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四氯化碳对仓鼠气管上皮细胞的影响。

Effect of carbon tetrachloride on hamster tracheal epithelial cells.

作者信息

Ahmadizadeh M, Echt R, Heusner W W, Ross L M, Roth R A

机构信息

Department of Anatomy, Michigan State University, East Lansing 48824.

出版信息

J Toxicol Environ Health. 1990 Aug;30(4):273-85. doi: 10.1080/15287399009531429.

Abstract

This study was designed to assess effects of carbon tetrachloride (CCl4) in hamster tracheal epithelium. Adult, male, Syrian golden hamsters were treated with 2.5 ml/kg CCl4 ip, and controls received only the vehicle (peanut oil). Animals were sacrificed after 1, 4, 12, and 24 h. Tissue samples from upper and lower tracheal levels were fixed and embedded in glycol methacrylate for light microscopy. Some tracheal rings were also fixed in formaldehyde/glutaraldehyde cacodylate buffer for transmission electron microscopy. For histopathologic evaluation of the tracheal epithelial cells, each tracheal level was cut transversely at 3 microns and stained with toluidine blue. CCl4 produced injury to ciliated and nonciliated cells in all portions of hamster trachea, although the severity of CCl4-induced injury differed in various levels and regions. The number of damaged cells increased markedly after 1 h in the lower trachea, but not until after 4 h in the upper trachea. By 24 h, the number of injured cells had decreased so that no significant difference from control was evident. The ultrastructural alterations in epithelial cells were obvious as early as 1 h after CCl4 administration. Intracellular organelles, including smooth and rough endoplasmic reticulum, mitochondria, and Golgi apparatuses, were damaged by this chemical. Since CCl4-induced cell injury is dependent on metabolism by intracellular NADPH-dependent cytochrome P450 monooxygenases, these results suggest that hamster tracheal epithelial cells have the potential to activate CCl4 metabolically.

摘要

本研究旨在评估四氯化碳(CCl4)对仓鼠气管上皮的影响。成年雄性叙利亚金黄仓鼠经腹腔注射2.5 ml/kg CCl4,对照组仅给予溶媒(花生油)。在1、4、12和24小时后处死动物。取自气管上下段的组织样本固定后包埋于甲基丙烯酸乙二醇酯中用于光学显微镜检查。一些气管环也固定于甲醛/戊二醛二甲胂酸盐缓冲液中用于透射电子显微镜检查。为了对气管上皮细胞进行组织病理学评估,将每个气管段横向切成3微米厚,并用甲苯胺蓝染色。CCl4对仓鼠气管各部位的纤毛细胞和非纤毛细胞均造成损伤,尽管CCl4诱导的损伤严重程度在不同水平和区域有所不同。下呼吸道在1小时后受损细胞数量显著增加,而上呼吸道直到4小时后才出现这种情况。到24小时时,受损细胞数量减少,与对照组无明显差异。早在给予CCl4后1小时,上皮细胞的超微结构改变就很明显。包括滑面和粗面内质网、线粒体和高尔基体在内的细胞内细胞器均被这种化学物质损伤。由于CCl4诱导的细胞损伤依赖于细胞内依赖烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的细胞色素P450单加氧酶的代谢,这些结果表明仓鼠气管上皮细胞具有代谢激活CCl4的潜力。

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