Carvedilol is a vasodilating, beta-adrenoceptor antagonist currently marketed for the treatment of mild to moderate hypertension. Carvedilol acts to reduce total peripheral resistance by blocking peripheral vascular alpha(1)-adrenoceptors, thereby producing systemic arterial vasodilation, while at the same time inhibiting reflex tachycardia through the blockade of myocardial beta-adrenoceptors. In addition to its established efficacy and safety as an antihypertensive agent, carvedilol has been shown to produce significant cardioprotection in experimental animal models of acute myocardial infarction, with the most dramatic effect being observed in the pig model of myocardial ischaemia and reperfusion, where the reduction in infarct size reached 91%. Recent pharmacological studies have revealed additional novel properties of carvedilol which may account for the marked protection produced by the drug in the ischaemic myocardium and which may also result in protection against other chronic pathological processes, such as atherosclerosis and acute vascular injuries. The latter arise from surgical procedures, such as percutaneous transluminal coronary angioplasty and coronary artery bypass grafting. Specifically, carvenilol, as well as some of its hydroxylated metabolites, are potent antioxidants. In physicochemical, biochemical and cellular assays carvedilol and several of its metabolites prevent lipid peroxidation and the depletion of endogenous antioxidants, such as vitamin E and glutathione. Moreover, carvedilol and its metabolites prevent the oxidation of LDL to oxidized LDL, the latter being directly cytotoxic and known to activate monocytes/macrophages and to stimulate foam cell formation. In addition, carvedilol was found to inhibit both rat and human vascular smooth muscle cell proliferation and migration. The ability of carvedilol to inhibit vascular smooth muscle proliferation was observed against a wide variety of mitogens (e.g. PDGF FGF ET-I, th ombin, serum), indicating that the sire of inhibition is likely to be through some final common pathway beyond the specific mitogen receptors. Likewise, carvedilol inhibited vascular smooth muscle cell migration to multiple chemoattractants, including PDGF and osteopontin. The significance of these activities of carvedilol to inhibit vascular smooth muscle cell migration and proliferation, which have been demonstrated in vitro were also investigated in vivo in a rat model of neointima formation following acute carotid artery injury by balloon angioplasty. In this model carvedilol inhibited, by 85%, the growth of neointima resulting from the vascular injury, and did so at a dosage that is similar To that used in humans for the treatment of angina. Taken together these results indicate that carvedilol is a unique multiple action antilhypertensive drug which not only normalizes blood pressure, but may also provide protection for the major organs of the cardiovascular system, and in particular the heart and vasculature.
