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A comprehensive review on pharmacological applications and drug-induced toxicity of valproic acid

Valproic acid, a branching short chain fatty acid, is a popular drug to treat epilepsy and acts as a mood-stabilizing drug. The obstruction of ion channels and Gamma Amino Butyrate transamino butyrate GABA has been linked to antiepileptic effects. Valproic acid has been characterized as a Histone de...

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Autores principales: Safdar, Ayesha, Ismail, Fatima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023552/
https://www.ncbi.nlm.nih.gov/pubmed/36942277
http://dx.doi.org/10.1016/j.jsps.2022.12.001
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author Safdar, Ayesha
Ismail, Fatima
author_facet Safdar, Ayesha
Ismail, Fatima
author_sort Safdar, Ayesha
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description Valproic acid, a branching short chain fatty acid, is a popular drug to treat epilepsy and acts as a mood-stabilizing drug. The obstruction of ion channels and Gamma Amino Butyrate transamino butyrate GABA has been linked to antiepileptic effects. Valproic acid has been characterized as a Histone deacetylase inhibitor, functioning directly transcription of gene levels by blocking the deacetylation of histones and increasing the accessibility of transcription sites. Study has been extensively focused on pharmaceutical activity of valproic acid through various pharmacodynamics activity from absorption, distribution and excretion particularly in patients who are resistant to or intolerant of lithium or carbamazepine, as well as those with mixed mania or rapid cycling.
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spelling pubmed-100235522023-03-19 A comprehensive review on pharmacological applications and drug-induced toxicity of valproic acid Safdar, Ayesha Ismail, Fatima Saudi Pharm J Review Valproic acid, a branching short chain fatty acid, is a popular drug to treat epilepsy and acts as a mood-stabilizing drug. The obstruction of ion channels and Gamma Amino Butyrate transamino butyrate GABA has been linked to antiepileptic effects. Valproic acid has been characterized as a Histone deacetylase inhibitor, functioning directly transcription of gene levels by blocking the deacetylation of histones and increasing the accessibility of transcription sites. Study has been extensively focused on pharmaceutical activity of valproic acid through various pharmacodynamics activity from absorption, distribution and excretion particularly in patients who are resistant to or intolerant of lithium or carbamazepine, as well as those with mixed mania or rapid cycling. Elsevier 2023-02 2022-12-09 /pmc/articles/PMC10023552/ /pubmed/36942277 http://dx.doi.org/10.1016/j.jsps.2022.12.001 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Safdar, Ayesha
Ismail, Fatima
A comprehensive review on pharmacological applications and drug-induced toxicity of valproic acid
title A comprehensive review on pharmacological applications and drug-induced toxicity of valproic acid
title_full A comprehensive review on pharmacological applications and drug-induced toxicity of valproic acid
title_fullStr A comprehensive review on pharmacological applications and drug-induced toxicity of valproic acid
title_full_unstemmed A comprehensive review on pharmacological applications and drug-induced toxicity of valproic acid
title_short A comprehensive review on pharmacological applications and drug-induced toxicity of valproic acid
title_sort comprehensive review on pharmacological applications and drug-induced toxicity of valproic acid
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023552/
https://www.ncbi.nlm.nih.gov/pubmed/36942277
http://dx.doi.org/10.1016/j.jsps.2022.12.001
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