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Veterinary pathology1985; 22(4); 375-386; doi: 10.1177/030098588502200413

Functional and biochemical characterization of immunologically derived equine platelet-activating factor.

Abstract: Antigen-specific challenge of equine leukocytes induced the non-lytic release of a platelet-activating factor in vitro. The equine platelet-activating factor stimulated the release of serotonin from equine platelets in a dose-responsive manner, independent of the presence of cyclo-oxygenase pathway inhibitors such as indomethacin. Rabbit platelets were also responsive to equine platelet-activating factor. The release of equine platelet-activating factor was a rapid reaction with near maximal secretion taking place in 30 seconds. Addition of equine platelet-activating factor to washed equine platelets stimulated platelet aggregation which could not be inhibited by the presence of aspirin or indomethacin. Platelets pre-incubated with equine platelet-activating factor became specifically desensitized to equine platelet-activating factor while remaining responsive to other platelet stimuli such as collagen and epinephrine. The following biochemical properties of equine platelet-activating factor are identical to those properties of 1-0-alkyl-2-acetyl-sn-glyceryl-3-phosphorylcholine (AGEPC): stability upon exposure to air and acid; loss of functional activity after base-catalyzed methanolysis with subsequent acylation that returned all functional activity; and identical relative mobilities on silica gel G plates developed with chloroform:methanol:water (65:35:6, volume/volume). The combined functional and biochemical characteristics of equine platelet-activating factor strongly suggest identity between this naturally occurring, immunologically derived equine factor and AGEPC.
Publication Date: 1985-07-01 PubMed ID: 4035942DOI: 10.1177/030098588502200413Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research looked into an antigen-induced factor in horses that activates platelets. The study found that this equine platelet-activating factor quickly reacts, within 30 seconds, causing not only platelet aggregation but also the release of serotonin.

Introductory Background

  • This research study investigated the functionality and biochemical properties of an antigen-induced substance produced by equine leukocytes (white blood cells) called equine platelet-activating factor (ePAF).
  • ePAF stimulates platelets, which play a crucial role in clotting and wound healing, and was observed to cause the release of serotonin, a neurotransmitter that contributes to feelings of well-being and happiness, from platelets.

In Vitro Testing

  • The study revealed that ePAF responded swiftly, showing near-maximum secretion within 30 seconds after an antigen-specific challenge to the leukocytes.
  • The researchers also found that washed equine platelets responded to ePAF by aggregating, a critical step in the formation of a blood clot needed to prevent bleeding.
  • This aggregation reaction could not be inhibited by aspirin or indomethacin, both of which are known inhibitors of the cyclo-oxygenase pathway and are used to inhibit platelet aggregation in humans. This suggests that ePAF activates platelets through a different pathway.

Desensitization and Reactivity

  • The study also discovered that platelets that had been previously exposed to ePAF became specifically desensitized to it, meaning they no longer responded to ePAF stimulus.
  • However, these desensitized platelets still responded to other platelet stimuli such as collagen and epinephrine, implying that the impact of ePAF is specific and does not affect the overall ability of the platelet to function.

Biochemical Properties

  • The study found that the biochemical properties of ePAF were identical to a known compound called 1-0-alkyl-2-acetyl-sn-glyceryl-3-phosphorylcholine (AGEPC), which is functionally and biochemically stable in air and acid.
  • This matching set of characteristics strongly suggest that the naturally occurring ePAF is the same as AGEPC.

Concluding Remarks

  • This research provides valuable insight into a specific immune response mechanism in horses and provides a foundation for further investigation into the interaction of immune cells and platelets, and its possible implications in human medicine.

Cite This Article

APA
Wimberly HC, Slauson DO, Neilsen NR. (1985). Functional and biochemical characterization of immunologically derived equine platelet-activating factor. Vet Pathol, 22(4), 375-386. https://doi.org/10.1177/030098588502200413

Publication

ISSN: 0300-9858
NlmUniqueID: 0312020
Country: United States
Language: English
Volume: 22
Issue: 4
Pages: 375-386

Researcher Affiliations

Wimberly, H C
    Slauson, D O
      Neilsen, N R

        MeSH Terms

        • Animals
        • Antigens, Helminth / immunology
        • Ascaris / immunology
        • Aspirin / pharmacology
        • Blood Platelets / drug effects
        • Blood Platelets / metabolism
        • Chromatography, Thin Layer
        • Dose-Response Relationship, Drug
        • Female
        • Horses / physiology
        • In Vitro Techniques
        • Indomethacin / pharmacology
        • L-Lactate Dehydrogenase / metabolism
        • Leukocytes / immunology
        • Leukocytes / metabolism
        • Male
        • Platelet Activating Factor / analysis
        • Platelet Activating Factor / pharmacology
        • Platelet Activating Factor / physiology
        • Platelet Aggregation
        • Serotonin / metabolism