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Ciclosporin 10 years on: indications and efficacy

Ciclosporin is a lipophilic cyclic polypeptide with powerful immunosuppressive and immunomodulatory properties that has been used in veterinary medicine for two decades. It is a calcineurin inhibitor whose principal mode of action is to inhibit T cell activation. The drug is principally absorbed fro...

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Detalles Bibliográficos
Autores principales: Forsythe, Peter, Paterson, Sue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995292/
https://www.ncbi.nlm.nih.gov/pubmed/24682697
http://dx.doi.org/10.1136/vr.102484
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author Forsythe, Peter
Paterson, Sue
author_facet Forsythe, Peter
Paterson, Sue
author_sort Forsythe, Peter
collection PubMed
description Ciclosporin is a lipophilic cyclic polypeptide with powerful immunosuppressive and immunomodulatory properties that has been used in veterinary medicine for two decades. It is a calcineurin inhibitor whose principal mode of action is to inhibit T cell activation. The drug is principally absorbed from the small intestine and is metabolised in the intestine and liver by the cytochrome P450 enzyme system. Ciclosporin is known to interact with a wide range of pharmacological agents. Numerous studies have demonstrated good efficacy for the management of canine atopic dermatitis and this has been a licensed indication since 2003. In addition to the treatment of atopic dermatitis, it has been used as an aid in the management of numerous other dermatological conditions in animals including perianal fistulation, sebaceous adenitis, pododermatitis, chronic otitis externa and pemphigus foliaceus. This article reviews the mode of action, pharmacokinetics, indications for use and efficacy of ciclosporin in veterinary dermatology.
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spelling pubmed-39952922014-04-30 Ciclosporin 10 years on: indications and efficacy Forsythe, Peter Paterson, Sue Vet Rec Review Ciclosporin is a lipophilic cyclic polypeptide with powerful immunosuppressive and immunomodulatory properties that has been used in veterinary medicine for two decades. It is a calcineurin inhibitor whose principal mode of action is to inhibit T cell activation. The drug is principally absorbed from the small intestine and is metabolised in the intestine and liver by the cytochrome P450 enzyme system. Ciclosporin is known to interact with a wide range of pharmacological agents. Numerous studies have demonstrated good efficacy for the management of canine atopic dermatitis and this has been a licensed indication since 2003. In addition to the treatment of atopic dermatitis, it has been used as an aid in the management of numerous other dermatological conditions in animals including perianal fistulation, sebaceous adenitis, pododermatitis, chronic otitis externa and pemphigus foliaceus. This article reviews the mode of action, pharmacokinetics, indications for use and efficacy of ciclosporin in veterinary dermatology. BMJ Group 2014-03 /pmc/articles/PMC3995292/ /pubmed/24682697 http://dx.doi.org/10.1136/vr.102484 Text en British Veterinary Association This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Review
Forsythe, Peter
Paterson, Sue
Ciclosporin 10 years on: indications and efficacy
title Ciclosporin 10 years on: indications and efficacy
title_full Ciclosporin 10 years on: indications and efficacy
title_fullStr Ciclosporin 10 years on: indications and efficacy
title_full_unstemmed Ciclosporin 10 years on: indications and efficacy
title_short Ciclosporin 10 years on: indications and efficacy
title_sort ciclosporin 10 years on: indications and efficacy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995292/
https://www.ncbi.nlm.nih.gov/pubmed/24682697
http://dx.doi.org/10.1136/vr.102484
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