Divergent effects of estrogen and nicotine on Rho-kinase expression in human coronary vascular smooth muscle cells

Biochem Biophys Res Commun. 2005 Jan 7;326(1):154-9. doi: 10.1016/j.bbrc.2004.11.011.

Abstract

Recent studies have demonstrated that up-regulated Rho-kinase plays an important role in the pathogenesis of coronary arteriosclerosis and vasospasm. We have shown that inflammatory stimuli, such as angiotensin II and interleukin-1beta, up-regulate Rho-kinase expression and activity in human coronary vascular smooth muscle cells, for which intracellular signal transduction mediated by protein kinase C and NF-kappaB is involved. Here, we show that estrogen down-regulates while nicotine up-regulates Rho-kinase and that nicotine counteracts the inhibitory effect of estrogen on angiotensin II-induced Rho-kinase expression. Furthermore, we demonstrated that the intracellular signal transduction of the inhibitory effect of estrogen is mediated by an estrogen receptor. These results demonstrate that inflammatory stimuli up-regulate Rho-kinase, for which estrogen (mediated by an estrogen receptor) and nicotine exert divergent inhibitory and stimulatory effects on the Rho-kinase expression, respectively, and may explain in part why the incidence of arteriosclerotic and vasospastic disorders is increased in postmenopausal women and smokers.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin II / pharmacology
  • Cell Line
  • Coronary Vessels / cytology
  • Coronary Vessels / drug effects
  • Coronary Vessels / metabolism
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Estrogens / pharmacology*
  • Gene Expression Regulation / drug effects*
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Muscle, Smooth, Vascular / drug effects*
  • Muscle, Smooth, Vascular / metabolism*
  • Nicotine / pharmacology*
  • Protein Serine-Threonine Kinases / metabolism*
  • Receptors, Estrogen / metabolism*
  • rho-Associated Kinases

Substances

  • Estrogens
  • Intracellular Signaling Peptides and Proteins
  • Receptors, Estrogen
  • Angiotensin II
  • Nicotine
  • Protein Serine-Threonine Kinases
  • rho-Associated Kinases