Role of Transforming Growth Factor-β1 in Cardiovascular Inflammatory Changes Induced by Chronic Inhibition of Nitric Oxide Synthesis

Publisher Website
Google Scholar
Abstract
Abstract —We previously reported that chronic inhibition of nitric oxide (NO) synthesis with N ω -nitro- l -arginine methyl ester (L-NAME) induces inflammatory changes (monocyte infiltration, myofibroblast formation, and monocyte chemoattractant protein-1 [MCP-1] and transforming growth factor-β1 [TGF-β1] expression) in the rat heart and vessel. There is debate regarding whether TGF-β1 exhibits proinflammatory or anti-inflammatory activities. We used the rat model to investigate the role of TGF-β in the pathogenesis of such inflammatory changes. We show here that infiltrating monocytes and myofibroblasts in the inflammatory lesions produced TGF-β1 on the third day of L-NAME administration. Cotreatment with a monoclonal antibody against TGF-β1, but not with control IgG, prevented the L-NAME–induced cardiac inflammation. The antibody also significantly inhibited the gene expression of MCP-1, P-selectin, and intercellular adhesion molecule-1. In summary, the antibody against TGF-β1 prevented inflammatory changes in rat heart and vessel induced by chronic inhibition of NO synthesis, suggesting that increased production of TGF-β1 is involved in the inflammatory changes in this model.

This publication has 14 references indexed in Scilit: