Sharma Veena, Paliwal Ritu, Janmeda Pracheta, Sharma Shatruhan
Department of Bioscience and Biotechnology, Banasthali University, Banasthali, India.
Asian Pac J Cancer Prev. 2012;13(6):2563-9. doi: 10.7314/apjcp.2012.13.6.2563.
Oxidative stress is a common mechanism contributing to initiation and progression of hepatic damage in a variety of liver disorders. Hence there is a great demand for the development of agents with potent antioxidant effect. The aim of the present investigation is to evaluate the efficacy of Moringa oleifera as a hepatoprotective and an antioxidant against 7, 12-dimethylbenz[a]anthracene induced hepatocellular damage. Single oral administration of DMBA (15 mg/kg) to mice resulted in significantly (p<0.001) depleted levels of xenobiotic enzymes like, cytochrome P450 and b5. DMBA induced oxidative stress was confirmed by decreased levels of reduced glutathione (GSH) and glutathione-S-transferase (GST) in the liver tissue. The status of hepatic aspartate transaminase (AST), alanine transaminase (ALT), and alkaline phosphatase (ALP) which is indicative of hepatocellular damage were also found to be decreased in DMBA administered mice. Pretreatment with the Moringa oleifera (200 and 400 mg/kg) orally for 14 days significantly reversed the DMBA induced alterations in the liver tissue and offered almost complete protection. The results from the present study indicate that Moringa oleifera exhibits good hepatoprotective and antioxidant potential against DMBA induced hepatocellular damage in mice that might be due to decreased free radical generation.
氧化应激是导致多种肝脏疾病肝损伤发生和发展的常见机制。因此,对具有强大抗氧化作用的药物的开发有很大需求。本研究的目的是评估辣木对7,12-二甲基苯并[a]蒽诱导的肝细胞损伤的保肝和抗氧化功效。给小鼠单次口服DMBA(15毫克/千克)导致异生素酶如细胞色素P450和b5的水平显著(p<0.001)降低。肝脏组织中还原型谷胱甘肽(GSH)和谷胱甘肽-S-转移酶(GST)水平降低证实了DMBA诱导的氧化应激。在给予DMBA的小鼠中还发现,指示肝细胞损伤的肝天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)和碱性磷酸酶(ALP)的状态也降低。口服辣木(200和400毫克/千克)预处理14天可显著逆转DMBA诱导的肝脏组织改变,并提供几乎完全的保护。本研究结果表明,辣木对DMBA诱导的小鼠肝细胞损伤具有良好的保肝和抗氧化潜力,这可能是由于自由基生成减少所致。