Suppr超能文献

镉诱导大鼠肝脏超微结构变化的时间进程。

Time course of cadmium-induced ultrastructural changes in rat liver.

作者信息

Dudley R E, Svoboda D J, Klaassen C D

出版信息

Toxicol Appl Pharmacol. 1984 Oct;76(1):150-60. doi: 10.1016/0041-008x(84)90038-3.

Abstract

Ultrastructural changes in rat liver were studied 1, 2, 4, 6, 8, and 10 hr after administration of a single, high dose of Cd (3.9 mg Cd/kg, iv) or after repeated administration of a lower dose (0.5 mg Cd/kg, sc, 6 days/week for 6 months). These dosing regimens have been previously shown to produce hepatotoxicity and result in large accumulations of Cd in liver. In addition to light and electron microscopy, plasma enzyme activities indicative of liver injury, namely alanine (ALT) and aspartate (AST) aminotransferase, were determined at the aforementioned times. One hour after an acute dose of Cd, electron photomicrographs of liver showed dilation of the rough endoplasmic reticulum with concomitant loss of membrane-associated ribosomes, nucleolar condensation, and an increase in the number of perichromatin granules. At later times (4 and 6 hr), ultrastructural changes included mitochondrial swelling associated with matrical inclusions, further dilation and vesiculation of rough endoplasmic reticulum, and presence of a fibrillar material within cytoplasm. In contrast to changes observed after single administration of Cd, the predominant hepatic lesions in rats injected repeatedly with the metal over 6 months were interstitial fibrosis, nuclear enlargement, and an increase in number and predominance of nucleoli. Ultrastructural evidence of nuclear alterations included condensation of nucleoli and an increase in the number of perichromatin granules. These results indicate that Cd interferes with hepatic protein synthesis early after injection of a large dose, and that further degenerative changes occur later and possibly in response to protein inhibition. Although severe degenerative changes in liver were not evident in rats chronically exposed to the metal, Cd-induced changes in nuclei and nucleoli also indicate the likelihood of altered protein synthesis.

摘要

在单次静脉注射高剂量镉(3.9毫克镉/千克)或反复皮下注射低剂量镉(0.5毫克镉/千克,每周6天,共6个月)后的1、2、4、6、8和10小时,对大鼠肝脏的超微结构变化进行了研究。这些给药方案先前已被证明会产生肝毒性,并导致肝脏中大量镉蓄积。除了光学显微镜和电子显微镜检查外,还在上述时间测定了指示肝损伤的血浆酶活性,即丙氨酸(ALT)和天冬氨酸(AST)转氨酶。急性剂量的镉注射后1小时,肝脏的电子显微照片显示粗面内质网扩张,同时膜结合核糖体丢失、核仁凝聚,以及染色质周围颗粒数量增加。在随后的时间(4和6小时),超微结构变化包括线粒体肿胀并伴有基质内含物、粗面内质网进一步扩张和形成囊泡,以及细胞质内出现纤维状物质。与单次注射镉后观察到的变化相反,在6个月内反复注射该金属的大鼠中,主要的肝脏病变是间质纤维化、核肿大,以及核仁数量增加和占优势。核改变的超微结构证据包括核仁凝聚和染色质周围颗粒数量增加。这些结果表明,大剂量注射镉后早期镉会干扰肝脏蛋白质合成,并且随后会发生进一步的退行性变化,可能是对蛋白质抑制的反应。尽管长期接触该金属的大鼠肝脏中没有明显的严重退行性变化,但镉诱导的细胞核和核仁变化也表明蛋白质合成改变的可能性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验