Thiry Anne, Dogné Jean-Michel, Supuran Claudiu T, Masereel Bernard
Drug Design and Discovery Center, FUNDP, University of Namur, Namur, Belgium.
Curr Top Med Chem. 2007;7(9):855-64. doi: 10.2174/156802607780636726.
Seizures are one of the most common neurological disorders in clinical medicine. Triggering mechanisms by which seizures form remain unclear, but are related to a rapid change in ionic composition, including an increase of intracellular potassium concentration and pH shifts within the brain. pH buffering of extra- and intracellular spaces is mainly carried out by the CO(2)/ HCO(3)(-) buffer, the equilibration of the two species being assured by the zinc enzyme carbonic anhydrase (CA, EC 4.2.1.1). Some carbonic anhydrase inhibitors (CAIs) are used as anticonvulsants in the treatment of epilepsy. In this review, we will describe the link between CA and seizures on the basis of several putative mechanisms. Several CA isozymes have been pointed out for their contribution to epileptiform activity. An overview of the CA isozyme expression in the brain and of their specifics roles is also discussed. This article reviews the research achievements published on CA inhibitors, clinically used as anticonvulsant and those under development.
癫痫发作是临床医学中最常见的神经系统疾病之一。癫痫发作形成的触发机制尚不清楚,但与离子组成的快速变化有关,包括细胞内钾浓度的增加和脑内pH值的变化。细胞外和细胞内空间的pH缓冲主要由CO(2)/HCO(3)(-)缓冲系统完成,这两种物质的平衡由锌酶碳酸酐酶(CA,EC 4.2.1.1)保证。一些碳酸酐酶抑制剂(CAIs)在癫痫治疗中用作抗惊厥药。在这篇综述中,我们将基于几种假定机制描述CA与癫痫发作之间的联系。已经指出几种CA同工酶对癫痫样活动有贡献。还讨论了CA同工酶在脑中的表达概况及其具体作用。本文综述了已发表的关于用作抗惊厥药的CA抑制剂以及正在开发的CA抑制剂的研究成果。