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乙酰唑胺治疗特发性颅内高压。

Acetazolamide for the treatment of idiopathic intracranial hypertension.

作者信息

Supuran Claudiu T

机构信息

NEUROFARBA Department, Università degli Studi di Firenze, Polo Scientifico, Section of Pharmaceutical and Nutriceutical Sciences, Via Ugo Schiff 6, 50019 Sesto Fiorentino, Florence, Italy.

出版信息

Expert Rev Neurother. 2015;15(8):851-6. doi: 10.1586/14737175.2015.1066675. Epub 2015 Jul 7.

Abstract

Idiopathic intracranial hypertension (IIH) is characterized by an increase of intracranial pressure in the absence of neurologic tumors. The sulfonamide carbonic anhydrase (CA, EC 4.2.1.1) inhibitor (CAI) acetazolamide (AAZ), a compound developed in the 1950s as a diuretic drug and presently used as an antiglaucoma, antiepileptic and diuretic agent, is effective in the treatment of IIH. AAZ is a low nanomolar inhibitor of CA isoforms involved in cerebrospinal fluid (CSF) secretion. Inhibition of brain/choroid plexus CA II, IV, VA and XII leads to a decreased CSF fluid secretion and control of the intracranial pressure. Although many sulfonamide/sulfamate CAIs are in clinical use for decades, apparently only AAZ is being currently used clinically for IIH. We speculate that more lipophilic CAIs such as methazolamide, zonisamide or topiramate should lead to a more effective control of increased intracranial pressure, thus having the opportunity to become useful in the management of IIH.

摘要

特发性颅内高压(IIH)的特征是在无神经肿瘤的情况下颅内压升高。磺胺类碳酸酐酶(CA,EC 4.2.1.1)抑制剂(CAI)乙酰唑胺(AAZ)是20世纪50年代开发的一种利尿药,目前用作抗青光眼、抗癫痫和利尿药,对IIH的治疗有效。AAZ是参与脑脊液(CSF)分泌的CA同工型的低纳摩尔抑制剂。抑制脑/脉络丛CA II、IV、VA和XII会导致脑脊液分泌减少并控制颅内压。尽管许多磺胺类/氨基磺酸盐类CAI已临床使用数十年,但目前显然只有AAZ在临床上用于IIH。我们推测,更多亲脂性CAI,如甲醋唑胺、唑尼沙胺或托吡酯,应能更有效地控制颅内压升高,从而有机会在IIH的治疗中发挥作用。

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