Abstract
Vascular eicosanoids (E) thromboxane (measured as T×B2) and prostacyclin (measured as 6-keto-PGF1α) may modulate hemodynamic parameters in brain circulation. We have studied (a) the effects of the administration of vasoactive drugs, in the rat, on T×B2 and 6-keto-PGF1α levels and release in brain cortex, and (b) changes of brain vascular E levels during hypoxia and recovery, in the same animal species. (a) Administration of vasoactive drugs (papaverine, dipyridamole, the carbochromene derivative AD6 and nifedipine) to rats resulted in differential effects on endogenous levels and post-decapitation release of both compounds. Reduction of the T×B2/6-keto-PGF1α balance in brain cortex was obtained with papaverine and AD6, whereas nifedipine reduced 6-keto-PGF1α more than T×B2. (b) During hypoxia there was no significant modification of brain vascular E, but during recovery both compounds were decreased. Thus pharmacological treatments during recovery from hypoxia may normalize brain vascular E levels.
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