Department of Biotechnology, University of Mysore, Manasagangotri, Mysore 570 006, India.
Food Chem Toxicol. 2013 Jul;57:179-84. doi: 10.1016/j.fct.2013.03.028. Epub 2013 Mar 29.
Hepatoprotective potential of the aqueous extract of the roots of Decalepis hamiltonii (DHA) against cyclophosphamide (CP)-induced oxidative stress has been investigated in mice. Administration of CP (25mg/kg b.w., i.p) for 10 days induced hepatic damage as indicated by the serum marker enzymes aspartate and alanine transaminases (AST, ALT), alkaline phosphatase (ALP) and lactate dehydrogenase (LDH). Parallel to these changes CP induced oxidative stress in the liver as evident from the increased lipid peroxidation (LPO), reactive oxygen species (ROS), depletion of glutathione (GSH), and reduced activities of the antioxidant enzymes such as superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR), and glutathione-S-transferase (GST). Treatment with DHA (50 and 100 mg/kg b.w., po) mitigated the CP-induced oxidative stress. Moreover, expression of genes for the antioxidant enzymes, were down-regulated by CP treatment which was reversed by DHA. Our study shows the DHA protected the liver from toxicity induced by CP and therefore, it could be serve as a safe medicinal supplement during cyclophosphamide chemotherapy.
已经在小鼠中研究了 Decalepis hamiltonii(DHA)根的水提取物对环磷酰胺(CP)诱导的氧化应激的肝保护作用。CP(25mg/kg b.w.,ip)连续 10 天给药导致血清标志物天冬氨酸和丙氨酸转氨酶(AST、ALT)、碱性磷酸酶(ALP)和乳酸脱氢酶(LDH)升高,表明肝损伤。与这些变化平行的是,CP 在肝脏中诱导了氧化应激,这表现在脂质过氧化(LPO)、活性氧(ROS)的增加、谷胱甘肽(GSH)的耗竭以及超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPx)、谷胱甘肽还原酶(GR)和谷胱甘肽-S-转移酶(GST)等抗氧化酶的活性降低。DHA(50 和 100mg/kg b.w.,po)治疗减轻了 CP 诱导的氧化应激。此外,CP 处理下调了抗氧化酶的基因表达,而 DHA 则逆转了这种下调。我们的研究表明,DHA 可防止 CP 引起的肝毒性,因此,它可作为环磷酰胺化疗期间的安全药物补充剂。