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香烟烟雾和乙醇摄入对膳食缺锌和脱氧胆酸补充诱导的小鼠食管黏膜变化的影响。

Effects of cigarette smoke and ethanol intake on mouse oesophageal mucosa changes induced by dietary zinc deficiency and deoxycholic acid supplementation.

机构信息

Department of Morphology, Institute of Biosciences, UNESP, São Paulo State University, Botucatu, SP, Brazil.

出版信息

Basic Clin Pharmacol Toxicol. 2012 Aug;111(2):92-8. doi: 10.1111/j.1742-7843.2012.00867.x. Epub 2012 Mar 10.

Abstract

The noxious effects of dietary zinc deficiency (ZD) and deoxycholic bile acid (DCA) supplementation in the oesophagus were investigated. The additional influence of cigarette smoke and ethanol intake on the changes in the oesophageal mucosa induced by dietary ZD plus DCA was also assessed. Male C57BL/6 mice were allocated into four groups: Group 1 was fed control diet and groups 2-4 were fed ZD plus DCA diet. After 5 weeks, groups 3 and 4 were exposed to 10% ethanol intake or cigarette smoke for 15 weeks, respectively. All animals were euthanized at the end of week 20, and the oesophagus, lung, liver and colon were collected and analysed by conventional morphology. Cell proliferation was assessed in the oesophageal mucosa by Ki-67 immunohistochemistry and cyclooxygenase 2 (COX-2) protein by Western blotting. Dietary ZD plus DCA treatment induced mild hyperkeratosis and hyperplasia, increased cell proliferation index and COX-2 protein expression in the oesophagus, and intranuclear inclusion, karyocytomegaly and microvesicular fatty change in the liver. Cigarette smoke increased COX-2 protein expression in oesophageal mucosa and irregular enlargement of alveolus and alveolar ductal air spaces, while ethanol enhanced liver damage induced by ZD plus DCA diet. These findings indicate that dietary ZD plus DCA treatment during 20 weeks induces a pattern of chemical oesophageal injury but not Barrett's-like lesions.

摘要

研究了饮食性缺锌(ZD)和脱氧胆酸(DCA)补充对食管的有害影响。还评估了香烟烟雾和乙醇摄入对饮食性 ZD 加 DCA 引起的食管黏膜变化的额外影响。雄性 C57BL/6 小鼠被分为四组:第 1 组喂食对照饮食,第 2-4 组喂食 ZD 加 DCA 饮食。5 周后,第 3 和第 4 组分别暴露于 10%乙醇摄入或香烟烟雾 15 周。所有动物在第 20 周结束时被安乐死,收集和分析食管、肺、肝和结肠进行常规形态学分析。通过 Ki-67 免疫组化评估食管黏膜细胞增殖,通过 Western blot 评估环氧化酶 2(COX-2)蛋白。饮食性 ZD 加 DCA 处理诱导食管轻度角化过度和增生,增加细胞增殖指数和 COX-2 蛋白表达,以及肝细胞核内包涵体、核肥大和微泡脂肪变性。香烟烟雾增加食管黏膜 COX-2 蛋白表达和肺泡不规则增大以及肺泡管空气空间,而乙醇增强 ZD 加 DCA 饮食引起的肝损伤。这些发现表明,20 周的饮食性 ZD 加 DCA 处理会引起化学性食管损伤,但不会引起 Barrett 样病变。

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