Mevalonate Inhibitors Inhibit the Induction of iNOS and Cytokines

This study explores the role of mevalonate inhibitors in the activation of NF-k b and the induction of inducible nitric oxide synthase (iNOS) and cytokines (TNFa , IL-1 b , and IL-6) in rat primary astrocytes, microglia, and macrophages. Lovastatin and sodium phenylacetate (NaPA) were found to inhibit LPSand cytokine-mediated production of NO and expression of iNOS in rat primary astrocytes; this inhibition was not due to depletion of end products of mevalonate pathway (e.g., cholesterol and ubiquinone). Reversal of the inhibitory effect of lovastatin on LPS-induced iNOS expression by mevalonate and farnesyl pyrophosphate and reversal of the inhibitory effect of NaPA on LPS-induced iNOS expression by farnesyl pyrophosphate, however, suggests a role of farnesylation in the LPS-mediated induction of iNOS. The inhibition of LPS-mediated induction of iNOS by FPT inhibitor II, an inhibitor of Ras farnesyl protein transferase, suggests that farnesylation of p21 ras or other proteins regulates the induction of iNOS. Inhibition of LPSmediated activation of NF-k b by lovastatin, NaPA, and FPT inhibitor II in astrocytes indicates that the observed inhibition of iNOS expression is mediated via inhibition of NF-k b activation. In addition to iNOS, lovastatin and NaPA also inhibited LPS-induced expression of TNFa , IL-1 b , and IL-6 in rat primary astrocytes, microglia, and macrophages. This study delineates a novel role of the mevalonate pathway in controlling the expression of iNOS and different cytokines in rat astrocytes, microglia, and macrophages that may be important in developing therapeutics against cytokineand NO-mediated neurodegenerative diseases. ( J. Clin. Invest. 1997. 100:2671–2679.)