黄魔芋对硫乙酰胺致大鼠肝硬化的急性毒性及肝保护作用。

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Acta Pharmaceutica Pub Date : 2025-04-10 Print Date: 2025-03-01 DOI:10.2478/acph-2025-0007
Riyadh Zainadin Mawlood, Kamaran Abdoulrahman
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引用次数: 0

摘要

黄斑魔芋是一种药用植物,在传统医学中用于治疗肝脏疾病。本研究的目的是评估黄芪叶乙醇提取物对硫代乙酰胺(TAA)诱导的Sprague- Dawley大鼠肝硬化的肝保护作用。大鼠每周腹腔注射3次硫乙酰胺(TAA)治疗2个月。组织病理学检查显示,硫乙酰胺对照组肝损伤较水飞蓟素组严重(p < 0.05)。此外,a .欧治疗导致了促炎细胞因子肿瘤坏死因子-α和il - 6,正常化和增加抗炎细胞因子il - 10的表达(p < 0.05)。由此可见,黄斑藤叶对TAA所致大鼠肝硬化可能具有保护肝脏的作用,并具有抗氧化和抗炎作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute toxicity and hepatoprotective effect of Arum maculatum on rat liver cirrhosis induced with thioacetamide.

Arum maculatum is a medicinal plant that has been employed in traditional medicine for treating liver diseases. The objective of the current study was to evaluate the hepatoprotective impacts of ethanolic extract of the A. maculatum leaves on cirrhosis induced by thioacetamide (TAA) in Sprague--Dawley rats. The rats were treated for two months with thioacetamide (TAA) administered intraperitoneally thrice weekly. Histopathological examination revealed severe liver damage in the thioacetamide control group, while the silymarin treatments (p < 0.05). Furthermore, A. maculatum treatment led to the normalization of pro-inflammatory cytokines TNF-α and IL-6, and increased expression of the anti-inflammatory cytokine IL-10 (p < 0.05). Thus, A. maculatum leaves might have a hepatoprotective role in rat liver cirrhosis induced by TAA, along with antioxidant and anti-inflammatory effects.

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来源期刊
Acta Pharmaceutica
Acta Pharmaceutica PHARMACOLOGY & PHARMACY-
CiteScore
5.20
自引率
3.60%
发文量
20
审稿时长
>12 weeks
期刊介绍: AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.
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