:: Volume 18, Issue 1 (1-2014) ::
IBJ 2014, 18(1): 23-27 Back to browse issues page
Pentoxifylline Decreases Serum Level of Adhesion Molecules in Atherosclerosis Patients
Amir Hooshang Mohammadpour , Homa Falsoleiman , Jamal Shamsara , Ghazaleh Allah Abadi , Ramin Rasooli , Mohammad Ramezani
Background: Inflammation is involved in development, progression, and complications of atherosclerotic disease. Clinical studies have indicated that the level of monocyte chemoattractant protein 1 (MCP-1), IL-18, and adhesion molecules correlates with the severity of atherosclerosis and can predict future cardiovascular events. Experimental studies have shown pentoxifylline (PTX) reduces these factors in animal models. The purpose of the present pilot study was to evaluate effect of PTX on a group of inflammatory biomarkers in patients with coronary artery disease (CAD). Methods: Forty patients with angiographically documented CAD, who fulfilled inclusion and exclusion criteria, were entered in the double-blind, randomized, pilot clinical study. The patients were randomly given PTX (400 mg three times daily) or placebo (3 tab/day) for 2 months. Serum concentrations of MCP-1, IL-18, intercellular adhesion Molecule 1 (ICAM-1), and vascular cell adhesion molecule 1 (VCAM-1) were measured before and at the end of intervention by enzyme-linked immunosorbant assay. Results: Our study showed that the serum levels of ICAM-1 and VCAM-1 was decreased in the study population after two-month treatment (P<0.05). Conclusion: Based on the results of our pilot study, administration of PTX in CAD patients significantly decreases adhesion molecules levels.
Keywords: Atherosclerosis, Inflammation, Pentoxifylline
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Type of Study: Full Length | Subject: Related Fields
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Mohammadpour A H, Falsoleiman H, Shamsara J, Allah Abadi G, Rasooli R, Ramezani M. Pentoxifylline Decreases Serum Level of Adhesion Molecules in Atherosclerosis Patients. IBJ. 2014; 18 (1) :23-27
URL: http://ibj.pasteur.ac.ir/article-1-1026-en.html

Volume 18, Issue 1 (1-2014) Back to browse issues page
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