Gender differences in non-ischemic myocardial remodeling: are they due to estrogen modulation of cardiac mast cells and/or membrane type 1 matrix metalloproteinase. Pflugers Arch 2013 May;465(5):687-97
Date
02/19/2013Pubmed ID
23417570Pubmed Central ID
PMC3654075DOI
10.1007/s00424-013-1229-9Scopus ID
2-s2.0-84878016359 (requires institutional sign-in at Scopus site) 14 CitationsAbstract
This review is focused on gender differences in cardiac remodeling secondary to sustained increases in cardiac volume (VO) and generated pressure (PO). Estrogen has been shown to favorably alter the course of VO-induced remodeling. That is, the VO-induced increased extracellular matrix proteolytic activity and mast cell degranulation responsible for the adverse cardiac remodeling in males and ovariectomized rodents do not occur in intact premenopausal females. While less is known regarding the mechanisms responsible for female cardioprotection in PO-induced stress, gender differences in remodeling have been reported indicating the ability of premenopausal females to adequately compensate. In view of the fact that, in male mice with PO, mast cells have been shown to play a role in the adverse remodeling suggests favorable estrogen modification of mast cell phenotype may also be responsible for cardioprotection in females with PO. Thus, while evidence is accumulating regarding premenopausal females being cardioprotected, there remains the need for in-depth studies to identify critical downstream molecular targets that are under the regulation of estrogen and relevant to cardiac remodeling. Such studies would result in the development of therapy which provides cardioprotection while avoiding the adverse effects of systemic estrogen delivery.
Author List
Janicki JS, Spinale FG, Levick SPMESH terms used to index this publication - Major topics in bold
AnimalsEstrogens
Female
Humans
Male
Mast Cells
Matrix Metalloproteinase 14
Mice
Myocardium
Sex Characteristics
Ventricular Remodeling
