The relative contribution of constitutive and inducible cyclooxygenase activity to lipopolysaccharide-induced prostaglandin production by primary cultures of rat hypothalamic astrocytes

Neurosci Lett. 1998 Apr 17;246(1):45-8. doi: 10.1016/s0304-3940(98)00226-2.

Abstract

In this study, we have compared the time-course effects of lipopolysaccharide (LPS) and interleukin-1beta on prostaglandin (PG) production by primary cultures of rat astrocytes. At variance with interleukin-1beta, LPS produced significant increases in PGE2 release after only 1 h of incubation, an effect unlikely to depend on new protein synthesis; the involvement of constitutive cyclooxygenase (COX-1) was therefore investigated. Experiments with acetylsalicylic acid showed that 80% of PGE2 production after 1 h of treatment with LPS is accounted for by COX-1; this figure decreases to about 30% after a 24-h treatment. The increase in PGE2 production occurring after a 24-h challenge with the endotoxin seems to involve the activation of phospholipase A2. In fact, LPS-stimulated PGE2 release was significantly reduced by a peptide from the primary sequence of lipocortin-1, peptide Ac2-26, which was previously shown to inhibit phospholipase A2 in several in vitro models.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Annexin A1 / pharmacology
  • Aspirin / pharmacology
  • Astrocytes / drug effects
  • Astrocytes / metabolism*
  • Cells, Cultured
  • Cyclooxygenase Inhibitors / pharmacology
  • Dexamethasone / pharmacology
  • Dinoprostone / biosynthesis*
  • Hypothalamus / drug effects
  • Hypothalamus / metabolism
  • Interleukin-1 / pharmacology*
  • Lipopolysaccharides / pharmacology*
  • Phospholipases A / antagonists & inhibitors
  • Phospholipases A / physiology
  • Phospholipases A2
  • Prostaglandin-Endoperoxide Synthases / physiology*
  • Rats
  • Rats, Wistar
  • Time Factors

Substances

  • Annexin A1
  • Cyclooxygenase Inhibitors
  • Interleukin-1
  • Lipopolysaccharides
  • Dexamethasone
  • Prostaglandin-Endoperoxide Synthases
  • Phospholipases A
  • Phospholipases A2
  • Dinoprostone
  • Aspirin