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顺铂、阿霉素和5-氟尿嘧啶(5-FU)对雄性白化大鼠肝脏的组织病理学影响。

Histopathological effects of cisplatin, doxorubicin and 5-flurouracil (5-FU) on the liver of male albino rats.

作者信息

El-Sayyad Hassan I, Ismail Mohamed F, Shalaby F M, Abou-El-Magd R F, Gaur Rajiv L, Fernando Augusta, Raj Madhwa H G, Ouhtit Allal

机构信息

Department of Zoology, Faculty of Science, Mansoura University, Egypt.

出版信息

Int J Biol Sci. 2009 Jun 28;5(5):466-73. doi: 10.7150/ijbs.5.466.

Abstract

Cisplatin, doxorubicin and fluorouracil (5-FU), drugs belonging to different chemical classes, have been extensively used for chemotherapy of various cancers. Despite extensive investigations into their hepatotoxicity, there is very limited information on their effects on the structure and ultra-structure of liver cells in vivo. Here, we demonstrate for the first time, the effects of these three anticancer drugs on rat liver toxicity using both light and electron microscopy. Light microscopic observations revealed that higher doses of cisplatin and doxorubicin caused massive hepatotoxicity compared to 5-FU treatment, including dissolution of hepatic cords, focal inflammation and necrotic tissues. Interestingly, low doses also exhibited abnormal changes, including periportal fibrosis, degeneration of hepatic cords and increased apoptosis. These changes were confirmed at ultrastructural level, including vesiculated rough endoplasmic reticulum and atrophied mitochondria with ill-differentiated cisternae, dense collection of macrophages and lymphocytes as well as fibrocytes with collagenous fibrils manifesting early sign of fibrosis, especially in response to cisplatin and doxorubicin -treatment. Our results provide in vivo evidence, at ultrastructural level, of direct hepatotoxicity caused by cisplatin, doxorubicin and 5-FU at both light and electron microscopi. These results can guide the design of appropriate treatment regimen to reduce the hepatotoxic effects of these anticancer drugs.

摘要

顺铂、阿霉素和氟尿嘧啶(5-FU)属于不同化学类别,已被广泛用于各种癌症的化疗。尽管对它们的肝毒性进行了广泛研究,但关于它们在体内对肝细胞结构和超微结构影响的信息非常有限。在此,我们首次使用光学显微镜和电子显微镜证明了这三种抗癌药物对大鼠肝脏毒性的影响。光学显微镜观察显示,与5-FU治疗相比,更高剂量的顺铂和阿霉素会导致大量肝毒性,包括肝索溶解、局灶性炎症和坏死组织。有趣的是,低剂量也表现出异常变化,包括门静脉周围纤维化、肝索变性和凋亡增加。这些变化在超微结构水平得到证实,包括泡状粗面内质网和萎缩的线粒体,其池分化不良,巨噬细胞和淋巴细胞密集聚集,以及具有胶原纤维的成纤维细胞表现出纤维化的早期迹象,尤其是在顺铂和阿霉素治疗后。我们的结果在超微结构水平上提供了体内证据,证明顺铂、阿霉素和5-FU在光学显微镜和电子显微镜下均具有直接肝毒性。这些结果可以指导设计适当的治疗方案,以降低这些抗癌药物的肝毒性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e17/2706427/df6eb4ccf5c7/ijbsv05p0466g01.jpg

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