Mechanical stress induces cardiac hypertrophy through mechanisms involving vasoactive peptides, CaMK, and calcineurin, which play critical roles in hypertrophic responses.
Congestive heart failure is one of the major issues for cardiologists. Since cardiac hypertrophy deteriorates into heart failure, it is important to elucidate the mechanisms of cardiac hypertrophy. Hemodynamic overload, namely mechanical stress, is a major cause for cardiac hypertrophy. Mechanical stress induces various hypertrophic responses such as activation of phosphorylation cascades of many protein kinases, expression of specific genes and an increase in protein synthesis. During this process, secretion and production of vasoactive peptides such as angiotensin II and endothelin-1, are increased and play critical roles in the induction of these hypertrophic responses. Recently, a Ca2+ dependent protein kinase, CaMK, and a Ca2+ dependent protein phosphatase, calcineurin, have attracted great attention as critical molecules that induce cardiac hypertrophy. In this review, we described the mechanisms by which mechanical stress induces cardiac hypertrophy, especially focusing on the role of calcineurin in the development of cardiac hypertrophy.
Zou et al. (Tue,) conducted a review in Cardiac hypertrophy. Mechanical stress induces cardiac hypertrophy through mechanisms involving vasoactive peptides, CaMK, and calcineurin, which play critical roles in hypertrophic responses.