Suppr超能文献

新型实验性抗肿瘤药物二氮杂芴衍生物AC - 3579(NSC - 170561)对大鼠肝癌的影响。

Effects of the diazafluoranthen derivative AC-3579 (NSC-170561), a new experimental antitumour drug, on rat hepatoma.

作者信息

Thys O, Hildebrand J, Gerin Y

出版信息

Pathol Eur. 1975;10(4):251-62.

PMID:174050
Abstract

The effects of AC-3579 (NSC-170561), a new experimental antitumour drug which depresses phospholipid catabolism in liver, were compared in rat aflatoxin-induced hepatoma and in non-neoplastic hepatocytes surrounding the tumour. Ultrastructural lesions, characterized by the hypertrophy of the smooth endoplasmic reticulum and the presence of lamellate cytosomes appeared in both tissues. They were less marked in hepatoma than in non-neoplastic cells. As in control livers, they were related to an invrease in pohspholipid concentration due to the decrease of phospholipid breakdown. In addition, chemical analysis demonstrated differences between hepatoma, non-neoplastic aflatoxin-treated liver and control liver: total and free cholesterol were decreased, relative concentration of sphingomyelin increased and that of phosphatidylethanolamine decreased by about 50%, in both hepatoma and non-neoplastic liver. Phospholipid concentration was decreased by 50% in tumour cells. After AC-3579 treatment total cholesterol was increased 3.2 fold in non-neoplastic liver and 2.5 fold in hepatoma but not in control liver.

摘要

新型实验性抗肿瘤药物AC-3579(NSC-170561)可抑制肝脏中的磷脂分解代谢,我们比较了其在大鼠黄曲霉毒素诱导的肝癌组织以及肿瘤周围非肿瘤性肝细胞中的作用。超微结构损伤表现为滑面内质网肥大和出现层状胞质小体,这两种组织中均有此现象。肝癌组织中的这些损伤不如非肿瘤性细胞中明显。与对照肝脏一样,这些损伤与磷脂分解减少导致的磷脂浓度增加有关。此外,化学分析表明,肝癌组织、经黄曲霉毒素处理的非肿瘤性肝脏和对照肝脏之间存在差异:肝癌组织和非肿瘤性肝脏中的总胆固醇和游离胆固醇均降低,鞘磷脂的相对浓度增加,磷脂酰乙醇胺的相对浓度降低约50%。肿瘤细胞中的磷脂浓度降低了50%。AC-3579处理后,非肿瘤性肝脏中的总胆固醇增加了3.2倍,肝癌组织中增加了2.5倍,而对照肝脏中未增加。

相似文献

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