TY - JOUR T1 - An Anti-Inflammatory Benzamide Derivative Inhibits the Protein Kinase C (PKC)-Dependent Pathway of ERK2 Phosphorylation in Murine Macrophages JF - Journal of Pharmacology and Experimental Therapeutics JO - J Pharmacol Exp Ther SP - 358 LP - 365 VL - 283 IS - 1 AU - Laurent Vernhet AU - Jean-Yves Petit AU - François Lang Y1 - 1997/10/01 UR - http://jpet.aspetjournals.org/content/283/1/358.abstract N2 - We have previously described benzamide derivatives that inhibited tumor necrosis factor (TNF) production from activated macrophages (Mφ) probably by interacting with a protein kinase C (PKC)-dependent pathway. To investigate their mode of action further, we first tested their effect on isolated PKC in vitro, using the selective inhibitor bisindolylmaleimide (BIM) as a positive control. We found that our representative compound JM34 did not inhibit PKC activityin vitro. We then investigated pathways located downstream of PKC and focused on the Raf1/MEK1,2/Erk1,2 cascade known to be preferentially activated by PKC activators such as phorbol esters. We found that JM34 dose-dependently inhibited Erk2 phosphorylation in Mφ stimulated by phorbol dibutyrate and calcium ionophore (maximal inhibition of 85% at 300 μM). BIM at 3 μM totally abrogated Erk2 phosphorylation. After stimulation with endotoxin or zymosan, Erk2 phosphorylation was only partially inhibited (25–30%) by JM34 or BIM, which confirmed that PKC-independent events were also involved in Erk2 phosphorylation. Because activated Erk2 has been shown to activate phospholipase A2, we tested the effect of JM34 and BIM on the release of arachidonate metabolites from activated Mφ. We found that both products partially inhibited the release of arachidonate metabolites from zymosan-activated Mφ at levels comparable to their inhibition of Erk2 phosphorylation. In contrast, JM34 and BIM markedly differed in their ability to inhibit TNF production. Taken together, our results suggest that JM34 inhibited the PKC-dependent pathway of Erk2 phosphorylation, which may fully account for its inhibitory effect on phospholipase A2 activation. However, the inhibition of TNF release by JM34 probably involved inhibition of an additional pathway, distinct from the Erk1/Erk2 cascade. The American Society for Pharmacology and Experimental Therapeutics ER -