Inhibition of lovastatin on proliferation and expression of proinflammatory cytokines in cultured human glomerular mesangial cells

Chin Med J (Engl). 2003 Sep;116(9):1366-9.

Abstract

Objective: To study the effects and mechanism of lovastatin on cell proliferation and expression of proinflammatory cytokines in cultured human glomerular mesangial cells.

Methods: The influence of lovastatin on HMC proliferation was evaluated with 3H-thymidine incorporation. mRNA expression of proinflammatory cytokines (IL-1 beta, IL-6, TNF-alpha, and MCP-1) and activation of NF-kappa B of HMC were measured using Reverse transcription-polymerase chain reaction (RT-PCR) and electrophoretic mobility shift assay (EMSA) respectively.

Results: Lovastatin was found to have inhibitory effects on human mesangial cell (HMC) proliferation and lipopolysaccharide (LPS)-mediated human mesangine cell HMC mRNA expression of proinflammatory cytokines via activation of NF-kappa B. The effect of lovstatin on HMC could be prevented when the mevalonate and farnesol were added to the culture.

Conclusion: Lovastatin may decrease HMC proliferation and production of proinflammatory cytokines through the inhibition of NF-kappa B activation. This provided experimental evidence for further evaluation of the renal protective effect of HRI, suggesting that it may be a potent agent for prevention of progressive renal diseases aside from its lipid-lowering effect.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Division / drug effects*
  • Cell Survival / drug effects
  • Cells, Cultured
  • Chemokine CCL2 / analysis*
  • Glomerular Mesangium / cytology
  • Glomerular Mesangium / drug effects*
  • Humans
  • Interleukin-1 / analysis*
  • Interleukin-6 / analysis*
  • Lovastatin / pharmacology*
  • NF-kappa B
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Necrosis Factor-alpha / analysis*

Substances

  • Chemokine CCL2
  • Interleukin-1
  • Interleukin-6
  • NF-kappa B
  • Tumor Necrosis Factor-alpha
  • Lovastatin