Cardiovascular diseases involve changes in the structure of the heart
and blood vessels. Normal structure is maintained by a sophisticated s
et of mechanical and cellular ''checks and balances.'' A disturbance o
f these checks and balances induces a remodeling process. The most dis
tinguished features of this process are phenotypic modulation of vario
us cell types in the cardiovascular system; cellular hyperplasia and h
ypertrophy; and extracellular matrix production, deposition, and degra
dation. Optimal pharmacotherapy of cardiovascular diseases should be a
imed at correcting structural abnormalities in the heart and blood ves
sels. This goal can be achieved by influencing mechanical stresses on
the cardiovascular system or by interfering with the chemical mediator
s of the remodeling process. Many existing groups of cardiovascular dr
ugs, such as angiotensin-converting enzyme inhibitors, calcium-antagon
ists, alpha- and beta-adrenoceptor antagonists, and antithrombotic dru
gs, influence cardiovascular remodeling. New approaches involve the de
velopment of drugs acting on peptidergic mediators of cardiovascular r
emodeling.