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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9182086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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