| First Author | Liu B | Year | 2019 |
| Journal | FASEB J | Volume | 33 |
| Issue | 2 | Pages | 2451-2459 |
| PubMed ID | 30277822 | Mgi Jnum | J:286675 |
| Mgi Id | MGI:6388225 | Doi | 10.1096/fj.201801064RR |
| Citation | Liu B, et al. (2019) TP and/or EP3 receptors mediate the vasoconstrictor and pressor responses of prostaglandin F2alpha in mice and/or humans. FASEB J 33(2):2451-2459 |
| abstractText | The vasoconstrictor and/or pressor effects of prostaglandin (PG)F2alpha participate in the development of vascular pathologies and limit the clinical use of the agent. This study aimed to determine the receptor types responsible for the vasoconstrictor activity of PGF2alpha and whether they mediate the pressor response evoked by the prostanoid under in vivo conditions. Experiments were performed on genetically altered mice and/or on vessels from these mice or humans. Here we show that deletion of the thromboxane-prostanoid receptor (TP(-/-)) abolished or drastically diminished the contraction to PGF2alpha in isolated mouse vessels (some of which were resistance arteries) and reduced the elevation in blood pressure evoked by the prostanoid under in vivo conditions. In accordance, TP antagonism abolished the contraction in small arteries of human omentum. Further deletion of E prostanoid receptor type 3 (EP3(-/-)) removed the PGF2alpha-evoked contraction that remained in some TP(-/-) arteries and added to the effect of TP(-/-) on the elevation in blood pressure evoked by the prostanoid under in vivo conditions. In contrast, the uterine contraction to PGF2alpha mediated via the F prostanoid receptor (FP) was unaltered in TP(-/-)/EP3(-/-) mice. These results demonstrate that the non-FP receptors TP and/or EP3 mediate the vasoconstrictor and pressor effects of PGF2alpha, which are still of concern under clinical conditions.-Liu, B., Li, J., Yan, H., Tian, D., Li, H., Zhang, Y., Guo, T., Wu, X., Luo, W., Zhou, Y. TP and/or EP3 receptors mediate the vasoconstrictor and pressor responses of prostaglandin F2alpha in mice and/or humans. |
