Dilazep and dipyridamole inhibit tissue factor expression on monocytes induced by IgG from patients with antiphospholipid syndrome

Acta Pharmacol Sin. 2004 Oct;25(10):1366-71.

Abstract

Aim: To investigate whether antiplatelet agents, dilazep and dipyridamole, inhibit tissue factor (TF) expression on monocytes induced by IgG from patients with antiphospholipid syndrome (APS).

Methods: Freshly isolated peripheral blood monocytes were allowed to adhere on plastic and then cultured in media containing patient or control antibodies and/or other agonists with or without dilazep or dipyridamole. The TF activity on monocytes was investigated by measuring factor VIIa-dependent generation of factor Xa, using a chromogenic substrate and the TF mRNA expression was examined by real-time PCR (TaqMan PCR).

Results: The TF activity on monocytes induced by APS IgG (250 mg/L) was inhibited by dilazep (0.15-150 micromol/L) and dipyridamole (0.2-200 micromol/L) in a dose-dependent fashion. But, the TF mRNA expression induced by APS IgG was not inhibited. Theophylline (500 micromol/L), an adenosine receptor antagonist, could counteract the inhibitory effect of dilazep and dipyridamole on TF activity.

Conclusion: Antiplatelet agents, dilazep and dipyridamole, block APS IgG-induced monocytes TF expression at a post-transcriptional level, partly by adenosine receptor pathway. Pharmacological agents that block monocytes TF activity, such as dilazep and dipyridamole, are a novel therapeutic approach in APS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic Antagonists / pharmacology
  • Antiphospholipid Syndrome / blood*
  • Antiphospholipid Syndrome / immunology
  • Cell Separation
  • Dilazep / pharmacology*
  • Dipyridamole / pharmacology*
  • Gene Expression / drug effects
  • Humans
  • Immunoglobulin G / immunology
  • Immunoglobulin G / pharmacology
  • Monocytes / metabolism*
  • Platelet Aggregation Inhibitors / pharmacology
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Theophylline / pharmacology
  • Thromboplastin / biosynthesis*
  • Thromboplastin / genetics

Substances

  • Adrenergic Antagonists
  • Immunoglobulin G
  • Platelet Aggregation Inhibitors
  • RNA, Messenger
  • Dipyridamole
  • Thromboplastin
  • Theophylline
  • Dilazep