Verkoelen C F, Romijn J C
Urol Res. 1996;24(4):183-91. doi: 10.1007/BF00295891.
Hyperoxaluria is considered to play a crucial role in calcium oxalate (CaOx) renal stone disease. The amount of oxalate excreted into the urine depends on intestinal absorption, endogenous production, renal clearance and renal tubular transport. Since a primary disorder has not been found so far in most CaOx stone formers and since oxalate is freely filtered at the glomerulus, most studies are presently focussed on alterations in epithelial oxalate transport pathways. Oxalate can be transported across an epithelium by the paracellular (passive) and transcellular (active) pathway. Oxalate transport across cellular membranes is mediated by anion-exchange transport proteins. A defect in the structure of these transport proteins could explain augmented transcellular oxalate transport. Little is known about the physiological regulation of oxalate transport. In this review cellular transport systems for oxalate will be summarized with special attention for the progress that has been made to study oxalate transport in a model of cultured renal tubule cells. Better understanding of the physiological processes that are involved in oxalate transport could yield information on the basis of which it might be possible to design new approaches for an effective treatment of CaOx stone disease.
高草酸尿症被认为在草酸钙肾结石疾病中起关键作用。排泄到尿液中的草酸盐量取决于肠道吸收、内源性生成、肾脏清除和肾小管转运。由于目前在大多数草酸钙结石形成者中尚未发现原发性疾病,且草酸盐在肾小球可自由滤过,因此目前大多数研究集中在上皮细胞草酸盐转运途径的改变上。草酸盐可通过细胞旁(被动)和跨细胞(主动)途径跨上皮细胞转运。草酸盐跨细胞膜的转运由阴离子交换转运蛋白介导。这些转运蛋白结构的缺陷可能解释跨细胞草酸盐转运增加的原因。关于草酸盐转运的生理调节知之甚少。在这篇综述中,将总结草酸盐的细胞转运系统,并特别关注在培养的肾小管细胞模型中研究草酸盐转运所取得的进展。更好地理解草酸盐转运所涉及的生理过程可能会产生相关信息,在此基础上有可能设计出新的方法来有效治疗草酸钙结石疾病。