Title : PGE2-EP3 signaling exacerbates intracerebral hemorrhage outcomes in 24-mo-old mice.

Pub. Date : 2016 Jun 1

PMID : 27084388






4 Functional Relationships(s)
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1 PGE2-EP3 signaling exacerbates intracerebral hemorrhage outcomes in 24-mo-old mice. Dinoprostone prostaglandin E receptor 3 (subtype EP3) Mus musculus
2 EP3 is the most abundant EP receptor in the brain and we have previously shown that signaling through the PGE2-EP3 axis exacerbates ICH outcomes in young mice. Dinoprostone prostaglandin E receptor 3 (subtype EP3) Mus musculus
3 EP3 is the most abundant EP receptor in the brain and we have previously shown that signaling through the PGE2-EP3 axis exacerbates ICH outcomes in young mice. Dinoprostone prostaglandin E receptor 3 (subtype EP3) Mus musculus
4 Using this aged cohort of mice, we have confirmed and extended our previous results in young mice demonstrating the deleterious role of the PGE2-EP3 signaling axis in modulating brain injury and functional recovery after ICH, further supporting the notion of the EP3 receptor as a putative therapeutic avenue for the treatment of ICH. Dinoprostone prostaglandin E receptor 3 (subtype EP3) Mus musculus