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d-柠檬烯诱导大鼠肝损伤的组织病理学和生化评估

Histopathological and biochemical assessment of d-limonene-induced liver injury in rats.

作者信息

Ramos Carlos Alberto F, Sá Rita de Cássia da S, Alves Mateus F, Benedito Rubens B, de Sousa Damião P, Diniz Margareth de Fátima F M, Araújo Maria Salete T, de Almeida Reinaldo N

机构信息

Post-graduation Program in Bioactive Synthetic and Natural Products, Health Sciences Center, Federal University of Paraíba, Brazil.

Pharmaceutics Science Department, Health Sciences Center, Federal University of Paraíba, Brazil.

出版信息

Toxicol Rep. 2015 Jan 9;2:482-488. doi: 10.1016/j.toxrep.2015.01.001. eCollection 2015.

Abstract

The aim of the present work was to develop a biochemical, histologic and immunohistochemical study about the potential hepatotoxic effect of d-limonene - a component of volatile oils extracted from citrus plants. Blood alkaline phosphatase (ALP), aspartate aminotransferase (AST) and alanine aminotransferase (ALT) from d-limonene-treated animals were determined and compared to morphologic hepatic lesions in order to investigate the possible physiopathologic mechanisms involved in the liver toxicity, in experimental animals treated with d-limonene. Wistar rats were randomly divided into seven groups: two control groups (untreated or receiving only vehicle, tween-80); one positive control (vehicle); two experimental groups treated with d-limonene at doses of 25 mg/kg/day and 75 mg/kg/day for 45 days, and two other groups treated with the same doses for 30 days and kept under observation during 30 more days. Biochemical data showed significant reduction in ALT levels in the animals treated with 75 mg/kg of d-limonene. Histological analysis revealed some hepatocyte morphological lesions, including hydropic degeneration, microvesicular steatosis and necrosis, Kupffer cell hyperplasia and incipient fibrosis. By immunohistochemistry, influx of T (CD3+) and cytotoxic (CD8+) lymphocytes was observed in the rats treated with d-limonene at both dose levels. In conclusion, it is possible that d-limonene has been directly responsible for hepatic parenchymal and matrix damage following subchronic treatment with d-limonene.

摘要

本研究的目的是开展一项关于d-柠檬烯(一种从柑橘类植物中提取的挥发油成分)潜在肝毒性作用的生化、组织学和免疫组织化学研究。测定经d-柠檬烯处理动物的血液碱性磷酸酶(ALP)、天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT),并与肝脏形态学损伤进行比较,以研究在用d-柠檬烯处理的实验动物中,肝脏毒性可能涉及的生理病理机制。将Wistar大鼠随机分为七组:两个对照组(未处理或仅接受赋形剂吐温-80);一个阳性对照组(赋形剂);两个实验组,分别以25mg/kg/天和75mg/kg/天的剂量给予d-柠檬烯,持续45天,另外两组以相同剂量处理30天,并再观察30天。生化数据显示,用75mg/kg d-柠檬烯处理的动物中ALT水平显著降低。组织学分析显示一些肝细胞形态学损伤,包括水样变性、微泡性脂肪变性和坏死、库普弗细胞增生和早期纤维化。通过免疫组织化学观察到,在两个剂量水平下用d-柠檬烯处理的大鼠中均有T(CD3+)和细胞毒性(CD8+)淋巴细胞流入。总之,d-柠檬烯亚慢性处理后,肝脏实质和基质损伤可能直接由d-柠檬烯所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d85/5598502/2413bffb3b64/gr1.jpg

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