首页> 外文期刊>Metabolism: Clinical and Experimental >Oral adsorbent AST-120 ameliorates tubular injury in chronic renal failure patients by reducing proteinuria and oxidative stress generation.
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Oral adsorbent AST-120 ameliorates tubular injury in chronic renal failure patients by reducing proteinuria and oxidative stress generation.

机译:口服吸附剂AST-120通过减少蛋白尿和氧化应激的产生改善慢性肾衰竭患者的肾小管损伤。

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AST-120 is an oral adsorbent that attenuates the progression of chronic renal failure (CRF) and improves the prognosis of the patients under dialysis. Although tubulointerstitial injury is more important than glomerulopathy in terms of renal prognosis in patients with CRF, effect of AST-120 on tubular injury in CRF patients remains unknown. In this study, we examined whether and how AST-120 treatment could improve tubular damage in nondiabetic CRF patients. Fifty nondiabetic CRF patients were enrolled in the present study and divided into 2 groups: one was the AST-120-treated group (15 men and 10 women) and the other was the age-, sex-, and clinical variables-matched non-AST-120-treated control group. Patients were followed up for 12 months. We investigated the effects of AST-120 on serum levels of interleukin-6 (IL-6), proteinuria, and urinary excretion levels of 8-hydroxydeoxyguanosine (8-OHdG) and L-fatty acid binding protein (L-FABP), markers of oxidative stress and tubular injury, respectively. AST-120 treatment (6 g/d), but not control treatment, for 12 months significantly reduced IL-6, proteinuria, and urinary excretion levels of L-FABP and 8-OHdG, and inhibited the increase in serum creatinine in CRF patients. In univariate analyses, L-FABP levels were correlated with age, proteinuria, 8-OHdG, and IL-6. In multiple stepwise regression analysis, proteinuria and urinary 8-OHdG levels were independently related to L-FABP levels (R(2) = 0.605). Our present study demonstrated for the first time that AST-120 improved tubular injury in nondiabetic CRF patients. AST-120 may exert beneficial effects in CRF patients by protecting tubular damage partly via reduction of proteinuria and oxidative stress generation.
机译:AST-120是一种口服吸附剂,可减轻慢性肾功能衰竭(CRF)的进程并改善透析患者的预后。尽管就肾衰竭而言,肾小管间质损伤比肾小球病变更为重要,但AST-120对肾衰竭患者肾小管损伤的影响仍未知。在这项研究中,我们检查了AST-120治疗是否以及如何改善非糖尿病CRF患者的肾小管损伤。本研究招募了50名非糖尿病CRF患者,分为2组:一组是AST-120治疗组(15名男性和10名女性),另一组是年龄,性别和临床变量匹配的非糖尿病患者。 AST-120治疗的对照组。对患者进行了12个月的随访。我们调查了AST-120对血清白细胞介素6(IL-6),蛋白尿以及尿液中8-羟基脱氧鸟嘌呤(8-OHdG)和L-脂肪酸结合蛋白(L-FABP)排泄水平的影响。氧化应激和肾小管损伤。 AST-120治疗(6 g / d),而非对照治疗,持续12个月可显着降低CRF患者的IL-6,蛋白尿和尿排泄L-FABP和8-OHdG水平,并抑制血清肌酐的升高。在单变量分析中,L-FABP水平与年龄,蛋白尿,8-OHdG和IL-6相关。在多个逐步回归分析中,蛋白尿和尿中的8-OHdG水平与L-FABP水平独立相关(R(2)= 0.605)。我们目前的研究首次证明AST-120可改善非糖尿病CRF患者的肾小管损伤。 AST-120可通过部分减少蛋白尿和氧化应激的产生来保护肾小管损伤,从而在CRF患者中发挥有益作用。

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