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PMID: 10796066 Published · ppublish English Journal Article Review

Cyclic nucleotide phosphodiesterase (PDE) inhibitors and immunomodulation.

Biochemical pharmacology ·Vol. 57 ·No. 9 ·1999-05-01 ·Pages 965-73

Essayan DM

Abstract

Intracellular levels of cyclic nucleotide second messengers are regulated predominantly by the complex superfamily of cyclic nucleotide phosphodiesterase (PDE) enzymes. Recent advances in our understanding of the molecular pharmacology of these enzymes has led to their identification as biologic regulators of certain disease states and the development of isozyme-selective inhibitors as potential therapeutic agents. A large body of in vitro and preclinical data suggests the therapeutic utility of PDE4 inhibitors as potent anti-inflammatory agents. Early clinical trials with selective PDE inhibitors substantiate this approach while highlighting pharmacodynamic and toxicologic pitfalls inherent to the inhibition of specific PDE isozymes. This commentary will review our current understanding of PDE inhibitors as immunomodulatory agents.

MeSH Terms
Adjuvants, Immunologic/pharmacology Cyclic AMP/pharmacology Cyclic GMP/pharmacology Humans Immunosuppression Therapy Leukocytes/drug effects,immunology Phosphodiesterase Inhibitors/pharmacology Phosphoric Diester Hydrolases/metabolism Structure-Activity Relationship
Chemicals
Adjuvants, Immunologic Phosphodiesterase Inhibitors Cyclic AMP Phosphoric Diester Hydrolases Cyclic GMP
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Essayan D M
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA. [email protected]
Article Info
Journal
Biochemical pharmacology
Abbr.
Biochem Pharmacol
ISSN
0006-2952
Published
1999-05-01
Pages
965-73
Language
English
Region
England
NLM ID
0101032
Subset
IM
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