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  • Key words:P. acnes/LPS hepatitis model — Macrophages/ Kupffer cells — Tumor necrosis factor-α— Phosphodiesterase — Rolipram  (1)
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    ISSN: 1420-908X
    Keywords: Key words:P. acnes/LPS hepatitis model — Macrophages/ Kupffer cells — Tumor necrosis factor-α— Phosphodiesterase — Rolipram
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Objective and Design: To study the effect of cellular cAMP-increasing agents on Propionibacterium acnes (P. acnes) and lipopolysaccharide (LPS)-induced mouse hepatitis.¶Material: Male BALB/c mice were used. Macrophages/Kupffer cells isolated from P. acnes-primed murine liver were used for the in vitro study.¶Treatment: Type IV phosphodiesterase (PDE)-specific inhibitor, rolipram, was administered (10, 30 mg/kg, p.o.). Dibutyryl cyclic AMP (dbcAMP) was injected (10, 100 mg/kg, i.p.) into the mice.¶Method: Plasma TNFα estimated by the use of an L-929 cell cytotoxic assay and plasma transaminase activities were measured for the in vivo study. The LPS-induced production of TNFα in vitro from the cultured macrophage/Kupffer cells was determined by ELISA.¶Results: Rolipram suppressed the elevation of plasma transaminases induced by injection of LPS, and dbcAMP had a tendency to suppress them. Both agents attenuated the LPS-induced release of TNFα in vivo, and suppressed the TNFα production from the cultured macrophage/Kupffer cells.¶Conclusions: These results suggest that rolipram and dbcAMP have potential to inhibit TNFa production from activated macrophage/Kupffer cells, and it may be partially involved in the protecting effect in the P. acnes/LPS hepatitis model.
    Type of Medium: Electronic Resource
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