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蜂胶和壳聚糖纳米颗粒对布洛芬诱导的白化大鼠肝毒性的保护作用。

Protective Effects of Propolis and Chitosan Nanoparticles against Ibuprofen-Induced Hepatotoxicity in Albino Rats.

作者信息

AlKandari Fajer M, Mohamed Hussein S, Ahmed Sayed A, Mahmoud Basant, Mahmoud Asmaa M

机构信息

Biochemistry Department, Faculty of Science, Beni-Suef University, Beni-Suef 62511, Egypt.

Chemistry Department of Medicinal and Aromatic Plants, Research Institute of Medicinal and Aromatic Plants (RIMAP), Beni-Suef University, Beni-Suef 62511, Egypt.

出版信息

Diseases. 2024 Feb 29;12(3):49. doi: 10.3390/diseases12030049.

Abstract

Post-marketing hepatotoxicity findings are more common or occur much later. NSAIDs (non-steroidal anti-inflammatory drugs) like ibuprofen are consumed in large quantities around the world. NSAIDs have a low incidence of hepatotoxicity but their wide use makes them a major contributor to drug-induced liver injury. Hepatitis is linked to systemic oxidative stress which results in cellular necrosis and fibrosis, as well as tissue lipoprotein peroxidation and glutathione depletion. Given the lack of safe and effective anti-hepatitis drugs in medicine today, natural substances appear to be a promising and safe alternative. Propolis and chitosan are considered natural substances that have a protective effect on the hepatocytes. The purpose of this study was to validate the protective effect of propolis/chitosan nanoparticle extracts on ibuprofen-induced hepatotoxicity. Thirty (30) albino rats were used for the experiment. Animals were exposed to ibuprofen (400 mg/kg body weight/day) for 4 weeks (7 days/week) followed by treatment with propolis (200 mg/kg body weight/day) and chitosan extract (200 mg/kg body weight/day) separately and also in combination for consecutive 4 weeks. This study revealed a significant increase in serum transaminases, alkaline phosphatase, albumin, and total bilirubin in serum, as well as an increase in lipid peroxidation (MDA) and nitric oxide (NO). Furthermore, GSH, GST, and SOD decreased significantly in the group that was exposed to ibuprofen. Furthermore, there was a significant increase in pro-inflammatory parameters such as IL-1β and NF-ĸB, as well as low levels of anti-inflammatory parameters such as IL-6 and BCl-2. These alterations were improved by propolis and chitosan extracts, which was further confirmed in experimental animals. This study demonstrated that propolis and chitosan nanoparticle extracts have the potential to protect against hepatotoxicity induced by ibuprofen, due to their ability to regulate anti-inflammatory and anti-oxidative defense activities.

摘要

上市后肝毒性发现更为常见或出现得更晚。布洛芬等非甾体抗炎药(NSAIDs)在全球范围内大量使用。NSAIDs肝毒性发生率较低,但由于其广泛使用,它们成为药物性肝损伤的主要原因。肝炎与全身氧化应激有关,氧化应激会导致细胞坏死和纤维化,以及组织脂蛋白过氧化和谷胱甘肽耗竭。鉴于当今医学中缺乏安全有效的抗肝炎药物,天然物质似乎是一种有前景且安全的替代品。蜂胶和壳聚糖被认为是对肝细胞有保护作用的天然物质。本研究的目的是验证蜂胶/壳聚糖纳米颗粒提取物对布洛芬诱导的肝毒性的保护作用。实验使用了30只白化大鼠。动物连续4周(每周7天)暴露于布洛芬(400毫克/千克体重/天),随后分别用蜂胶(200毫克/千克体重/天)和壳聚糖提取物(200毫克/千克体重/天)以及两者联合进行连续4周的治疗。本研究显示血清转氨酶、碱性磷酸酶、白蛋白和总胆红素显著升高,脂质过氧化(MDA)和一氧化氮(NO)增加。此外,暴露于布洛芬的组中谷胱甘肽(GSH)、谷胱甘肽S-转移酶(GST)和超氧化物歧化酶(SOD)显著降低。此外,促炎参数如白细胞介素-1β(IL-1β)和核因子-κB(NF-κB)显著增加,抗炎参数如白细胞介素-6(IL-6)和B细胞淋巴瘤-2(Bcl-2)水平较低。蜂胶和壳聚糖提取物改善了这些改变,这在实验动物中得到了进一步证实。本研究表明,蜂胶和壳聚糖纳米颗粒提取物有潜力预防布洛芬诱导的肝毒性,因为它们能够调节抗炎和抗氧化防御活性。

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