EP2 Receptor Blockade Attenuates COX-2 Upregulation During Intestinal Inflammation.
Journal
Shock (Augusta, Ga.)
ISSN: 1540-0514
Titre abrégé: Shock
Pays: United States
ID NLM: 9421564
Informations de publication
Date de publication:
09 2020
09 2020
Historique:
pubmed:
7
9
2019
medline:
20
7
2021
entrez:
7
9
2019
Statut:
ppublish
Résumé
High levels of PGE2 have been implicated in the pathogenesis of intestinal inflammatory disorders such as necrotizing enterocolitis (NEC) and peritonitis. However, PGE2 has a paradoxical effect: its low levels promote intestinal homeostasis, whereas high levels may contribute to pathology. These concentration-dependent effects are mediated by four receptors, EP1-EP4. In this study, we evaluate the effect of blockade of the low affinity pro-inflammatory receptors EP1 and EP2 on expression of COX-2, the rate-limiting enzyme in PGE2 biosynthesis, and on gut barrier permeability using cultured enterocytes and three different models of intestinal injury. PGE2 upregulated COX-2 in IEC-6 enterocytes, and this response was blocked by the EP2 antagonist PF-04418948, but not by the EP1 antagonist ONO-8711 or EP4 antagonist E7046. In the neonatal rat model of NEC, EP2 antagonist and low dose of COX-2 inhibitor Celecoxib, but not EP1 antagonist, reduced NEC pathology as well as COX-2 mRNA and protein expression. In the adult mouse endotoxemia and cecal ligation/puncture models, EP2, but not EP1 genetic deficiency decreased COX-2 expression in the intestine. Our results indicate that the EP2 receptor plays a critical role in the positive feedback regulation of intestinal COX-2 by its end-product PGE2 during inflammation and may be a novel therapeutic target in the treatment of NEC.
Identifiants
pubmed: 31490357
doi: 10.1097/SHK.0000000000001444
pmc: PMC7051888
mid: NIHMS1538385
pii: 00024382-202009000-00016
doi:
Substances chimiques
Cyclooxygenase 2
EC 1.14.99.1
Dinoprostone
K7Q1JQR04M
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
394-401Subventions
Organisme : NIAID NIH HHS
ID : R01 AI014032
Pays : United States
Références
J Exp Med. 2009 Mar 16;206(3):535-48
pubmed: 19273625
Eur J Pharmacol. 2013 Oct 15;718(1-3):408-17
pubmed: 23973650
Dig Dis Sci. 2002 Apr;47(4):894-904
pubmed: 11991626
Am J Kidney Dis. 2001 Dec;38(6):1145-57
pubmed: 11728945
Trends Pharmacol Sci. 2013 Jul;34(7):413-23
pubmed: 23796953
Prostaglandins Other Lipid Mediat. 2002 Aug;68-69:177-85
pubmed: 12432917
J Med Chem. 2014 Jun 12;57(11):4454-65
pubmed: 24279689
Carcinogenesis. 2007 Oct;28(10):2063-8
pubmed: 17277233
Lab Invest. 2013 Dec;93(12):1265-75
pubmed: 24126890
Crit Care Clin. 2016 Apr;32(2):203-12
pubmed: 27016162
Prostaglandins Other Lipid Mediat. 2002 Aug;68-69:557-73
pubmed: 12432943
Surg Clin North Am. 2014 Dec;94(6):1151-61
pubmed: 25440116
Mol Med Rep. 2015 Jun;11(6):4454-62
pubmed: 25625500
Cleve Clin J Med. 2002;69 Suppl 1:SI47-52
pubmed: 12086293
Med Clin North Am. 1994 Nov;78(6):1207-31
pubmed: 7967905
J Biol Chem. 2001 Aug 24;276(34):31720-31
pubmed: 11423555
J Pediatr Surg. 2007 Jul;42(7):1165-71
pubmed: 17618875
Int Immunopharmacol. 2014 Oct;22(2):311-7
pubmed: 25063710
J Surg Res. 2000 Jul;92(1):71-7
pubmed: 10864485
J Pediatr Surg. 2013 Nov;48(11):2301-7
pubmed: 24210203
Eur J Pharmacol. 2017 Feb 5;796:7-19
pubmed: 27940058
Adv Exp Med Biol. 1997;407:163-70
pubmed: 9321948
Br J Pharmacol. 2006 Nov;149(6):611-23
pubmed: 17016496
Biochem Biophys Res Commun. 2000 Jun 16;272(3):744-8
pubmed: 10860826
Cancer Res. 2015 Jul 15;75(14):2822-32
pubmed: 26018088
J Inflamm Res. 2015 Oct 16;8:201-9
pubmed: 26527892
Arthritis Rheum. 2007 Aug;56(8):2608-19
pubmed: 17665454
J Immunol. 2011 Nov 15;187(10):5255-67
pubmed: 21967897
Shock. 2000 Sep;14(3):374-9
pubmed: 11028559
Shock. 2000 Feb;13(2):110-6
pubmed: 10670840