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胞磷胆碱对三硝基苯磺酸诱导的大鼠实验性结肠炎的保护作用。

Protective effects of citicoline on TNBS-induced experimental colitis in rats.

作者信息

Ek Rauf Onur, Serter Mukadder, Ergin Kemal, Cecen Serpil, Unsal Cengiz, Yildiz Yuksel, Bilgin Mehmet D

机构信息

Department of Physiology, Adnan Menderes University Aydin, Turkey.

Department of Biochemistry, Adnan Menderes University Aydin, Turkey.

出版信息

Int J Clin Exp Med. 2014 Apr 15;7(4):989-97. eCollection 2014.

PMID:24955172
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4057851/
Abstract

The aim of this study was to investigate the effects of citicoline on the development of colitis and antioxidant parameters in rats subjected to tribenzene sulfonic acid (TNBS)-induced colitis. Twenty four Wistar Albino female rats were divided into four subgroups (n=6) (control, colitis control, colitis + 50 mg/kg citicoline, colitis + 250 mg/kg citicoline). Colitis was induced using an enema of TNBS and ethanol; following which citicoline was administrated for 3 days and effects of citicoline was subsequently evaluated. Based on microscopic damage scores, there was no difference between rats of the TNBS-colitis and 50 mg/kg citicoline treated groups, whereas treatment with 250 mg/kg citicoline, caused significant reduction in colon injury compared to that observed in rats of TNBS-colitis group. In terms of the biochemical analyses, myeloperoxidase (MPO), malondialdehyde (MDA), reduced glutathione (GSH), and IL-6 levels in rats from 250 mg/kg citicoline group were significantly different from that TNBS-colitis group. The levels of MPO, MDA, GSH and IL-6 in control rats were also significantly different those of rats in the TNBS-colitis group. Citicoline may have a positive protective effect on the inflammatory bowel disease treatment process and could, therefore, be used as an adjunct therapy in colitis. These effects of citicoline may exist through anti-inflammatory and antioxidant mechanism.

摘要

本研究旨在探讨胞磷胆碱对三硝基苯磺酸(TNBS)诱导的大鼠结肠炎发展及抗氧化参数的影响。将24只Wistar白化雌性大鼠分为四个亚组(n = 6)(对照组、结肠炎对照组、结肠炎 + 50 mg/kg胞磷胆碱组、结肠炎 + 250 mg/kg胞磷胆碱组)。使用TNBS和乙醇灌肠诱导结肠炎;随后给予胞磷胆碱3天,并评估胞磷胆碱的效果。根据显微镜损伤评分,TNBS结肠炎组和50 mg/kg胞磷胆碱治疗组的大鼠之间没有差异,而与TNBS结肠炎组大鼠相比,250 mg/kg胞磷胆碱治疗导致结肠损伤显著减轻。在生化分析方面,250 mg/kg胞磷胆碱组大鼠的髓过氧化物酶(MPO)、丙二醛(MDA)、还原型谷胱甘肽(GSH)和白细胞介素-6水平与TNBS结肠炎组有显著差异。对照组大鼠的MPO、MDA、GSH和IL-6水平与TNBS结肠炎组大鼠也有显著差异。胞磷胆碱可能对炎症性肠病治疗过程具有积极的保护作用,因此可作为结肠炎的辅助治疗药物。胞磷胆碱的这些作用可能通过抗炎和抗氧化机制存在。

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