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草酸钙尿结石晶体生长抑制剂。

Urinary calcium oxalate crystal growth inhibitors.

作者信息

Worcester E M

机构信息

Department of Medicine, Department of Veterans Affairs Medical Center, Milwaukee, WI 53295.

出版信息

J Am Soc Nephrol. 1994 Nov;5(5 Suppl 1):S46-53. doi: 10.1681/ASN.V55s46.

DOI:10.1681/ASN.V55s46
PMID:7873744
Abstract

Calcium stones occur because renal tubular fluid and urine are supersaturated with respect to calcium oxalate and phosphate. The process of stone formation includes crystal nucleation, growth, aggregation, and attachment to renal epithelia. Urine contains macromolecules that modify these processes and may protect against stone formation. Attention has focused especially on inhibitors of crystal growth, and several have been isolated from urine, including nephrocalcin, an acidic phosphorylated glycoprotein that contains several residues of gamma-carboxyglutamic acid per molecule; osteopontin (uropontin), a phosphorylated glycoprotein also found in bone matrix; uronic acid-rich protein, which contains a covalently bound glycosaminoglycan residue; and several others. Abnormalities in structure and/or function have been detected in some of these proteins in stone formers' urine. However, the overall ability of urinary macromolecules to inhibit calcium oxalate crystal growth is often normal in stone formers. Recently, attention has been focused on the ability of these molecules to inhibit other stages in stone formation. Nephrocalcin can inhibit crystal nucleation, for example, and both nephrocalcin and Tamm-Horsfall protein inhibit crystal aggregation. Nephrocalcin and Tamm-Horsfall protein from stone formers are less active in preventing aggregation, and under some conditions, Tamm-Horsfall protein may promote the formation of crystal aggregates, especially in the presence of high concentrations of calcium. The structural abnormalities responsible for impaired inhibitory activity are not completely understood.

摘要

钙结石的形成是因为肾小管液和尿液中的草酸钙和磷酸盐处于过饱和状态。结石形成的过程包括晶体成核、生长、聚集以及附着于肾上皮细胞。尿液中含有可改变这些过程并可能预防结石形成的大分子物质。人们尤其关注晶体生长抑制剂,并且已经从尿液中分离出了几种,包括肾钙素,一种酸性磷酸化糖蛋白,每个分子含有几个γ-羧基谷氨酸残基;骨桥蛋白(尿桥蛋白),一种也存在于骨基质中的磷酸化糖蛋白;富含糖醛酸的蛋白,其含有一个共价结合的糖胺聚糖残基;以及其他几种。在结石患者的尿液中,已检测到其中一些蛋白质的结构和/或功能异常。然而,结石患者尿液中大分子物质抑制草酸钙晶体生长的总体能力通常是正常的。最近,人们的注意力集中在这些分子抑制结石形成其他阶段的能力上。例如,肾钙素可以抑制晶体成核,肾钙素和Tamm-Horsfall蛋白都可以抑制晶体聚集。结石患者的肾钙素和Tamm-Horsfall蛋白在防止聚集方面活性较低,并且在某些情况下,Tamm-Horsfall蛋白可能促进晶体聚集体的形成,尤其是在高钙浓度存在的情况下。导致抑制活性受损的结构异常尚未完全了解。

相似文献

1
Urinary calcium oxalate crystal growth inhibitors.草酸钙尿结石晶体生长抑制剂。
J Am Soc Nephrol. 1994 Nov;5(5 Suppl 1):S46-53. doi: 10.1681/ASN.V55s46.
2
Inhibitors of stone formation.结石形成抑制剂。
Semin Nephrol. 1996 Sep;16(5):474-86.
3
Glycoprotein calcium oxalate crystal growth inhibitor in urine.尿液中的糖蛋白草酸钙晶体生长抑制剂。
Miner Electrolyte Metab. 1987;13(4):267-72.
4
[Glycoprotein inhibitors of urinary calculi formation].
Nephrologie. 1993;14(4):183-7.
5
Isolation from human calcium oxalate renal stones of nephrocalcin, a glycoprotein inhibitor of calcium oxalate crystal growth. Evidence that nephrocalcin from patients with calcium oxalate nephrolithiasis is deficient in gamma-carboxyglutamic acid.从人草酸钙肾结石中分离出肾钙蛋白,一种草酸钙晶体生长的糖蛋白抑制剂。草酸钙肾结石患者的肾钙蛋白缺乏γ-羧基谷氨酸的证据。
J Clin Invest. 1987 Jun;79(6):1782-7. doi: 10.1172/JCI113019.
6
Role of nephrocalcin in inhibition of calcium oxalate crystallization and nephrolithiasis.肾钙素在抑制草酸钙结晶和肾结石形成中的作用。
Miner Electrolyte Metab. 1994;20(6):378-84.
7
Protein inhibitors of crystal growth.
J Urol. 1989 Mar;141(3 Pt 2):750-2. doi: 10.1016/s0022-5347(17)41001-9.
8
[Uronic-acid-rich protein: a new glycoprotein inhibiting the crystallization of calcium oxalate in vitro].富含糖醛酸的蛋白质:一种新型糖蛋白在体外抑制草酸钙结晶
Nephrologie. 1996;17(3):157-62.
9
Defective urinary crystallization inhibition and urinary stone formation.尿结晶抑制缺陷与尿路结石形成。
Int Braz J Urol. 2006 May-Jun;32(3):342-8; discussion 349. doi: 10.1590/s1677-55382006000300016.
10
Inhibition of calcium oxalate monohydrate crystal aggregation by urine proteins.尿蛋白对一水合草酸钙晶体聚集的抑制作用。
Am J Physiol. 1989 Jul;257(1 Pt 2):F99-106. doi: 10.1152/ajprenal.1989.257.1.F99.

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PLoS One. 2016 Sep 20;11(9):e0162600. doi: 10.1371/journal.pone.0162600. eCollection 2016.
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