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Antiepileptic Drugs and Their Dual Mechanism of Action on Carbonic Anhydrase
(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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9105189/ https://www.ncbi.nlm.nih.gov/pubmed/35566738 http://dx.doi.org/10.3390/jcm11092614 |
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author | Magheru, Calin Magheru, Sorina Coltau, Marcela Hoza, Anica Moldovan, Corina Sachelarie, Liliana Gradinaru, Irina Hurjui, Loredana Liliana Marc, Felicia Farcas, Dorina Maria |
author_facet | Magheru, Calin Magheru, Sorina Coltau, Marcela Hoza, Anica Moldovan, Corina Sachelarie, Liliana Gradinaru, Irina Hurjui, Loredana Liliana Marc, Felicia Farcas, Dorina Maria |
author_sort | Magheru, Calin |
collection | PubMed |
description | (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. |
format | Online Article Text |
id | pubmed-9105189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91051892022-05-14 Antiepileptic Drugs and Their Dual Mechanism of Action on Carbonic Anhydrase Magheru, Calin Magheru, Sorina Coltau, Marcela Hoza, Anica Moldovan, Corina Sachelarie, Liliana Gradinaru, Irina Hurjui, Loredana Liliana Marc, Felicia Farcas, Dorina Maria J Clin Med Article (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. MDPI 2022-05-06 /pmc/articles/PMC9105189/ /pubmed/35566738 http://dx.doi.org/10.3390/jcm11092614 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Magheru, Calin Magheru, Sorina Coltau, Marcela Hoza, Anica Moldovan, Corina Sachelarie, Liliana Gradinaru, Irina Hurjui, Loredana Liliana Marc, Felicia Farcas, Dorina Maria Antiepileptic Drugs and Their Dual Mechanism of Action on Carbonic Anhydrase |
title | Antiepileptic Drugs and Their Dual Mechanism of Action on Carbonic Anhydrase |
title_full | Antiepileptic Drugs and Their Dual Mechanism of Action on Carbonic Anhydrase |
title_fullStr | Antiepileptic Drugs and Their Dual Mechanism of Action on Carbonic Anhydrase |
title_full_unstemmed | Antiepileptic Drugs and Their Dual Mechanism of Action on Carbonic Anhydrase |
title_short | Antiepileptic Drugs and Their Dual Mechanism of Action on Carbonic Anhydrase |
title_sort | antiepileptic drugs and their dual mechanism of action on carbonic anhydrase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9105189/ https://www.ncbi.nlm.nih.gov/pubmed/35566738 http://dx.doi.org/10.3390/jcm11092614 |
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