Sacran, a High-molecular Weight Polysaccharide Inhibits Renal Injury and Oxidative Stress in Chronic Renal Failure Model Rats

Miwa Goto, D. Iohara, Shinichiro Kaneko, T. Higashi, K. Motoyama, H. Arima, T. Maruyama, K. Uekama, F. Hirayama, M. Anraku, M. Otagiri
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引用次数: 1

Abstract

The administration of a high-molecular polysaccharide Sacran results in a significant decrease in renal injury and oxidative stress, compared with that for the oral carbonaceous adsorbent, AST-120 (Kremezin®) or a non-treatment group in 5/6 nephrectomized rats. An oral administration of Sacran (20 mg/day) over a 4 week period resulted in a significant decrease in serum indoxyl sulfate, creatinine and urea nitrogen levels, compared with a similar treatment with AST-120 or the non-treatment group. Sacran treatment also resulted in antioxidant potential being maintained, compared with that for AST-120 or the non-treatment group. Immuno-histochemical analyses also demonstrated that CRF rats, when treated with Sacran, showed a decrease in the level of accumulated renal fibrosis and 8-OHdG compared with AST-120 or the non-treatment group. These results suggest that the ingestion of Sacran results in a significant reduction in the levels of prooxidants, such as uremic toxins, in the gastrointestinal tract, thereby inhibiting the subsequent development of oxidative stress in the systemic circulation.
高分子量多糖多糖多糖对慢性肾衰竭模型大鼠肾损伤和氧化应激的抑制作用
与口服碳质吸附剂、AST-120 (Kremezin®)或未给药组相比,给药高分子多糖Sacran可显著降低5/6肾切除大鼠的肾损伤和氧化应激。与AST-120或非治疗组相比,口服沙克兰(20mg /天)4周后,血清硫酸吲哚酚、肌酐和尿素氮水平显著降低。与AST-120组或未治疗组相比,Sacran治疗也使抗氧化潜能得以维持。免疫组织化学分析还表明,与AST-120或未治疗组相比,经Sacran治疗的CRF大鼠的肾纤维化和8-OHdG水平均有所下降。这些结果表明,摄入沙克兰可显著降低胃肠道中促氧化剂(如尿毒症毒素)的水平,从而抑制随后在体循环中氧化应激的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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