4.7 Article

Role of Prostaglandins in Nitric Oxide-Induced Glial Cell-Mediated Vasodilation in Rat Retina

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BIOMOLECULES
卷 12, 期 10, 页码 -

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MDPI
DOI: 10.3390/biom12101403

关键词

glial cell; nitric oxide; prostanoid EP2 receptor; retina

资金

  1. Ministry of Education, Culture, Sports, Science, and Technology of Japan [18K06704]

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This study finds that NO-induced neuronal cell action on glial cells causes vasodilation in the rat retina through the activation of prostanoid EP2 receptors via the arachidonic acid cascade. Glial cell-derived PGE(2) may play an important role in retinal vasodilatory mechanisms.
We previously identified that NO derived from neuronal cells acts on glial cells and causes vasodilation in the healthy rat retina via the release of epoxyeicosatrienoic acids (EETs) and prostaglandins (PGs) by activation of the arachidonic acid cascade. However, it is not clear which PG types are involved in these responses. The aim of the present study was to identify prostanoid receptors involved in glial cell-derived vasodilation induced by NO in rat retina. Male Wistar rats were used to examine the effects of intravitreal pretreatment with indomethacin, a cyclooxygenase inhibitor; PF-04418948, a prostanoid EP2 receptor antagonist; and CAY10441, a prostanoid IP receptor antagonist, on the changes in the retinal arteriolar diameter induced by intravitreal administration of NOR3, an NO donor. Retinal arteriolar diameters were measured using ocular fundus images captured with a high-resolution digital camera in vivo. The increase in the retinal arteriolar diameter induced by intravitreal injection of NOR3 was significantly suppressed by intravitreal pretreatment with indomethacin and PF-04418948, but not by CAY10441. The dose of PF-04418948 and CAY10441 injected intravitreally in the present study significantly reduced the increase in the retinal arteriolar diameter induced by prostaglandin E-2 (PGE(2)) and prostaglandin I-2 (PGI(2)), respectively. These results suggest that activation of the arachidonic acid cascade and subsequent stimulation of prostanoid EP2 receptors are involved in rat retinal vasodilatory responses evoked by NO-induced glial cell stimulation. Therefore, glial cell-derived PGE(2), similar to EETs, may play an important role in retinal vasodilatory mechanisms.

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