Protective Effect of the Nuclear Factor Kappa B Inhibitor Pyrrolidine Dithiocarbamate in Lung Injury in Rats with Streptozotocin-Induced Diabetes

被引:26
作者
Eren, Gulay [2 ]
Cukurova, Zafer [2 ]
Hergunsel, Oya [2 ]
Demir, Guray [2 ]
Kucur, Mine [4 ]
Uslu, Ezel [4 ]
Dalo, Enis [4 ]
Uhri, Mehmet [3 ]
Tugcu, Volkan [1 ]
机构
[1] Bakirkoy Dr Sadi Konuk Training & Res Hosp, Dept Urol, TR-34147 Istanbul, Turkey
[2] Bakirkoy Dr Sadi Konuk Training & Res Hosp, Dept Anesthesiol & Intens Care, TR-34147 Istanbul, Turkey
[3] Bakirkoy Dr Sadi Konuk Training & Res Hosp, Dept Pathol, TR-34147 Istanbul, Turkey
[4] Istanbul Univ, Cerrahpasa Med Fac, Dept Biochem, Istanbul, Turkey
关键词
Diabetic complications; Lung injury; Oxidative stress; Nitric oxide synthase; endothelial; Nuclear factor kappa B; NITRIC-OXIDE SYNTHASE; OXIDATIVE PROTEIN DAMAGE; ALPHA-LIPOIC ACID; PYROLIDIUM DITHIOCARBAMATE; EPITHELIAL-CELLS; UP-REGULATION; STRESS; DISEASE; ACTIVATION; EXPRESSION;
D O I
10.1159/000264920
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Diabetes mellitus (DM) causes debilitating complications and, as a result, diabetics frequently require intensive care. Although lungs are not thought to be affected primarily by DM, an increasing number of studies indicate physiological and structural abnormalities in diabetic lungs. Objectives: Pyrrolidine dithiocarbamate (PDTC) is a metal chelator and a potent inhibitor of NF-kappa B. Keeping in mind that NF-kappa B activation may be crucial in end-organ injury due to DM, we studied the role of PDTC on the inhibition of NF-kappa B activation and its effects on possible lung injury in rats with streptozotocin-induced DM. Methods: 36 Sprague-Dawley rats were allocated into 4 groups: diabetes, diabetes + PDTC, control and control + PDTC. At the end of 10 weeks, rats were sacrificed and their lungs were taken for histopathological and immunohistochemical evaluation [for NF-kappa B (p65) and endothelial nitric oxide (eNOS) immunoreactivities]. Protein carbonyl content (PCC), superoxide dismutase (SOD) and reduced glutathione (GSH) activities were measured. Results: Histopathologically, basal membranes were thickened and there was intense inflammatory reaction in diabetic lungs. However, the PDTC group, in which there were poor positive expressions of eNOS and p65 activity compared to diabetes group, revealed fewer inflammatory changes. PCC levels in diabetic lungs were higher, but SOD and GSH activities were lower. However, measurements of these parameters in the PDTC group and controls gave similar results. Conclusion: Lungs are exposed to changes induced by oxidative stress in diabetes through NF-kappa B activation and PDTC seems to be useful to prevent diabetic lung injury. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:402 / 410
页数:9
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