Possible Mechanism of Vasogenic Brain Oedema Induced by Arachidonic Acid

  • T. Ohnishi
  • H. Iwasaki
  • T. Hayakawa
  • W. R. Shapiro
Conference paper
Part of the Acta Neurochirurgica book series (NEUROCHIRURGICA, volume 51)


Free archidonic acid was infused into normal rat brains and the effect of arachidonic acid on capillary permeability was investigated by measuring the regional uptake of 14C-aminoisobutyric acid with a quantitative autoradiographic method. Arachidonic acid increased capillary permeability in a dose-dependent manner up to 2 mM. A high dose of arachidonic acid ( > 5 mM) produced a profound tissue destruction around the needle track and less increased capillary permeability than 2 mM arachidonic acid. Time-course study disclosed that arachidonic acid markedly increased capillary permeability within 2 hours after infusion, and continued to increase with time to 24 hours. The effect of 48 hours infusion was about a half of that at 24 hours, indicating that the effect of arachidonic acid was partially reversible. Pretreatment with dexamethasone significantly inhibited the arachidonic acid-induced increase in capillary permeability and the administration of actinomycin D 1 hour before the pretreatment with dexamethasone suppressed the inhibitory effect of dexamethasone. These results suggest that arachidonic acid, which is deposited in the extracellular space, increases brain capillary permeability by two different ways. One is the direct detergent effect of arachidonic acid, and the other is the effect of arachidonic acid that is released from the membrane by the activation of phospholipase A2.


Arachidonic Acid Capillary Permeability Needle Track Krebs Ringer Buffer Vasogenic Brain Oedema 


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Copyright information

© Springer-Verlag 1990

Authors and Affiliations

  • T. Ohnishi
    • 3
  • H. Iwasaki
    • 1
  • T. Hayakawa
    • 1
  • W. R. Shapiro
    • 2
  1. 1.Department of NeurosurgeryOsaka University Medical SchoolOsakaJapan
  2. 2.Department of NeurologyMemorial Sloan-Kettering Cancer CenterUSA
  3. 3.Department of NeurosurgeryOsaka University Medical SchoolFukushima, Osaka 553Japan

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