, J
    Metselaar, JM
    Wauben, MHM
    Toyka, KV
    Storm, G
    Gold, R
    [J]. BRAIN, 2003, 126 : 1895 - 1904
  • [39] Song IH, 2005, J RHEUMATOL, V32, P1199
  • [40] Membrane glucocorticoid receptors are down regulated by glucocorticoids in patients with systemic lupus erythematosus and use a caveolin-1-independent expression pathway
    Spies, C. M.
    Schaumann, D. H. S.
    Berki, T.
    Mayer, K.
    Jakstadt, M.
    Huscher, D.
    Wunder, C.
    Burmester, G-R
    Radbruch, A.
    Lauster, R.
    Scheffold, A.
    Buttgereit, F.
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2006, 65 (09) : 1139 - 1146