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Urinary factors affecting renal stone disease.

机译:影响肾结石疾病的泌尿因子。

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摘要

This study investigates the physicochemical aspects of calcium oxalate (CaOx) crystallization by the mixed suspension mixed product removal (MSMPR) system -- a continuous crystallization system. Total urinary glycoproteins (GPs) were shown to promote CaOx crystallization. Although whole urinary glycosaminoglyans (GAGs) showed no significant differences on CaOx crystallization, individual GAGs showed that chondroitin sulphate and heparan sulphate promoted the CaOx crystallization while hyaluronan (HA) promoted the formation of smaller CaOx crystals.;Active stone-former (SF) and post-treated SF groups had lower total urinary GAGs excretion but increased proportion of urinary HA than that of the normal controls indicating that urinary GAGs and HA are probably protective/risk factors for the occurrence and recurrence of renal stone disease.;This study suggested the possible events during subclinical CaOx renal stone disease. HA was secreted during CaOx induced cell injury and the injured cells will also secrete IL-1beta as the inflammatory cytokine. This can eventually lead to further HA secretion as well as CD44 expression (HA receptor) that can interact with the HA being secreted for CaOx crystal attachment and retention for stone formation.;Melamine renal stone disease incident in Chinese infants in late 2007 lead to the concern on how melamine affected renal stone disease. The physicochemical nature of melamine in urine was studied by the MSMPR system. Melamine was found to crystallize in normal acidic urinary pH (pH 6.0) and interacted with other lithogenic salts. Presence of melamine significantly enhanced the precipitation of calcium oxalate while the presence of uric acid significantly reduced melamine crystallization.;The main pathogen of urinary tract infection (UTI) -- E. coli on melamine crystallization that common in children was studied and found that it promotes melamine crystallization.;Currently prescribed therapeutic agents including potassium citrate and sodium bicarbonate on melamine crystallization were investigated and found that both of them did significantly reduce melamine crystallization.;Shi Wei is one of the Traditional Chinese medicines (TCM) used for treating renal stones. This study showed that human urine after Shi Wei supplementation had significant acute inhibitory effect on melamine crystallization but the effect was diminished or even levelled off after 1 week supplementation.
机译:这项研究调查了通过混合悬浮液混合产物去除(MSMPR)系统(连续结晶系统)进行草酸钙(CaOx)结晶的物理化学方面。总尿糖蛋白(GPs)可以促进CaOx结晶。尽管全尿糖胺聚糖(GAG)在CaOx结晶上没有显着差异,但个别GAGs显示硫酸软骨素和硫酸乙酰肝素促进了CaOx结晶,而透明质酸(HA)促进了较小的CaOx晶体的形成。 SF组经过治疗后的总尿GAGs排泄量较低,但尿中HA的比例高于正常对照组,这表明尿GAG和HA可能是肾结石疾病发生和复发的保护/危险因素。亚临床CaOx肾结石疾病期间可能发生的事件。在CaOx诱导的细胞损伤过程中会分泌HA,受损的细胞还将分泌IL-1β作为炎症性细胞因子。这最终可能导致进一步的HA分泌以及CD44表达(HA受体),该CD44表达(HA受体)可以与HA相互作用,从而引起CaOx晶体附着和保留以形成结石。2007年末中国婴儿发生的三聚氰胺肾结石导致关注三聚氰胺如何影响肾结石疾病。通过MSMPR系统研究了尿液中三聚氰胺的理化性质。发现三聚氰胺在正常的酸性尿液pH(pH 6.0)中结晶,并与其他成岩盐相互作用。三聚氰胺的存在显着增强了草酸钙的沉淀,而尿酸的存在则显着降低了三聚氰胺的结晶。研究了尿路感染(UTI)的主要病原菌-儿童常见的三聚氰胺结晶对大肠杆菌的影响,发现促进三聚氰胺的结晶。;目前研究的治疗剂包括柠檬酸钾和碳酸氢钠对三聚氰胺的结晶,发现它们均能显着降低三聚氰胺的结晶。;石薇是用于治疗肾结石的中药之一。 。这项研究表明,补充石Wei后的人尿对三聚氰胺的结晶具有明显的急性抑制作用,但在补充1周后这种作用减弱或趋于平稳。

著录项

  • 作者

    Poon, Ngork Wah.;

  • 作者单位

    Hong Kong Polytechnic University (Hong Kong).;

  • 授予单位 Hong Kong Polytechnic University (Hong Kong).;
  • 学科 Pathology.;Physical chemistry.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 241 p.
  • 总页数 241
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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