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草药矿物药物“Thamira parpam”对半胱胺诱导的大鼠肝和十二指肠氧化应激的预防作用。

Prophylactic role of a herbomineral drug "Thamira parpam" against cysteamine-induced oxidative stress in liver and duodenum of rats.

机构信息

Herbal and Indian Medicine Research Laboratory, Department of Biochemistry, Sri Ramachandra University, Porur, Chennai 600116, India.

出版信息

Biol Trace Elem Res. 2010 Dec;138(1-3):212-25. doi: 10.1007/s12011-009-8602-8. Epub 2010 Feb 18.

Abstract

Copper is known as Gunma Kaalan in Siddha literature, which means that the drug is effective for healing ulcers. The herbomineral drug "Thamira parpam" is prepared by calcining the purified copper foils with rock salt, lime juice, bracteated birth wort juice, and Alangium root decoction according to Siddha medicine. Our study investigated the possible role of Thamira parpam (TP) in the management of cysteamine-induced duodenal ulcers. Cysteamine (400 mg kg(-1) body weight(-1), two doses at 4 h interval) orally given to rats resulted in high ulcer index, increased TBARS with concomitant depletion of antioxidants such as superoxide dismutase, glutathione, glutathione peroxidase, and inflammatory markers cathepsin D, and myeloperoxidase (p < 0.01). Herbomineral drug TP (0.5, 1, and 2 mg/kg, p.o.) challenged with cysteamine attenuated the elevation of TBARS and imbalance of antioxidants. In the increases in liver inflammatory markers, tissue histopathology changes were not severe in TP treatment. Positive control omeprazole (25 mg/kg, body weight, orally) showed considerable protection against anomaly in biochemical parameters and tissue histology. Hence, our results indicate that the attenuation of oxidative stress by the herbomineral drug in experimentally induced damage to liver and duodenum of rats could be mediated by free radical quenching property.

摘要

铜在顺势疗法文献中被称为古马卡兰,这意味着这种药物对治疗溃疡有效。草药矿物药物“塔米拉帕尔帕姆”是根据顺势疗法制备的,方法是用岩盐、石灰汁、有苞片的益母草汁和冬葵根汤煅烧纯化的铜箔。我们的研究调查了塔米拉帕尔帕姆(TP)在半胱胺诱导的十二指肠溃疡治疗中的可能作用。半胱胺(400mgkg(-1)体重(-1),4 小时间隔口服两次)给药大鼠导致溃疡指数升高,TBARS 增加,同时抗氧化剂如超氧化物歧化酶、谷胱甘肽、谷胱甘肽过氧化物酶和炎症标志物组织蛋白酶 D 和髓过氧化物酶耗竭(p<0.01)。用半胱胺挑战的草药矿物药物 TP(0.5、1 和 2mg/kg,po)减轻了 TBARS 的升高和抗氧化剂的失衡。在肝炎症标志物的增加中,TP 治疗的组织组织病理学变化不严重。阳性对照奥美拉唑(25mgkg(-1)体重,口服)对生化参数和组织组织学异常表现出相当大的保护作用。因此,我们的结果表明,草药矿物药物对大鼠肝和十二指肠实验性损伤的氧化应激的抑制作用可能是通过自由基猝灭特性介导的。

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