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A new cirrhotic animal protocol combining carbon tetrachloride with methotrexate to address limitations of the currently used chemical-induced models

四氯化碳 四氯化碳 肝硬化 甲氨蝶呤 氧化应激 医学 动物模型 药理学 免疫染色 病理 胃肠病学 内科学 化学 免疫组织化学 有机化学
作者
Rasha A. Mansouri,Adel M. Ahmad,Huda F. Alshaibi,Maha M. Al-Bazi,Abeer A. Banjabi,Hadeil M. Alsufiani,Akram Ahmed Aloqbi,Esam M. Aboubakr
出处
期刊:Frontiers in Pharmacology [Frontiers Media SA]
卷期号:14: 1201583-1201583 被引量:3
标识
DOI:10.3389/fphar.2023.1201583
摘要

Background: Chemically induced cirrhotic animal models are commonly used. However, they have limitations such as high mortalities and low yield of cirrhotic animals that limit their uses. Aims: To overcome limitations of the chemically induced cirrhotic animal model via combined administration of methotrexate (MTX) with CCl 4 and decrease their commonly used doses depending on the proposed synergetic cirrhotic effect. Methods: Rats were divided into six groups: normal (4 weeks), normal (8 weeks), MTX, CCl 4 (4 weeks), CCl 4 (8 weeks), and MTX + CCl 4 (4 weeks) groups. Animals’ hepatic morphology and histopathological characterization were explored. Hepatic Bcl2 and NF-κB-p65 tissue contents were determined using the immunostaining technique, and hepatic tissue damage, oxidative status, and inflammatory status biochemical parameters were determined. Results: CCl 4 + MTX combined administration produced prominent cirrhotic liver changes, further confirmed by a substantial increase in oxidative stress and inflammatory parameters, whereas mortalities were significantly lower than in other treated groups. Conclusion: The present study introduced a new model that can significantly improve the major limitations of chemically induced cirrhotic animal models with new pathological features that mimic human cirrhosis. Compared to other chemically induced methods, the present model can save time, cost, and animal suffering.
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