Angiotensin II receptor antagonists Angiotensin II receptor antagonists (ARBs) have very similar effects to angiotensin converting enzyme inhibitors and are used for the same indications (hypertension, heart failure, post-myocardial infarction). Their mechanism of action, however, is very different. ARBs are receptor antagonists that

block type 1 angiotensin II (AT1) receptors on blood vessels and other tissues Inhibitors,research,lifescience,medical such as the heart. ARBs are primarily used where patients are intolerant of ACE inhibitor therapy. They do not inhibit the breakdown of bradykinin or other kinins, and are thus only rarely associated with persistent dry cough and/or angioedema, that limit ACEi therapy.

More recently they have been used for the treatment of heart failure. Losartan, irbesartan, olmesartan, candesartan, valsartan and telmisartan are included in this group of drugs. Losartan Two papers (22, 23) have recently been published Inhibitors,research,lifescience,medical stressing as chronic losartan administration is able to preserve or www.selleckchem.com/products/Enzastaurin.html improve cardiac function in dystrophin-deficient mdx mice, by a decrease of cardiac and skeletal muscle fibrosis. Nevertheless Inhibitors,research,lifescience,medical no impact on the skeletal muscle disease progression was observed, suggesting that other pathways that trigger fibrosis dominate over angiotensin II in skeletal muscle long term, unlike the situation in the heart. These studies suggest that ARBs may be an important prophylactic treatment for DMD-associated cardiomyopathy, but they will not impact

skeletal muscle disease. Beta-blockers Beta-blockers are drugs that bind to beta-adrenoceptors Inhibitors,research,lifescience,medical and thereby block the binding of norepinephrine and epinephrine to these receptors, with consequent inhibition of normal sympathetic effects that act through these receptors. Therefore, beta-blockers are sympatholytic drugs. The first generation of beta-blockers were non-selective, Inhibitors,research,lifescience,medical meaning that they blocked both beta-1 (β1) and beta-2 (β2) adrenoceptors. Second generation beta-blockers are more cardioselective in that they are relatively Cilengitide selective for β1 adrenoceptors. Beta-blockers bind to beta-adrenoceptors located in cardiac nodal tissue, the conducting system, and contracting myocytes. The heart has both β1 and β2 adrenoceptors, although the predominant receptor type in number and function is β1. Beta-blockers are able to reduce sympathetic influences that normally stimulate chronotropy (heart rate), inotropy (contractility), dromotropy (electrical conduction) and lusitropy (relaxation). Therefore, beta-blockers cause decreases in heart rate, contractility, screening library conduction velocity, and relaxation rate.