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PMID: 11259554 Published · ppublish English Journal Article

Anti-inflammatory and immunomodulatory potential of the novel PDE4 inhibitor roflumilast in vitro.

The Journal of pharmacology and experimental therapeutics ·Vol. 297 ·No. 1 ·2001-04-00 ·Pages 267-79

Hatzelmann A, Schudt C

Abstract

From a series of benzamide derivatives, roflumilast (3-cyclo-propylmethoxy-4-difluoromethoxy-N-[3,5-di-chloropyrid-4-yl]-benzamide) was identified as a potent and selective PDE4 inhibitor. It inhibits PDE4 activity from human neutrophils with an IC(50) of 0.8 nM without affecting PDE1 (bovine brain), PDE2 (rat heart), and PDE3 and PDE5 (human platelets) even at 10,000-fold higher concentrations. Roflumilast is almost equipotent to its major metabolite formed in vivo (roflumilast N-oxide) and piclamilast (RP 73401), however, more than 100-fold more potent than rolipram and Ariflo (cilomilast; SB 207499). The anti-inflammatory and immunomodulatory potential of roflumilast and the reference compounds was investigated in various human leukocytes using cell-specific responses: neutrophils [N-formyl-methyl-leucyl-phenylalanine (fMLP)-induced formation of LTB(4) and reactive oxygen species (ROS)], eosinophils (fMLP- and C5a-induced ROS formation), monocytes, monocyte-derived macrophages, and dendritic cells (lipopolysaccharide-induced tumor necrosis factor-alpha synthesis), and CD4+ T cells (anti-CD3/anti-CD28 monoclonal antibody-stimulated proliferation, IL-2, IL-4, IL-5, and interferon-gamma release). Independent of the cell type and the response investigated, the corresponding IC values (for half-maximum inhibition) of roflumilast were within a narrow range (2-21 nM), very similar to roflumilast N-oxide (3-40 nM) and piclamilast (2-13 nM). In contrast, cilomilast (40-3000 nM) and rolipram (10-600 nM) showed greater differences with the highest potency for neutrophils. Compared with neutrophils and eosinophils, representing the terminal inflammatory effector cells, the relative potency of roflumilast and its N-oxide for monocytes, CD4+ T cells, and dendritic cells is substantially higher compared with cilomilast and rolipram, probably reflecting an improved immunomodulatory potential. The efficacy of roflumilast in vitro and in vivo (see accompanying article in this issue) suggests that roflumilast will be useful in the treatment of chronic inflammatory disorders such as asthma and chronic obstructive pulmonary disease.

MeSH Terms
3',5'-Cyclic-AMP Phosphodiesterases/antagonists & inhibitors Aminopyridines/pharmacology Anti-Inflammatory Agents, Non-Steroidal/pharmacology Benzamides/pharmacology CD4-Positive T-Lymphocytes/drug effects,immunology Cyclic Nucleotide Phosphodiesterases, Type 1 Cyclic Nucleotide Phosphodiesterases, Type 4 Cyclopropanes Cytokines/biosynthesis Dendritic Cells/drug effects,physiology Eosinophils/drug effects,physiology Humans Immunosuppressive Agents/pharmacology In Vitro Techniques Luminescent Measurements Lymphocyte Activation/drug effects Monocytes/drug effects,metabolism Neutrophils/drug effects,physiology Phosphodiesterase Inhibitors/pharmacology Pyridazines/pharmacology Tumor Necrosis Factor-alpha/biosynthesis
Chemicals
Aminopyridines Anti-Inflammatory Agents, Non-Steroidal Benzamides Cyclopropanes Cytokines Immunosuppressive Agents Phosphodiesterase Inhibitors Pyridazines Tumor Necrosis Factor-alpha Roflumilast motapizone 3',5'-Cyclic-AMP Phosphodiesterases Cyclic Nucleotide Phosphodiesterases, Type 1 Cyclic Nucleotide Phosphodiesterases, Type 4
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hatzelmann A
Byk Gulden, Department of Biochemistry, P.O. Box 100301, 48403 Konstanz, Germany. armin.hatzelmann@byk.de
Schudt C
Article Info
Journal
The Journal of pharmacology and experimental therapeutics
Abbr.
J Pharmacol Exp Ther
ISSN
0022-3565
Published
2001-04-00
Pages
267-79
Language
English
Region
United States
NLM ID
0376362
Subset
IM
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