Journal of Cerebral Blood Flow & Metabolism · 2013 · 52 citations · 33 references
MedicineNeurosciencePharmacologyGlial BiologyPharmacodynamicsSignal TransductionAstrocyte BiologyCerebrovascular PhysiologyG Protein-coupled Receptor SignalingNervous TissueNeurologic PathophysiologyNeurovascular CouplingAstrocyte CouplingAstrocyte Endfeet BiologyAstrocyte Endfeet SignalingAstrocyte-mediated Vascular RegulationAstrocytic EndfeetDirect EffectsNeurovascular Coupling MechanismsProstaglandin Physiology
It has been proposed that prostaglandin E(2) (PGE(2)) is released from astrocytic endfeet to dilate parenchymal arterioles through activation of prostanoid (EP(4)) receptors during neurovascular coupling. However, the direct effects of PGE(2) on isolated parenchymal arterioles have not been tested. Here, we examined the effects of PGE(2) on the diameter of isolated pressurized parenchymal arterioles from rat and mouse brain. Contrary to the prevailing assumption, we found that PGE(2) (0.1, 1, and 5 μmol/L) constricted rather than dilated parenchymal arterioles. Vasoconstriction to PGE(2) was prevented by inhibitors of EP(1) receptors. These results strongly argue against a direct role of PGE(2) on arterioles during neurovascular coupling.
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