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大鼠在单独或联合3天间歇性暴露于甲醛和臭氧后鼻上皮的生化和组织病理学变化。

Biochemical and histopathological changes in nasal epithelium of rats after 3-day intermittent exposure to formaldehyde and ozone alone or in combination.

作者信息

Cassee F R, Feron V J

机构信息

Department of Biological Toxicology, TNO Toxicology and Nutrition Institute, AJ Zeist, The Netherlands.

出版信息

Toxicol Lett. 1994 Jun;72(1-3):257-68. doi: 10.1016/0378-4274(94)90037-x.

Abstract

To get a better insight into the pathophysiology of the nasal changes induced by formaldehyde-ozone mixtures, a 3-day inhalation study was carried out in rats, using intermittent exposure to formaldehyde (3.6 ppm) and ozone (0.4 ppm) alone or in combination and focusing on biochemical and histopathological changes in rat nasal respiratory epithelium. Formaldehyde dehydrogenase, glutathione S-transferase, glutathione reductase, and glucose-6-phosphate dehydrogenase activities in this epithelium were not affected by the individual compounds. However, combined exposure to formaldehyde and ozone resulted in slightly decreased activities of these enzymes. Formaldehyde was found to induce rhinitis, degeneration, frank necrosis, hyperplasia and squamous metaplasia of the ciliated and non-ciliated nasal respiratory epithelium, while ozone induced disarrangement, flattening and slight basal cell hyperplasia of the non-ciliated cuboidal epithelium accompanied by influx of neutrophils. Proliferating cell nuclear antigen (PCNA) expression was elevated not only in nasal areas showing ozone-induced histopathological changes but also in the otherwise normal-appearing epithelium of the nasal septum. No interactive effects were found with respect to proliferative response of the nasal respiratory epithelium after exposure to the formaldehyde-ozone mixture. The present study did not provide evidence of a major role of glutathione and glutathione-dependent enzymes in the pathogenesis of nasal lesions induced by formaldehyde and/or ozone, demonstrated the potential of ozone to affect the mucociliary epithelium lining the nasal septum, and suggested that PCNA expression is a sensitive tool for detection of early effects of respiratory irritants.

摘要

为了更深入了解甲醛 - 臭氧混合物引起的鼻腔变化的病理生理学,对大鼠进行了一项为期3天的吸入研究,采用单独或联合间歇性暴露于甲醛(3.6 ppm)和臭氧(0.4 ppm),并重点关注大鼠鼻呼吸上皮的生化和组织病理学变化。该上皮中的甲醛脱氢酶、谷胱甘肽S - 转移酶、谷胱甘肽还原酶和葡萄糖 - 6 - 磷酸脱氢酶活性不受单一化合物的影响。然而,甲醛和臭氧联合暴露导致这些酶的活性略有下降。发现甲醛可诱导鼻呼吸上皮的鼻炎、变性、明显坏死、增生和鳞状化生,而臭氧可诱导非纤毛立方上皮的排列紊乱、扁平及轻微基底细胞增生,并伴有中性粒细胞浸润。增殖细胞核抗原(PCNA)表达不仅在显示臭氧诱导的组织病理学变化的鼻腔区域升高,而且在鼻中隔外观正常的上皮中也升高。暴露于甲醛 - 臭氧混合物后,鼻呼吸上皮的增殖反应未发现交互作用。本研究没有提供证据表明谷胱甘肽和谷胱甘肽依赖性酶在甲醛和/或臭氧诱导的鼻腔病变发病机制中起主要作用,证明了臭氧影响鼻中隔黏膜纤毛上皮的可能性,并表明PCNA表达是检测呼吸道刺激物早期效应的敏感工具。

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