Novel anti-inflammatory peptides from the region of highest similarity between uteroglobin and lipocortin I

Nature. 1988 Oct 20;335(6192):726-30. doi: 10.1038/335726a0.

Abstract

Significant future developments in the effective treatment of inflammatory diseases may arise from non-toxic dual inhibitors of both cyclooxygenase and lipoxygenase pathways in the arachidonate cascade. Inhibition of phospholipase A2(PLA2)(EC3.1.1.4), may provide such a dual action and recent research has concentrated on the role of PLA2-inhibitory proteins as possible anti-inflammatory agents. Blastokinin or uteroglobin is a steroid-induced rabbit secretory protein with PLA2-inhibitory activity. Its biochemical and biological properties have been extensively studied and its crystallographic structure has been resolved at 1.34 A (refs 15, 16). Lipocortins are a family of related proteins, which, it has been suggested, mediate the anti-inflammatory effects of glucocorticoids (for a review, see ref. 23). Some proteins of this group have been purified and the complementary DNA sequences of two human lipocortins are known. Lipocortins inhibit PLA2 in vitro, although their mechanism of action is still unclear. Recombinant lipocortin I inhibits eicosanoid synthesis in isolated perfused lungs from the guinea pig. Here, we report that synthetic oligopeptides corresponding to a region of high amino-acid sequence similarity between uteroglobin and lipocortin I have potent PLA2 inhibitory activity in vitro and striking anti-inflammatory effects in vivo.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Annexins
  • Anti-Inflammatory Agents*
  • Dose-Response Relationship, Drug
  • Glycoproteins / pharmacology*
  • Molecular Sequence Data
  • Peptides / pharmacology*
  • Phospholipases / antagonists & inhibitors*
  • Rats
  • Recombinant Proteins / pharmacology
  • Software
  • Uteroglobin / pharmacology*

Substances

  • Annexins
  • Anti-Inflammatory Agents
  • Glycoproteins
  • Peptides
  • Recombinant Proteins
  • Uteroglobin
  • Phospholipases