肉桂、肉桂醛和山奈酚对对乙酰氨基酚致小鼠急性肝损伤和细胞凋亡的保护作用

Zulfia Hussain
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引用次数: 8

摘要

肝病是巴基斯坦的主要健康问题之一。本研究探讨肉桂、肉桂醛和山奈酚对对乙酰氨基酚(APAP)所致肝损伤的保护作用机制。对肉桂醇提物进行了定性植物化学分析。为了进行体内评价,Balb/c小鼠分别给予肉桂提取物(200 mg/kg ig)、肉桂醛(10 mg/kg ig)和山奈酚(10 mg/kg ig) 14天,然后给予APAP (200 mg/kg ig)。试验结束时解剖小鼠,取血、肝、脾标本进行生化、组织病理学及凋亡基因表达分析。对结果的显著性进行统计学分析。结果表明,APAP给药8 h小鼠肝损伤明显,且损伤程度加重。肉桂提取物、肉桂醛和山奈酚预处理可通过降低血清总蛋白和胆红素升高来改善APAP所致的器官损伤。此外,APAP通过上调Bad、Bax和Caspase-3,下调Bcl-2,严重改变肝脏组织学,但不影响脾脏组织学。然而,肉桂、肉桂醛和山奈酚预处理可能通过其抗氧化活性改善了apap诱导的肝脏改变和细胞凋亡。此外,与单独使用肉桂提取物相比,肉桂醛和山奈酚在低剂量下具有相当的保护潜力,提示低剂量对apap诱导的肝损伤和细胞凋亡具有治疗潜力。
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Protective Effects of Cinnamon, Cinnamaldehyde and Kaempferol against Acetaminophen-Induced Acute Liver Injury and Apoptosis in Mouse Model
Liver diseases are among the major health problems in Pakistan. The present study investigated the mechanism of hepatoprotection by cinnamon, cinnamaldehyde and kaempferol in Acetaminophen (APAP)-induced liver injury. Qualitative phytochemical analysis was performed for standardization of cinnamon ethanolic extract. For in-vivo evaluation, Balb/c mice were administered with cinnamon extract (200 mg/kg i.g.), cinnamaldehyde (10 mg/kg i.g.) and kaempferol (10 mg/kg i.g.) for 14 days followed by administration of APAP (200 mg/kg i.p.). At the end of trial, mice were dissected, and blood, liver and spleen samples were collected for biochemical, histopathological and apoptotic genes expression analysis. Statistical analysis was performed for significance of results. The results showed that the hepatic damage due to APAP administration for 8 hours in mice was apparent with increased severity. Cinnamon extract, cinnamaldehyde and kaempferol pretreatment suggested ameliorative effects on organ injury induced by APAP by decreasing the elevated serum levels of total proteins and bilirubin. In addition, APAP exerted severe alterations on liver histology without affecting spleen histology alongwith upregulation of Bad, Bax and Caspase-3 and downregulation of Bcl-2. However, cinnamon, cinnamaldehyde and kaempferol pretreatment ameliorated APAPinduced liver alterations and apoptosis, possibly through their antioxidant activity. In addition, cinnamaldehyde and kaempferol possessed comparable protective potential at 20-times less dose as compared to cinnamon extract alone, suggesting therapeutic potential at lower dose in APAP-induced liver injury and apoptosis.
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