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首页> 外文期刊>Biological trace element research >Prophylactic role of a herbomineral drug 'Thamira parpam' against cysteamine-induced oxidative stress in liver and duodenum of rats.
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Prophylactic role of a herbomineral drug 'Thamira parpam' against cysteamine-induced oxidative stress in liver and duodenum of rats.

机译:人体矿物药物“ Thamira parpam”对半胱胺诱导的大鼠肝脏和十二指肠氧化应激的预防作用。

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摘要

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.
机译:铜在悉达多文献中被称为群马·卡兰(Gunma Kaalan),这意味着该药可有效治愈溃疡。根据Siddha的医学方法,用岩盐,酸橙汁,bra汁的生麦汁和,兰根汤煅烧纯化的铜箔,制得植物药“ Thamira parpam”。我们的研究调查了Thamira parpam(TP)在半胱胺诱发的十二指肠溃疡的治疗中的可能作用。向大鼠口服半胱胺(400 mg kg(-1)体重(-1),每4h间隔两次)导致高溃疡指数,TBARS升高,同时伴随着抗氧化剂的消耗,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(p <0.01)。用半胱胺攻击的中草药TP(0.5、1和2 mg / kg,p.o.)减弱了TBARS的升高和抗氧化剂的失衡。在肝炎性标志物的增加中,TP治疗中组织组织病理学改变并不严重。阳性对照奥美拉唑(25 mg / kg,体重,口服)在生化参数和组织组织学方面显示出明显的防止异常的保护作用。因此,我们的结果表明,在实验性诱导的大鼠肝脏和十二指肠损伤中,草本矿物药减轻氧化应激的作用可能是由自由基猝灭特性引起的。

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