Effects of cAMP-Phosphodiesterase Isozyme Inhibitor on Cytokine Production by Lipopolysaccharide-Stimulated Human Peripheral Blood Mononuclear Cells

1. The effects of cAMP-phosphodiesterase (PDE) isozyme inhibitors on the production of tumor necrosis factor α (TNF-α), and interleukins 1β and 8 (IL-1β and IL-8) by lipopolysaccharide (LPS)-stimulated human peripheral blood mononuclear cells (PBMC) were evaluated. In addition, we investigated the e...

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Published inGeneral pharmacology Vol. 29; no. 4; pp. 633 - 638
Main Authors Yoshimura, Tomoaki, Kurita, Chikako, Nagao, Tomomi, Usami, Eiseki, Nakao, Toshiya, Watanabe, Shino, Kobayashi, Joji, Yamazaki, Futoshi, Tanaka, Hiroyuki, Nagai, Hiroichi
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.10.1997
Elsevier
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Summary:1. The effects of cAMP-phosphodiesterase (PDE) isozyme inhibitors on the production of tumor necrosis factor α (TNF-α), and interleukins 1β and 8 (IL-1β and IL-8) by lipopolysaccharide (LPS)-stimulated human peripheral blood mononuclear cells (PBMC) were evaluated. In addition, we investigated the effects of dibutyryl cAMP (dbcAMP) and β-adrenergic receptor agonist on the production of these cytokines. 2. Type IV PDE inhibitors were more effective at inhibiting the production of TNF-α and IL-1β by LPS-stimulated PBMC than a nonselective, type III or type III/IV inhibitor. In contrast, these agents had no effect on IL-8 production. 3. Increasing concentrations of dbcAMP progressively reduced the production of TNF-α and IL-1β but not IL-8. 4. The addition of β-agonist increased the inhibitory effect of PDE inhibitors tested on the production of TNF-α and IL-1β. 5. Type IV PDE inhibitors could be potent pharmacological agents for the treatment of diseases in which TNF-α and IL-1β are important etiological factors.
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ISSN:0306-3623
1879-0011
DOI:10.1016/S0306-3623(96)00580-0