首页> 外文期刊>Indian Journal of Biochemistry & Biophysics >Protective effect of crude sulphated polysaccharide from Turbinaria ornata on isoniazid rifampicin induced hepatotoxicity and oxidative stress in the liver, kidney and brain of adult Swiss albino rats
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Protective effect of crude sulphated polysaccharide from Turbinaria ornata on isoniazid rifampicin induced hepatotoxicity and oxidative stress in the liver, kidney and brain of adult Swiss albino rats

机译:产于Turbinaria ornata的粗硫酸多糖对利福平异烟肼诱导的成年瑞士白化病大鼠肝,肾和脑的肝毒性和氧化应激的保护作用

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The bio activation of drugs to chemically active compounds, induces liver injury resulting in various degenerative diseases, which could be overcome by the administration of sulphated polysaccharides. The present study addresses, the hepatoprotective potential of crude sulphated polysaccharides (CSP) from emTurbinaria ornata/em using a Swiss albino rat model where liver damage was induced with Rifampicin (RMP) and Isoniazid (INH). The RMP-INH (75 mg/kg body weight) and CSP (10, 25, 50 and 200 mg/kg body weight) were orally administered to Swiss albino rat for 14 days. Silymarin (100 mg/kg body weight) administered group served as a positive control. At the end of the experiment serum was collected and the rats were dissected and the organs like liver, kidney and brain were collected. Administration of hepatotoxin causes increase in serum SGPT, SGOT, lipid peroxidation levels and a decrease in reduced glutathione, GST levels. Co-administration of CSP shows hepatoprotective activity on hepatotoxin induced damage. The hepatoprotective activity was also supported by histopathological studies of liver sections. In addition, our study revealed that the effect of toxicity induced in liver also caused damage to kidney and brain tissues resulting in decrease of total antioxidant status, reduced glutathione, increased levels of nitrate and macromolecular damage like lipid peroxidation. Co-administration of CSP significantly prevents the damage of liver, kidney and brain caused by hepatotoxin. The CSP (25 mg/kg body weight) from emT. ornata /em could be a better hepatoprotective agent than standard drug Silymarin." xml:lang="en_US.
机译:药物对化学活性化合物的生物激活会引起肝损伤,导致各种退行性疾病,可以通过施用硫酸化多糖来克服。本研究使用瑞士白化病大鼠模型研究了来自 Turbinaria ornata 的粗硫酸多糖(CSP)的肝保护潜力,该模型通过利福平(RMP)和异烟肼(INH)诱导肝损伤。将RMP-INH(75 mg / kg体重)和CSP(10、25、50和200 mg / kg体重)口服给予瑞士白化病大鼠14天。水飞蓟素(100 mg / kg体重)给药组作为阳性对照。实验结束时收集血清,解剖大鼠,收集肝,肾和脑等器官。服用肝毒素会导致血清SGPT,SGOT,脂质过氧化水平增加,而减少的谷胱甘肽,GST水平降低。 CSP的共同给药显示出对肝毒素诱导的损伤的肝保护活性。肝脏切片的组织病理学研究也支持了保肝活性。此外,我们的研究表明,在肝脏中诱导的毒性作用还导致肾脏和脑组织受损,从而导致总抗氧化剂状态降低,谷胱甘肽减少,硝酸盐水平升高以及大分子损害(如脂质过氧化反应)。 CSP的共同给药可有效预防肝毒素对肝脏,肾脏和大脑的损害。来自 T的CSP(25 mg / kg体重)。 Ornata 可能是比标准药物Silymarin更好的保肝剂。” xml:lang =“ zh_CN。”

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