Magheru Calin, Magheru Sorina, Coltau Marcela, Hoza Anica, Moldovan Corina, Sachelarie Liliana, Gradinaru Irina, Hurjui Loredana Liliana, Marc Felicia, Farcas Dorina Maria
Department of Medical Disciplines, Faculty of Medicine and Pharmacy, University of Oradea, 410073 Oradea, Romania.
City Hospital Prof. Dr. Ioan Puscas Simleu Silvaniei, 455300 Simleu Silvaniei, Romania.
J Clin Med. 2022 May 6;11(9):2614. doi: 10.3390/jcm11092614.
(1) Background: The benefit of using inhibitors of carbonic anhydrase (CA), such as acetazolamide, in the treatment of epilepsy has previously been described. (2) Methods: In this paper, the effect on CA of the most well-known antiepileptic drugs was studied in vitro and in vivo. The effects, after chronic treatment, of carbamazepine, phenytoin, valproate, primidone, clonazepam, and ethosuximide were studied in vitro on purified CA, isozyme I (CA I) and CA, and isozyme II (CA II) activity and in vivo on epileptic erythrocyte CA I and CA II activity. (3) Results: In vitro results showed that all antiepileptic drugs reduced purified CA II activity according to dose-response relationships and slightly inhibited CA I activity. In vivo results showed that the chronic administration of antiseizure drugs induced a progressive reduction in erythrocyte CA II activity in all the groups studied. This study shows that CA II inhibition can be induced both in vitro and in vivo by major antiepileptic agents as it might be one of the effective mechanisms of these anticonvulsant drugs. (4) Conclusions: The decrease in CA II activity in epileptic patients after antiseizure treatment suggests the involvement of CA II in the pathogenesis of epilepsy.
(1) 背景:此前已有文献描述使用碳酸酐酶(CA)抑制剂(如乙酰唑胺)治疗癫痫的益处。(2) 方法:本文在体外和体内研究了最知名的抗癫痫药物对CA的影响。在体外研究了卡马西平、苯妥英、丙戊酸、扑米酮、氯硝西泮和乙琥胺长期治疗后对纯化的CA同工酶I(CA I)和CA同工酶II(CA II)活性的影响,在体内研究了对癫痫患者红细胞CA I和CA II活性的影响。(3) 结果:体外研究结果表明,所有抗癫痫药物均根据剂量反应关系降低了纯化的CA II活性,并轻微抑制了CA I活性。体内研究结果表明,在所有研究组中,长期服用抗癫痫药物均导致红细胞CA II活性逐渐降低。本研究表明,主要抗癫痫药物在体外和体内均可诱导CA II抑制,这可能是这些抗惊厥药物的有效作用机制之一。(4) 结论:抗癫痫治疗后癫痫患者CA II活性降低表明CA II参与了癫痫的发病机制。