利用对乙酰氨基酚诱导的氧化应激小鼠模型,比较表征肉桂、肉桂醛和山奈酚的植物化学、抗氧化和药理特性

Zulfia Hussain, Junaid Ali Khan, M. Arshad, F. Muhammad, R. Z. Abbas
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引用次数: 3

摘要

本研究旨在探讨肉桂皮提取物、肉桂醛和山奈酚对乙酰氨基酚(APAP)诱导的氧化应激的比较疗效。用肉桂皮提取物、肉桂醛和山奈酚进行体内分析。从体外筛选试验的结果中,选择肉桂醇提取物进行小鼠模型的体内研究。为此,Balb/c白化小鼠分别口服肉桂乙醇提取物(200 mg/kg)、肉桂醛(10 mg/kg)和山奈酚(10 mg/kg) 14天,然后8小时内单次腹腔注射APAP。采集血液和器官标本进行生化和组织病理学分析。结果表明,肉桂皮乙醇提取物、肉桂醛和山奈酚可改善apap诱导的小鼠氧化应激和器官毒性。总之,肉桂醛和山奈酚具有相当的抗氧化潜力,即使剂量比肉桂树皮乙醇提取物少20倍,这表明肉桂醛和山奈酚在氧化应激相关疾病中具有治疗潜力。
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Comparative characterization of cinnamon, cinnamaldehyde and kaempferol for phytochemical, antioxidant and pharmacological properties using acetaminophen-induced oxidative stress mouse model
This study was aimed to explore the comparative efficacy of cinnamon bark extract, cinnamaldehyde and kaempferol against acetaminophen (APAP)-induced oxidative stress. Cinnamon bark extract, cinnamaldehyde and kaempferol were utilized for in-vivo analysis. From the results of in-vitro screening tests, cinnamon ethanolic extract was selected for in-vivo study in mouse model. For this, Balb/c albino mice were treated with cinnamon ethanolic extract (200 mg/kg), cinnamaldehyde (10 mg/kg) and kaempferol (10 mg/kg) orally for 14 days followed by single intraperitoneal administration of APAP during 8 hours. Blood and organ samples were collected for biochemical and histopathological analysis. The results showed that cinnamon bark ethanolic extract, cinnamaldehyde and kaempferol ameliorated APAP-induced oxidative stress and organ toxicity in mice. In conclusion, cinnamaldehyde and kaempferol possess comparable antioxidant potential even at 20-times less dose as compared to cinnamon bark ethanolic extract suggesting therapeutic potential in oxidative stress-related disorders.
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