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草酸钙结石抑制剂:其相互作用对草酸钙结晶的影响。

Inhibitors of oxalocalcic lithiasis: effects of their interactions on calcium oxalate crystallization.

机构信息

Centre Grup de Tècniques de Separació en Química, Química Analítica, Departament de Química, Universitat Autònoma de Barcelona, Bellaterra 08193, Spain.

出版信息

Urology. 2012 Nov;80(5):1163.e13-8. doi: 10.1016/j.urology.2012.04.040. Epub 2012 Jun 27.

Abstract

OBJECTIVE

To study the possible effects caused by the interaction of some urinary components on the inhibition of calcium oxalate crystallization. Such interactions are susceptible to importantly change the inhibitory behavior of some urinary components by producing either positive (synergistic) or negative effects on preventing crystallization.

METHODS

A urinary lithogenic risk (ULR) test was used to follow the crystallization of calcium oxalate from artificial urine in the presence of binary mixtures of known inhibitors of its crystallization (phytate, pyrophosphate, citrate, and chondroitin sulfate), which were assayed in physiological concentrations.

RESULTS

Only the mixtures phytate + pyrophosphate and phytate + citrate manifested interaction effects on the calcium oxalate crystallization. Although the former exhibited synergistic effects, the latter showed negative effects on the inhibition. These effects are explained in terms of the affinity of the inhibitors for the calcium oxalate crystals surface and their concentrations in urine.

CONCLUSION

The crystallization inhibitory capacity of target urine is explained by the combined effect of the compounds present in the complex urine matrix rather than the individual action of each compound. This kind of interactions is of key value in designing prophylactic treatments of urolithiasis based on inhibitors intake.

摘要

目的

研究一些尿成分相互作用对抑制草酸钙结晶可能产生的影响。这种相互作用可能会通过产生正(协同)或负(拮抗)效应对结晶抑制产生重要影响,从而显著改变一些尿成分的抑制行为。

方法

采用尿结石形成风险(ULR)试验,在已知的结晶抑制剂(植酸、焦磷酸盐、柠檬酸盐和硫酸软骨素)的二元混合物存在的情况下,从人工尿液中跟踪草酸钙的结晶,这些抑制剂以生理浓度进行检测。

结果

只有植酸盐+焦磷酸盐和植酸盐+柠檬酸盐这两种混合物对草酸钙结晶表现出相互作用效应。虽然前者表现出协同效应,但后者对抑制作用表现出负效应。这些效应可以根据抑制剂对草酸钙晶体表面的亲和力及其在尿液中的浓度来解释。

结论

目标尿液的结晶抑制能力是由复杂尿液基质中存在的化合物的综合效应解释的,而不是每个化合物的单独作用。这种相互作用在基于抑制剂摄入设计尿石症预防治疗方面具有关键价值。

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