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Identification of New Non-BBB Permeable Tryptophan Hydroxylase Inhibitors for Treating Obesity and Fatty Liver Disease

Serotonin (5-hydroxytryptophan) is a hormone that regulates emotions in the central nervous system. However, serotonin in the peripheral system is associated with obesity and fatty liver disease. Because serotonin cannot cross the blood-brain barrier (BBB), we focused on identifying new tryptophan h...

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Autores principales: Pagire, Suvarna H., Pagire, Haushabhau S., Park, Kun-Young, Bae, Eun Jung, Kim, Kwang-eun, Kim, Minhee, Yoon, Jihyeon, Parameswaran, Saravanan, Choi, Jun-Ho, Park, Sungmi, Jeon, Jae-Han, Song, Jin Sook, Bae, Myung Ae, Lee, In-Kyu, Kim, Hail, Suh, Jae Myoung, Ahn, Jin Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182086/
https://www.ncbi.nlm.nih.gov/pubmed/35684355
http://dx.doi.org/10.3390/molecules27113417
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author Pagire, Suvarna H.
Pagire, Haushabhau S.
Park, Kun-Young
Bae, Eun Jung
Kim, Kwang-eun
Kim, Minhee
Yoon, Jihyeon
Parameswaran, Saravanan
Choi, Jun-Ho
Park, Sungmi
Jeon, Jae-Han
Song, Jin Sook
Bae, Myung Ae
Lee, In-Kyu
Kim, Hail
Suh, Jae Myoung
Ahn, Jin Hee
author_facet Pagire, Suvarna H.
Pagire, Haushabhau S.
Park, Kun-Young
Bae, Eun Jung
Kim, Kwang-eun
Kim, Minhee
Yoon, Jihyeon
Parameswaran, Saravanan
Choi, Jun-Ho
Park, Sungmi
Jeon, Jae-Han
Song, Jin Sook
Bae, Myung Ae
Lee, In-Kyu
Kim, Hail
Suh, Jae Myoung
Ahn, Jin Hee
author_sort Pagire, Suvarna H.
collection PubMed
description Serotonin (5-hydroxytryptophan) is a hormone that regulates emotions in the central nervous system. However, serotonin in the peripheral system is associated with obesity and fatty liver disease. Because serotonin cannot cross the blood-brain barrier (BBB), we focused on identifying new tryptophan hydroxylase type I (TPH1) inhibitors that act only in peripheral tissues for treating obesity and fatty liver disease without affecting the central nervous system. Structural optimization inspired by para-chlorophenylalanine (pCPA) resulted in the identification of a series of oxyphenylalanine and heterocyclic phenylalanine derivatives as TPH1 inhibitors. Among these compounds, compound 18i with an IC(50) value of 37 nM was the most active in vitro. Additionally, compound 18i showed good liver microsomal stability and did not significantly inhibit CYP and Herg. Furthermore, this TPH1 inhibitor was able to actively interact with the peripheral system without penetrating the BBB. Compound 18i and its prodrug reduced body weight gain in mammals and decreased in vivo fat accumulation.
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spelling pubmed-91820862022-06-10 Identification of New Non-BBB Permeable Tryptophan Hydroxylase Inhibitors for Treating Obesity and Fatty Liver Disease Pagire, Suvarna H. Pagire, Haushabhau S. Park, Kun-Young Bae, Eun Jung Kim, Kwang-eun Kim, Minhee Yoon, Jihyeon Parameswaran, Saravanan Choi, Jun-Ho Park, Sungmi Jeon, Jae-Han Song, Jin Sook Bae, Myung Ae Lee, In-Kyu Kim, Hail Suh, Jae Myoung Ahn, Jin Hee Molecules Article Serotonin (5-hydroxytryptophan) is a hormone that regulates emotions in the central nervous system. However, serotonin in the peripheral system is associated with obesity and fatty liver disease. Because serotonin cannot cross the blood-brain barrier (BBB), we focused on identifying new tryptophan hydroxylase type I (TPH1) inhibitors that act only in peripheral tissues for treating obesity and fatty liver disease without affecting the central nervous system. Structural optimization inspired by para-chlorophenylalanine (pCPA) resulted in the identification of a series of oxyphenylalanine and heterocyclic phenylalanine derivatives as TPH1 inhibitors. Among these compounds, compound 18i with an IC(50) value of 37 nM was the most active in vitro. Additionally, compound 18i showed good liver microsomal stability and did not significantly inhibit CYP and Herg. Furthermore, this TPH1 inhibitor was able to actively interact with the peripheral system without penetrating the BBB. Compound 18i and its prodrug reduced body weight gain in mammals and decreased in vivo fat accumulation. MDPI 2022-05-25 /pmc/articles/PMC9182086/ /pubmed/35684355 http://dx.doi.org/10.3390/molecules27113417 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
Pagire, Suvarna H.
Pagire, Haushabhau S.
Park, Kun-Young
Bae, Eun Jung
Kim, Kwang-eun
Kim, Minhee
Yoon, Jihyeon
Parameswaran, Saravanan
Choi, Jun-Ho
Park, Sungmi
Jeon, Jae-Han
Song, Jin Sook
Bae, Myung Ae
Lee, In-Kyu
Kim, Hail
Suh, Jae Myoung
Ahn, Jin Hee
Identification of New Non-BBB Permeable Tryptophan Hydroxylase Inhibitors for Treating Obesity and Fatty Liver Disease
title Identification of New Non-BBB Permeable Tryptophan Hydroxylase Inhibitors for Treating Obesity and Fatty Liver Disease
title_full Identification of New Non-BBB Permeable Tryptophan Hydroxylase Inhibitors for Treating Obesity and Fatty Liver Disease
title_fullStr Identification of New Non-BBB Permeable Tryptophan Hydroxylase Inhibitors for Treating Obesity and Fatty Liver Disease
title_full_unstemmed Identification of New Non-BBB Permeable Tryptophan Hydroxylase Inhibitors for Treating Obesity and Fatty Liver Disease
title_short Identification of New Non-BBB Permeable Tryptophan Hydroxylase Inhibitors for Treating Obesity and Fatty Liver Disease
title_sort identification of new non-bbb permeable tryptophan hydroxylase inhibitors for treating obesity and fatty liver disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182086/
https://www.ncbi.nlm.nih.gov/pubmed/35684355
http://dx.doi.org/10.3390/molecules27113417
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