N-Acetylcysteine for Preventing Pump-Induced Oxidoinflammatory Response During Cardiopulmonary Bypass |
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Authors: | Nehir Sucu Ismail Cinel Ali Unlu Barlas Aytacoglu LÜlÜfer Tamer Zeliha Kocak Kerem Karaca Ali Gul Murat Dikmengil UgĞur Atik Ugur Oral |
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Affiliation: | (1) Department of Cardiovascular Surgery, Mersin University, Medical School, Zeytinlibahce Cad., 33079, Mersin, Turkey;(2) Departments of Anesthesiology and Reanimation, Mersin University, Medical School, Zeytinlibahce Cad., 33079, Mersin, Turkey;(3) Department of Biochemistry, Mersin University, Medical School, Zeytinlibahce Cad., 33079, Mersin, Turkey |
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Abstract: | ![]() Purpose To investigate the effect of N-acetylcysteine on preventing pump-induced oxidoinflammatory response during cardiopulmonary bypass (CPB).Methods Forty patients undergoing coronary artery bypass grafting (CABG) were randomly divided into a study group (n = 20), given 50 mg kg–1 N-acetylcysteine intravenously for 3 days, and a control group (n = 20) given saline. Serum samples were collected for measurement of myeloperoxidase (MPO), malondialdehyde (MDA), interleukin-6, 1-acid glycoprotein (AAGP), and C-reactive protein (CRP) during surgery and postoperatively.Results The MPO and MDA values showed a similar pattern during and after CPB in the study group, with significantly less variance than in the control group. Interleukin-6 showed similar patterns in the two groups, but the data from 30 min after the start of CPB and from 6 h post-CPB were significantly different. The AAGP and CRP values were both elevated during CPB in the two groups without a significant difference, but 6 and 24 h post-CPB, the values were significantly higher in the control group than in the study group.Conclusions N-Acetylcysteine decreased pump-induced oxidoinflammatory response during CPB, suggesting that it could be a novel therapy for assisting in the prevention of CBP-induced oxidoinflammatory damage. |
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Keywords: | N-Acetylcysteine Cardiopulmonary by-pass Interleukin-6 Lipid peroxidation Myeloperoxidase Acute phase reactant |
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