首页> 外文期刊>Nephron >Spherical Carbon Adsorbent (AST-120) Protects Deterioration of Renal Function in Chronic Kidney Disease Rats through Inhibition of Reactive Oxygen Species Production from Mitochondria and Reduction of Serum Lipid Peroxidation
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Spherical Carbon Adsorbent (AST-120) Protects Deterioration of Renal Function in Chronic Kidney Disease Rats through Inhibition of Reactive Oxygen Species Production from Mitochondria and Reduction of Serum Lipid Peroxidation

机译:球形碳吸附剂(AST-120)通过抑制线粒体产生的活性氧并减少血清脂质过氧化作用来保护慢性肾脏病大鼠的肾功能恶化

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Background/Aim: An imbalance in renal redox status contributes to progression of renal dysfunction. We investigated the effects of an oral charcoal adsorbent (AST-120) on renal redox status, superoxide production from renal mitochondria, and serum lipid peroxidation using chronic kidney disease (CKD) model rats. Methods: CKD was induced by 5/6 nephrectomy. CKD rats were divided into 2 groups: controls, and those treated with AST-120 for 20 weeks. We evaluated: (1) renal redox status by in vivo low-frequency electron spin resonance imaging (EPRI); (2) renal superoxide scavenging activity (SSA); (3) superoxide production from renal mitochondria; (4) immunostaining for Cu-Zn superoxide dis-mutase (SOD), and (5) oxidative stress markers including LDL-negative charge (LDL-CMF), serum lipid peroxide (LPO) and urinary hexanoyl-lysine (HEL). The effect of indoxyl sulfate, a uremic toxin, on mitochondrial superoxide production was also investigated. Results: AST-120 treatment improved renal function, renal SSA, renal mitochondrial superoxide production, renal SOD expression, renal redox status by EPRI, and oxidative stress profiles by LDL-CMF, LPO and urinary HEL. Addition of indoxyl sulfate increased mitochondrial superoxide production and AST-120 also decreased this. Conclusions: Improvements in the redox status and lipid peroxidation induced by AST-120 may delay the progression of CKD.
机译:背景/目的:肾氧化还原状态的失衡导致肾功能不全的进展。我们使用慢性肾脏病(CKD)模型大鼠调查了口服木炭吸附剂(AST-120)对肾脏氧化还原状态,肾脏线粒体超氧化物产生和血清脂质过氧化的影响。方法:采用5/6肾切除术诱导CKD。 CKD大鼠分为两组:对照组和用AST-120治疗20周的组。我们评估:(1)通过体内低频电子自旋共振成像(EPRI)评估肾脏的氧化还原状态; (2)清除肾脏过氧化物的活性(SSA); (3)肾脏线粒体产生超氧化物; (4)对Cu-Zn超氧化物歧化酶(SOD)进行免疫染色,以及(5)氧化应激标志物,包括LDL负电荷(LDL-CMF),血清脂质过氧化物(LPO)和尿己酰赖氨酸(HEL)。还研究了尿毒症毒素吲哚酚硫酸盐对线粒体超氧化物生成的影响。结果:AST-120治疗改善了肾功能,肾脏SSA,肾脏线粒体超氧化物的产生,肾脏SOD表达,EPRI的肾脏氧化还原状态以及LDL-CMF,LPO和尿液HEL的氧化应激状况。硫酸吲哚酚的添加增加了线粒体超氧化物的产生,而AST-120也降低了这一点。结论:AST-120引起的氧化还原状态和脂质过氧化作用的改善可能延迟了CKD的进展。

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