Pigment epithelium-derived factor (PEDF) administration inhibits occlusive thrombus formation in rats: a possible participation of reduced intraplatelet PEDF in thrombosis of acute coronary syndromes

Atherosclerosis. 2008 Mar;197(1):25-33. doi: 10.1016/j.atherosclerosis.2007.07.041. Epub 2007 Sep 11.

Abstract

Objectives: Although remarkable therapeutic advances in the treatment of acute coronary syndromes (ACS) have been made with anti-platelet therapy, the therapeutic options may be limited by considerable side effects. Pigment epithelium-derived factor (PEDF) has anti-oxidative properties and may play a protective role against atherosclerosis. In this study, we investigated whether PEDF prevented occlusive thrombus formation in rats.

Methods and results: Occlusive thrombus formation was induced by treating rats with ligation and cuff placement at the left common carotid artery. Intravenous injection of PEDF dose-dependently inhibited thrombus formation and blocked the increase in immunoreactivity of P-selectin, a marker of platelet activation, NADPH oxidase activity and superoxide generation in thrombi. In vitro, PEDF significantly decreased collagen-induced reactive oxygen species generation in platelets and subsequently suppressed the platelet activation and aggregation. Plasma and intraplatelet levels of PEDF in the coronary circulation in patients with ACS were significantly lower than those in age- and gender-matched controls without coronary artery disease.

Conclusions: These results demonstrated that PEDF administration could inhibit occlusive thrombus formation by blocking the platelet activation and aggregation through its anti-oxidative properties. Our present study suggests that pharmacological up-regulation or substitution of PEDF may offer a promising strategy for the treatment of arterial thrombosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Coronary Syndrome / drug therapy*
  • Acute Coronary Syndrome / metabolism
  • Animals
  • Arterial Occlusive Diseases / drug therapy*
  • Arterial Occlusive Diseases / metabolism
  • Blood Platelets / drug effects
  • Blood Platelets / metabolism
  • Carotid Artery Thrombosis / drug therapy*
  • Carotid Artery Thrombosis / metabolism
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Eye Proteins / metabolism*
  • Eye Proteins / pharmacology*
  • Humans
  • NADPH Oxidases / metabolism
  • Nerve Growth Factors / metabolism*
  • Nerve Growth Factors / pharmacology*
  • P-Selectin / metabolism
  • Platelet Aggregation / drug effects
  • Platelet Aggregation / physiology
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species / metabolism
  • Serpins / metabolism*
  • Serpins / pharmacology*
  • Superoxides / metabolism

Substances

  • Eye Proteins
  • Nerve Growth Factors
  • P-Selectin
  • Reactive Oxygen Species
  • Serpins
  • pigment epithelium-derived factor
  • Superoxides
  • NADPH Oxidases