Genetic and Pharmacological Manipulation of Urotensin II Ameliorate the Metabolic and Atherosclerosis Sequalae in Mice
Author(s) -
Zhipeng You,
Jacques Genest,
Pierre-Olivier Barrette,
Anouar Hafiane,
David J. Behm,
Pedro D’Orléans-Juste,
Adel Schwertani
Publication year - 2012
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.112.252973
Subject(s) - urotensin ii , hyperlipidemia , endocrinology , medicine , knockout mouse , apolipoprotein b , receptor , ldl receptor , lipoprotein , biology , cholesterol , diabetes mellitus
Urotensin II (UII) is a potent vasoactive peptide that binds to the urotensin receptor-coupled receptor-14 (known as UT) and exerts a wide range of actions in humans and experimental animals. We tested the hypothesis that UII gene deletion or UT blockade ameliorate experimental atherosclerosis.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom