Atenolol is a  1 -selective drug, which exerts greater blocking activity on  1 -adrenoreceptors than on  2 -adrenoreceptors, with the S-enantiomer being more active than R-enantiomer. The aim of this study was to investigate the proteins with differential protein expression levels in the proteome of vascular smooth muscle cells (A7r5) incubated separately with individual enantiomers of atenolol using an iTRAQ-coupled two-dimensional LC-MS/MS approach. Our results indicated that some calcium-binding proteins such as calmodulin, protein S100-A11, protein S100-A4, and annexin A6 were downregulated and showed relatively lower protein levels in cells incubated with the S-enantiomer of atenolol than those incubated with the R-enantiomer, whereas metabolic enzymes such as aspartate aminotransferase, glutathione S-transferase P, NADH-cytochrome b 5 reductase, and ␣-N-acetylgalactosaminidase precursor were up-regulated and displayed higher protein levels in cells incubated with the S-enantiomer relative to those incubated with the R-enantiomer. The involvement of NADHcytochrome b 5 reductase in the intracellular anabolic activity was validated by NAD ؉ /NADH assay with a higher ratio of NAD ؉ /NADH correlating with a higher proportion of NAD ؉ . The down-regulation of the calciumbinding proteins was possibly involved in the lower intracellular Ca 2؉ The -adrenoreceptors belong to the family of G proteincoupled receptors (GPRs) 1 (1) characterized by seven transmembrane-spanning domains forming a pocket in which the agonists and competitive antagonists find their binding sites (2). The signal transduction process triggered by agonist binding to -adrenoreceptors consists of discrete steps, and one of the earliest is the coupling of this complex to heterotrimeric G protein that dissociates in G␣ and G␥ subunits (3). G␣ and G␥ subunits activate or inhibit a number of effector enzymes such as adenylyl cyclase, phospholipase C, ion channels, or mitogen-activated protein kinases (MAPKs), resulting in a variety of cellular functions. One of the well documented signal transduction steps is that the coupling of this complex to the heterotrimeric G protein G␣ subunits will stimulate adenylyl cyclase activity, which produces the second messenger cAMP. Protein kinase A activated by cAMP phosphorylates L-type calcium channels and myosin light chain kinase (4, 5), facilitating Ca 2ϩ entry and producing the positive inotropic effect in atria and ventricles. In addition to mechanisms that indirectly lead to alterations in ion transport, -adrenoreceptor activation is more directly linked to ion channels (6). After agonist stimulation, most GPRs rapidly lose their ability to respond to agonist. For many GPRs, this process, commonly referred to as desensitization, appears to be primarily mediated by two protein families: G protein-coupled receptor kinases (GRKs) and arrestins. GRKs specifically bind to the agonist-occupied receptor, thereby promoting receptor phosphorylation, which in turn leads to arrestin binding. Arrestin bin...