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乳酸脱氢酶 5:鉴定一个可成药的靶点以减少草酸尿。

Lactate dehydrogenase 5: identification of a druggable target to reduce oxaluria.

出版信息

J Clin Invest. 2019 May 20;129(6):2201-2204. doi: 10.1172/JCI128709.

Abstract

Excessive excretion of oxalate in the urine results in the formation of calcium oxalate crystals and subsequent kidney stone formation. Severe forms of hyperoxaluria, including genetic forms and those that result from ethylene glycol poisoning, can result in end-stage renal disease. Therapeutic interventions are limited and often rely on dietary intervention. In this issue of the JCI, Le Dudal and colleagues demonstrate that the lactate dehydrogenase 5 inhibitor (LDH5) stiripentol reduces urinary oxalate excretion. Importantly, stiripentol treatment of a single individual with primary hyperoxaluria reduced the urinary oxalate excretion. Together, these results support further evaluation of LDH5 as a therapeutic target for hyperoxaluria.

摘要

尿中草酸盐排泄过多会导致草酸钙晶体形成,并随后形成肾结石。包括遗传形式和乙二醇中毒引起的严重高草酸尿症会导致终末期肾病。治疗干预措施有限,通常依赖于饮食干预。在本期 JCI 中,Le Dudal 及其同事证明,乳酸脱氢酶 5 抑制剂(LDH5)司替戊醇可减少尿草酸盐排泄。重要的是,司替戊醇治疗一名原发性高草酸尿症患者可降低尿草酸盐排泄。这些结果共同支持进一步评估 LDH5 作为高草酸尿症的治疗靶点。

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[Effect of stiripentol on urine oxalate excretion].[司替戊醇对尿草酸排泄的影响]
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Stiripentol identifies a therapeutic target to reduce oxaluria.司替戊醇确定了一个治疗靶点以减少草酸尿。
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本文引用的文献

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Novel therapeutic approaches in primary hyperoxaluria.原发性高草酸尿症的新治疗方法。
Expert Opin Emerg Drugs. 2018 Dec;23(4):349-357. doi: 10.1080/14728214.2018.1552940. Epub 2018 Dec 12.
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Characterization of renal NaCl and oxalate transport in Slc26a6 mice.Slc26a6 小鼠肾 NaCl 和草酸盐转运的特征。
Am J Physiol Renal Physiol. 2019 Jan 1;316(1):F128-F133. doi: 10.1152/ajprenal.00309.2018. Epub 2018 Nov 14.
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Lactate in the brain: from metabolic end-product to signalling molecule.脑内乳酸:从代谢终产物到信号分子。
Nat Rev Neurosci. 2018 Apr;19(4):235-249. doi: 10.1038/nrn.2018.19. Epub 2018 Mar 8.
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Mutations in SLC26A1 Cause Nephrolithiasis.SLC26A1基因的突变导致肾结石。
Am J Hum Genet. 2016 Jun 2;98(6):1228-1234. doi: 10.1016/j.ajhg.2016.03.026. Epub 2016 May 19.

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