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High Levels of Circulating Epinephrine Trigger Apical Cardiodepression in a β 2 -Adrenergic Receptor/G i –Dependent Manner
Author(s) -
Helen Paur,
Peter Wright,
Markus B. Sikkel,
Matthew H. Tranter,
Catherine Mansfield,
Peter O’Gara,
Daniel J. Stuckey,
Viacheslav O. Nikolaev,
Ivan Diakonov,
Laura Pannell,
HaiBin Gong,
Hong Sun,
Nicholas S. Peters,
Mario Petrou,
Zhaolun Zheng,
Julia Gorelik,
Alexander R. Lyon,
Siân E. Harding
Publication year - 2012
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.112.111591
Subject(s) - medicine , epinephrine , adrenergic receptor , adrenergic , endocrinology , receptor , β2 adrenergic receptor , agonist
Takotsubo cardiomyopathy is an acute heart failure syndrome characterized by myocardial hypocontractility from the mid left ventricle to the apex. It is precipitated by extreme stress and can be triggered by intravenous catecholamine administration, particularly epinephrine. Despite its grave presentation, Takotsubo cardiomyopathy is rapidly reversible, with generally good prognosis. We hypothesized that this represents switching of epinephrine signaling through the pleiotropic β(2)-adrenergic receptor (β(2)AR) from canonical stimulatory G-protein-activated cardiostimulant to inhibitory G-protein-activated cardiodepressant pathways.

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