HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Thromboxane receptor blockade improves the antiatherogenic effect of thromboxane A2 suppression in LDLR KO mice.

Abstract
Suppression of thromboxane (Tx) A(2) biosynthesis retards atherogenesis. In this setting, the coincidental presence of nonconventional ligands for the TxA(2) receptor (TP), such as isoprostanes, could still induce a proatherogenic vascular phenotype. However, no data are available on the effect of combining suppression of TxA(2) formation with blockade of TP in atherogenesis. To this end, we tested the effect of a selective COX-1 inhibitor, SC560, a TP antagonist, BM-573, or a combination of both in low-density lipoprotein receptor-deficient mice on a high-fat diet. None of the treatments affected body weight or plasma cholesterol or triglycerides levels. Although SC-560 suppressed TxA(2) biosynthesis, BM-573 reduced its levels by 35%; in contrast, the 2 drugs, alone or in combination, did not significantly affect prostacyclin levels. At the end of the study, SC560 and BM-573 reduced atherogenesis; however, a further significant decrease was observed in mice receiving both drugs. This effect was associated with a further significant reduction of vascular inflammation, a decrease in macrophages, and an increase in the content of collagen and smooth muscle cells of the atherosclerotic lesions. These results show for the first time that the addition of a TP antagonist increases the antiatherogenic effect of COX-1-dependent TxA(2) suppression.
AuthorsTillmann Cyrus, Yuemang Yao, Tao Ding, Jean Michel Dogné, Domenico Praticò
JournalBlood (Blood) Vol. 109 Issue 8 Pg. 3291-6 (Apr 15 2007) ISSN: 0006-4971 [Print] United States
PMID17158227 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Membrane Proteins
  • N-terbutyl-N'-(2-(4'-methylphenylamino)-5-nitrobenzenesulfonyl)urea
  • Pyrazoles
  • Receptors, LDL
  • Receptors, Thromboxane A2, Prostaglandin H2
  • SC 560
  • Sulfonylurea Compounds
  • Triglycerides
  • Thromboxane A2
  • Collagen
  • Cholesterol
  • Epoprostenol
  • Cyclooxygenase 1
  • Ptgs1 protein, mouse
Topics
  • Animals
  • Atherosclerosis (blood, drug therapy)
  • Cholesterol (blood)
  • Collagen (metabolism)
  • Cyclooxygenase 1 (metabolism)
  • Epoprostenol (metabolism)
  • Macrophages (metabolism)
  • Membrane Proteins (antagonists & inhibitors, metabolism)
  • Mice
  • Mice, Knockout
  • Myocytes, Smooth Muscle (metabolism)
  • Pyrazoles (pharmacology)
  • Receptors, LDL (deficiency)
  • Receptors, Thromboxane A2, Prostaglandin H2 (antagonists & inhibitors)
  • Sulfonylurea Compounds (pharmacology)
  • Thromboxane A2 (metabolism)
  • Triglycerides (blood)
  • Vasculitis (blood, drug therapy)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: