Prostaglandin E2, a postulated astrocyte-derived neurovascular coupling agent, constricts rather than dilates parenchymal arterioles

J Cereb Blood Flow Metab. 2013 Apr;33(4):479-82. doi: 10.1038/jcbfm.2013.9. Epub 2013 Feb 6.

Abstract

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arterioles / metabolism
  • Astrocytes / metabolism*
  • Brain / blood supply*
  • Brain / metabolism
  • Cerebrovascular Circulation / physiology*
  • Dinoprostone / metabolism*
  • Male
  • Mice
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Prostaglandin E, EP1 Subtype / metabolism
  • Vasoconstriction / physiology*

Substances

  • Receptors, Prostaglandin E, EP1 Subtype
  • Dinoprostone