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Taltirelin is a superagonist at the human thyrotropin-releasing hormone receptor

Taltirelin (TAL) is a thyrotropin-releasing hormone (TRH) analog that is approved for use in humans in Japan. In this study, we characterized TAL binding to and signaling by the human TRH receptor (TRH-R) in a model cell system. We found that TAL exhibited lower binding affinities than TRH and lower...

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Autores principales: Thirunarayanan, Nanthakumar, Raaka, Bruce M., Gershengorn, Marvin C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3466466/
https://www.ncbi.nlm.nih.gov/pubmed/23087672
http://dx.doi.org/10.3389/fendo.2012.00120
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author Thirunarayanan, Nanthakumar
Raaka, Bruce M.
Gershengorn, Marvin C.
author_facet Thirunarayanan, Nanthakumar
Raaka, Bruce M.
Gershengorn, Marvin C.
author_sort Thirunarayanan, Nanthakumar
collection PubMed
description Taltirelin (TAL) is a thyrotropin-releasing hormone (TRH) analog that is approved for use in humans in Japan. In this study, we characterized TAL binding to and signaling by the human TRH receptor (TRH-R) in a model cell system. We found that TAL exhibited lower binding affinities than TRH and lower signaling potency via the inositol-1,4,5-trisphosphate/calcium pathway than TRH. However, TAL exhibited higher intrinsic efficacy than TRH in stimulating inositol-1,4,5-trisphosphate second messenger generation. This is the first study that elucidates the pharmacology of TAL at TRH-R and shows that TAL is a superagonist at TRH-R. We suggest the superagonism exhibited by TAL may in part explain its higher activity in mediating central nervous system effects in humans compared to TRH.
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spelling pubmed-34664662012-10-19 Taltirelin is a superagonist at the human thyrotropin-releasing hormone receptor Thirunarayanan, Nanthakumar Raaka, Bruce M. Gershengorn, Marvin C. Front Endocrinol (Lausanne) Endocrinology Taltirelin (TAL) is a thyrotropin-releasing hormone (TRH) analog that is approved for use in humans in Japan. In this study, we characterized TAL binding to and signaling by the human TRH receptor (TRH-R) in a model cell system. We found that TAL exhibited lower binding affinities than TRH and lower signaling potency via the inositol-1,4,5-trisphosphate/calcium pathway than TRH. However, TAL exhibited higher intrinsic efficacy than TRH in stimulating inositol-1,4,5-trisphosphate second messenger generation. This is the first study that elucidates the pharmacology of TAL at TRH-R and shows that TAL is a superagonist at TRH-R. We suggest the superagonism exhibited by TAL may in part explain its higher activity in mediating central nervous system effects in humans compared to TRH. Frontiers Media S.A. 2012-10-09 /pmc/articles/PMC3466466/ /pubmed/23087672 http://dx.doi.org/10.3389/fendo.2012.00120 Text en Copyright © Thirunarayanan, Raaka and Gershengorn. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Endocrinology
Thirunarayanan, Nanthakumar
Raaka, Bruce M.
Gershengorn, Marvin C.
Taltirelin is a superagonist at the human thyrotropin-releasing hormone receptor
title Taltirelin is a superagonist at the human thyrotropin-releasing hormone receptor
title_full Taltirelin is a superagonist at the human thyrotropin-releasing hormone receptor
title_fullStr Taltirelin is a superagonist at the human thyrotropin-releasing hormone receptor
title_full_unstemmed Taltirelin is a superagonist at the human thyrotropin-releasing hormone receptor
title_short Taltirelin is a superagonist at the human thyrotropin-releasing hormone receptor
title_sort taltirelin is a superagonist at the human thyrotropin-releasing hormone receptor
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3466466/
https://www.ncbi.nlm.nih.gov/pubmed/23087672
http://dx.doi.org/10.3389/fendo.2012.00120
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