L-arginine attenuates lipopolysaccharide-induced lung chemokine production

Am J Physiol Lung Cell Mol Physiol. 2001 Mar;280(3):L400-8. doi: 10.1152/ajplung.2001.280.3.L400.

Abstract

Chemokines stimulate the influx of leukocytes into tissues. Their production is regulated by nuclear factor-kappaB (NF-kappaB), an inducible transcription factor under the control of inhibitory factor kappaB-alpha (IkappaB-alpha). We have previously demonstrated that L-arginine (L-Arg) attenuates neutrophil accumulation and pulmonary vascular injury after administration of lipopolysaccharide (LPS). We hypothesized that L-Arg would attenuate the production of lung chemokines by stabilizing IkappaB-alpha and preventing NF-kappaB DNA binding. We examined the effect of L-Arg on chemokine production, IkappaB-alpha degradation, and NF-kappaB DNA binding in the lung after systemic LPS. To block nitric oxide (NO) production, a NO synthase inhibitor was given before L-Arg. LPS induced the production of chemokine protein and mRNA. L-Arg attenuated the production of chemokine protein and mRNA, prevented the decrease in IkappaB-alpha levels, and inhibited NF-kappaB DNA binding. NO synthase inhibition abolished the effects of L-Arg on all measured parameters. Our results suggest that L-Arg abrogates chemokine protein and mRNA production in rat lung after LPS. This effect is dependent on NO and is mediated by stabilization of IkappaB-alpha levels and inhibition of NF-kappaB DNA binding.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Arginine / blood
  • Arginine / pharmacology*
  • Chemokine CXCL1
  • Chemokine CXCL2
  • Chemokines / antagonists & inhibitors*
  • Chemokines / biosynthesis*
  • Chemokines / genetics
  • Chemokines / metabolism
  • Chemokines, CXC*
  • Chemotactic Factors / genetics
  • Chemotactic Factors / metabolism
  • DNA / metabolism
  • Growth Substances / genetics
  • Growth Substances / metabolism
  • I-kappa B Proteins / metabolism
  • Intercellular Signaling Peptides and Proteins*
  • Lipopolysaccharides / pharmacology*
  • Lung / metabolism*
  • Male
  • NF-kappa B / metabolism
  • Nitrates / metabolism
  • Nitrites / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Chemokine CXCL1
  • Chemokine CXCL2
  • Chemokines
  • Chemokines, CXC
  • Chemotactic Factors
  • Cxcl1 protein, mouse
  • Cxcl1 protein, rat
  • Cxcl2 protein, mouse
  • Cxcl2 protein, rat
  • Growth Substances
  • I-kappa B Proteins
  • Intercellular Signaling Peptides and Proteins
  • Lipopolysaccharides
  • NF-kappa B
  • Nitrates
  • Nitrites
  • RNA, Messenger
  • DNA
  • Arginine