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Theory-based analysis of clinical efficacy of triptans using receptor occupancy

BACKGROUND: Triptans, serotonin 5-HT(1B/1D) receptor agonists, exert their action by targeting serotonin 5-HT(1B/1D) receptors, are used for treatment of migraine attack. Presently, 5 different triptans, namely sumatriptan, zolmitriptan, eletriptan, rizatriptan, and naratriptan, are marketed in Japa...

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Detalles Bibliográficos
Autores principales: Tokuoka, Kentaro, Takayanagi, Risa, Suzuki, Yuji, Watanabe, Masayuki, Kitagawa, Yasuhisa, Yamada, Yasuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273730/
https://www.ncbi.nlm.nih.gov/pubmed/25488888
http://dx.doi.org/10.1186/1129-2377-15-85
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author Tokuoka, Kentaro
Takayanagi, Risa
Suzuki, Yuji
Watanabe, Masayuki
Kitagawa, Yasuhisa
Yamada, Yasuhiko
author_facet Tokuoka, Kentaro
Takayanagi, Risa
Suzuki, Yuji
Watanabe, Masayuki
Kitagawa, Yasuhisa
Yamada, Yasuhiko
author_sort Tokuoka, Kentaro
collection PubMed
description BACKGROUND: Triptans, serotonin 5-HT(1B/1D) receptor agonists, exert their action by targeting serotonin 5-HT(1B/1D) receptors, are used for treatment of migraine attack. Presently, 5 different triptans, namely sumatriptan, zolmitriptan, eletriptan, rizatriptan, and naratriptan, are marketed in Japan. In the present study, we retrospectively analyzed the relationships of clinical efficacy (headache relief) in Japanese and 5-HT(1B/1D) receptor occupancy (Φ(1B) and Φ(1D)). Receptor occupancies were calculated from both the pharmacokinetic and pharmacodynamic data of triptans. METHODS: To evaluate the total amount of exposure to drug, we calculated the area under the plasma concentration-time curve (AUC(cp)) and the areas under the time curves for Ф(1B) and Ф(1D) (AUC(Ф)(1B) and AUC(Ф)(1D)). Moreover, parameters expressing drug transfer and binding rates (A( cp ), A( Ф )( 1B ), A( Ф )( 1D )) were calculated. RESULTS: Our calculations showed that Ф(max)(1B) and Ф(max)(1D) were relatively high at 32.0-89.4% and 68.4-96.2%, respectively, suggesting that it is likely that a high occupancy is necessary to attain the clinical effect. In addition, the relationships between therapeutic effect and AUC(cp), AUC(Φ)(1B), AUC(Φ)(1D), and A( cp ) · AUC(cp) differed with each drug and administered form, whereas a significant relationship was found between the therapeutic effect and A( Φ )( 1B ) · AUC(Φ)(1B) or A( Φ )( 1D ) · AUC(Φ)(1D) that was not affected by the drug and the form of administration. CONCLUSIONS: These results suggest that receptor occupancy can be used as a parameter for a common index to evaluate the therapeutic effect. We considered that the present findings provide useful information to support the proper use of triptans.
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spelling pubmed-42737302015-01-15 Theory-based analysis of clinical efficacy of triptans using receptor occupancy Tokuoka, Kentaro Takayanagi, Risa Suzuki, Yuji Watanabe, Masayuki Kitagawa, Yasuhisa Yamada, Yasuhiko J Headache Pain Research Article BACKGROUND: Triptans, serotonin 5-HT(1B/1D) receptor agonists, exert their action by targeting serotonin 5-HT(1B/1D) receptors, are used for treatment of migraine attack. Presently, 5 different triptans, namely sumatriptan, zolmitriptan, eletriptan, rizatriptan, and naratriptan, are marketed in Japan. In the present study, we retrospectively analyzed the relationships of clinical efficacy (headache relief) in Japanese and 5-HT(1B/1D) receptor occupancy (Φ(1B) and Φ(1D)). Receptor occupancies were calculated from both the pharmacokinetic and pharmacodynamic data of triptans. METHODS: To evaluate the total amount of exposure to drug, we calculated the area under the plasma concentration-time curve (AUC(cp)) and the areas under the time curves for Ф(1B) and Ф(1D) (AUC(Ф)(1B) and AUC(Ф)(1D)). Moreover, parameters expressing drug transfer and binding rates (A( cp ), A( Ф )( 1B ), A( Ф )( 1D )) were calculated. RESULTS: Our calculations showed that Ф(max)(1B) and Ф(max)(1D) were relatively high at 32.0-89.4% and 68.4-96.2%, respectively, suggesting that it is likely that a high occupancy is necessary to attain the clinical effect. In addition, the relationships between therapeutic effect and AUC(cp), AUC(Φ)(1B), AUC(Φ)(1D), and A( cp ) · AUC(cp) differed with each drug and administered form, whereas a significant relationship was found between the therapeutic effect and A( Φ )( 1B ) · AUC(Φ)(1B) or A( Φ )( 1D ) · AUC(Φ)(1D) that was not affected by the drug and the form of administration. CONCLUSIONS: These results suggest that receptor occupancy can be used as a parameter for a common index to evaluate the therapeutic effect. We considered that the present findings provide useful information to support the proper use of triptans. Springer 2014-12-08 /pmc/articles/PMC4273730/ /pubmed/25488888 http://dx.doi.org/10.1186/1129-2377-15-85 Text en Copyright © 2014 Tokuoka et al.; licensee Springer. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Tokuoka, Kentaro
Takayanagi, Risa
Suzuki, Yuji
Watanabe, Masayuki
Kitagawa, Yasuhisa
Yamada, Yasuhiko
Theory-based analysis of clinical efficacy of triptans using receptor occupancy
title Theory-based analysis of clinical efficacy of triptans using receptor occupancy
title_full Theory-based analysis of clinical efficacy of triptans using receptor occupancy
title_fullStr Theory-based analysis of clinical efficacy of triptans using receptor occupancy
title_full_unstemmed Theory-based analysis of clinical efficacy of triptans using receptor occupancy
title_short Theory-based analysis of clinical efficacy of triptans using receptor occupancy
title_sort theory-based analysis of clinical efficacy of triptans using receptor occupancy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273730/
https://www.ncbi.nlm.nih.gov/pubmed/25488888
http://dx.doi.org/10.1186/1129-2377-15-85
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