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Intravital Microscopy of Leukocyte-endothelial and Platelet-leukocyte Interactions in Mesenterial Veins in Mice
Published on: August 13, 2015
Changes in leucocyte numbers without diapedesis in rats given platelet-activating factor (PAF-acether)
B A Spicer1, P A Hatt, H Smith
1Beecham Pharmaceuticals, Biosciences Research Centre, Epsom, Surrey, UK.
Summary
Platelet-activating factor (PAF-acether) and antigen challenges in rats show distinct peritoneal cavity responses. Antigen triggers histamine release and cellular infiltration, unlike PAF-acether alone.
Area of Science:
- Immunology
- Pharmacology
Background:
- Platelet-activating factor (PAF-acether) is a potent mediator involved in inflammatory responses.
- Understanding the differential effects of PAF-acether and antigen challenges is crucial for inflammatory disease research.
Purpose of the Study:
- To compare the inflammatory effects of intraperitoneal PAF-acether versus antigen challenge in rats.
- To investigate the roles of histamine and cellular infiltration in these responses.
Main Methods:
- Rats were sensitized and pre-treated to induce blood eosinophilia.
- Intraperitoneal injections of PAF-acether or antigen were administered.
- Peritoneal washings and blood were analyzed for cell counts, plasma protein extravasation, and histamine levels at various time points (5 min, 4 h, 24 h).
Main Results:
- PAF-acether induced rapid plasma protein extravasation but no histamine increase or significant cellular infiltration.
- Antigen challenge caused plasma protein extravasation, histamine release, and delayed cellular infiltration (neutrophils, mononuclear cells, eosinophils).
- Co-administration of PAF-acether and antigen amplified the inflammatory response compared to antigen alone.
Conclusions:
- PAF-acether and antigen elicit distinct early inflammatory cascades in the peritoneal cavity.
- Antigen-induced inflammation involves histamine release and a robust cellular infiltrate, which PAF-acether alone does not replicate.
- PAF-acether may modulate or enhance antigen-specific inflammatory responses.

