Inflammatory effect of intratracheal instillation of ultrafine particles in the rabbit: role of C-fiber and mast cells

Toxicol Appl Pharmacol. 1999 Nov 1;160(3):250-61. doi: 10.1006/taap.1999.8762.

Abstract

The effects of ultrafine polystyrene carboxylate-modified (fluorospheres) on inflammatory processes are being investigated in rabbit lungs. One milliliter of sterile NaCl (0.9%) containing 4 mg of ultrafine particles (UFP) was intratracheally instilled into anesthetized rabbits. The control animals were only instilled with sterile NaCl (0.9%). Twenty hours after being instilled, the rabbits were killed and their lungs were excised and then tracheally perfused with phosphate-buffered physiological solution (PBS). The lung effluents, collected from small holes made in the pleura, were analyzed for substance P (SP) and histamine content by radioimmunoassay (RIA) methods, after administration of drugs. In addition, in other groups of rabbits, the lung wet/dry (W/D) weight ratio was monitored, as were the cellular and protein contents in bronchoalveolar lavage (BAL). Electron microscopy examination was also performed. In tracheally superfused experiments, UFP induced a significant enhancement of both SP and histamine releases after administration of capsaicin (10(-4) M), to stimulate C-fiber, and carbachol (10(-4) M), a cholinergic agonist. A significant increase in histamine release was also recorded in the UFP-instilled group following the administration of both SP (10(-6) M) plus thiorphan (10(-5) M) and compound 48/80 (C48/80) (10(-3) M) to stimulate mast cells. In addition, the BAL fluid analysis of UFP groups showed an influx of neutrophils and an increase in total protein concentration. An increase in the lung WW/DW ratio was also recorded. Both epithelial and endothelial injuries were observed in the lungs of UFP-instilled rabbits. The pretreatment of rabbits in vivo with a mixture of either SR 140333 and SR 48368, a tachykinin NK(1) and NK(2) receptor antagonist, or a mixture of terfenadine and cimetidine, a histamine H(1) and H(2) receptor antagonist, prevented UFP- induced neutrophil influx and increased total proteins and lung WW/DW ratio. Therefore, it can be concluded that chemicaly inert, electrically charged UFP induce a pulmonary inflammatory process during which the release of SP and histamine from C-fibers and mast cells was enhanced after various stimuli. These latter mediators can also modulate the inflammatory process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Capsaicin / pharmacology
  • Carbachol / pharmacology
  • Chemotaxis, Leukocyte / drug effects
  • Female
  • Histamine / metabolism
  • Histamine Antagonists / pharmacology
  • Intubation, Intratracheal
  • Lung / drug effects*
  • Lung / immunology
  • Lung / ultrastructure
  • Male
  • Mast Cells / drug effects
  • Mast Cells / physiology*
  • Microspheres
  • Nerve Fibers / drug effects
  • Nerve Fibers / physiology*
  • Neutrophils / physiology
  • Pneumonia / chemically induced*
  • Pneumonia / immunology
  • Pneumonia / pathology
  • Polystyrenes / administration & dosage
  • Polystyrenes / toxicity*
  • Rabbits
  • Receptors, Tachykinin / antagonists & inhibitors
  • Substance P / metabolism
  • Thiorphan / pharmacology
  • p-Methoxy-N-methylphenethylamine / pharmacology

Substances

  • Histamine Antagonists
  • Polystyrenes
  • Receptors, Tachykinin
  • Substance P
  • p-Methoxy-N-methylphenethylamine
  • Histamine
  • Carbachol
  • Thiorphan
  • Capsaicin