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The Renal Effects of Vanadate Exposure! Potential Biomarkers and Oxidative Stress as a Mechanism of Functional Renal Disorders-Preliminary Studies

机译:钒酸盐暴露的肾脏效应!潜在的生物标志物和氧化应激作为功能性肾脏疾病的机制-初步研究

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摘要

The alterations in the levels/activities of selected biomarkers for detecting kidney toxicity and in the levels of some oxidative stress (OS) markers and elements were studied in male rats to evaluate biochemically the degree of kidney damage, investigate the role of OS in the mechanism of functional renal disorders, reveal potential biomarkers of renal function, and assess the renal mineral changes in the conditions of a 12-week sodium metavanadate (SMV, 0.125 mgV/mL) exposure. The results showed that OS is involved in the mechanism underlying the development of SMV-induced functional renal disturbances. They also suggest that the urinary cystatin C (CysC_u) and kidney injury molecule-1 (KIM-1_u) could be the most appropriate to evaluate renal function at the conditions of SMV intoxication when the fluid intake, excreted urinary volume (EUV), body weight (BW), and the urinary creatinine excretion (Cre_u) decreased. The use of such tests as the urinary lactate dehydrogenase, alkaline phosphatase, gamma-glutamyltranspeptidase, and N-acetyl-beta-D-glucosaminidase (LDH_u, ALP_u, GGTP_u, and NAG_u) seems not to be valid given their reduced activities. The use of only traditional biomarkers of renal function in these conditions may, in turn, be insufficient because their alterations are greatly influenced by the changes in the fluid intake and/or BW.
机译:在雄性大鼠中研究了选择的用于检测肾脏毒性的生物标记物的水平/活性和某些氧化应激(OS)标记物和元素的水平变化,以生化评估肾脏损伤的程度,研究OS在该机制中的作用的功能性肾脏疾病,揭示肾脏功能的潜在生物标志物以及评估在12周偏钒酸钠(SMV,0.125 mgV / mL)暴露条件下肾脏矿物质的变化。结果表明OS参与了SMV诱发的功能性肾功能障碍发展的潜在机制。他们还建议,在体液摄入,排尿量(EUV),体液摄入,SMV中毒的情况下,尿半胱氨酸蛋白酶抑制剂C(CysC_u)和肾损伤分子1(KIM-1_u)最适合评估肾功能。体重(BW)和尿肌酐排泄(Cre_u)减少。鉴于尿液乳酸脱氢酶,碱性磷酸酶,γ-谷氨酰转肽酶和N-乙酰基-β-D-氨基葡萄糖苷酶(LDH_u,ALP_u,GGTP_u和NAG_u)的活性降低,因此似乎无效。在这些情况下,仅使用传统的肾功能生物标志物可能反过来可能是不够的,因为它们的改变很大程度上受液体摄入量和/或体重的变化影响。

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