ID | 62435 |
フルテキストURL | |
著者 |
Matsumoto, Ryohtaroh
Division of Biochemistry, Graduate School of Pharmaceutical Science and Faculty of Pharmacy, Keio University
Takahashi, Daisuke
Division of Biochemistry, Graduate School of Pharmaceutical Science and Faculty of Pharmacy, Keio University
Watanabe, Masaki
Division of Pharmaceutical Sciences, Graduate School of Medicine Dentistry and Pharmaceutical Sciences, Okayama University
Nakatani, Shunsuke
Division of Pharmaceutical Sciences, Graduate School of Medicine Dentistry and Pharmaceutical Sciences, Okayama University
Takamura, Yuta
Division of Pharmaceutical Sciences, Graduate School of Medicine Dentistry and Pharmaceutical Sciences, Okayama University
Kurosaki, Yuji
Division of Pharmaceutical Sciences, Graduate School of Medicine Dentistry and Pharmaceutical Sciences, Okayama University
Kaken ID
publons
researchmap
Kakuta, Hiroki
Division of Pharmaceutical Sciences, Graduate School of Medicine Dentistry and Pharmaceutical Sciences, Okayama University
ORCID
Kaken ID
publons
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Hase, Koji
Division of Biochemistry, Graduate School of Pharmaceutical Science and Faculty of Pharmacy, Keio University
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抄録 | Retinoid X receptor (RXR) is a nuclear receptor that heterodimerizes with several nuclear receptors, integrating ligand-mediated signals across the heterodimers. Synthetic RXR agonists have been developed to cure certain inflammatory diseases, including inflammatory bowel diseases (IBDs). However, pre-existing RXR agonists, which are lipophilic and readily absorbed in the upper intestine, cause considerable adverse effects such as hepatomegaly, hyperlipidemia, and hypothyroidism. To minimize these adverse effects, we have developed an RXR agonist, NEt-3IB, which has lipophilic and thus poorly absorptive properties. In this study, we evaluated the effects of NEt-3IB in an experimental murine colitis model induced through the adoptive transfer of CD45RB(high)CD4(+) T cells. Pharmacokinetic studies demonstrated that the major portion of NEt-3IB was successfully delivered to the large intestine after oral administration. Notably, NEt-3IB treatment suppressed the development of T cell-mediated chronic colitis, as indicated by improvement of wasting symptoms, inflammatory infiltration, and mucosal hyperplasia. The protective effect of NEt-3IB was mediated by the suppression of IFN-gamma-producing Th1 cell expansion in the colon. In conclusion, NEt-3IB, a large intestine-directed RXR agonist, is a promising drug candidate for IBDs.
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キーワード | RXR
NEt-3IB
inflammatory bowel disease
colitis
Th1 cells
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発行日 | 2021-08-12
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出版物タイトル |
Frontiers In Pharmacology
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巻 | 12巻
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出版者 | Frontiers Media SA
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開始ページ | 715752
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ISSN | 1663-9812
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資料タイプ |
学術雑誌論文
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言語 |
英語
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OAI-PMH Set |
岡山大学
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著作権者 | © 2021 Matsumoto, Takahashi, Watanabe, Nakatani, Takamura,Kurosaki, Kakuta and Hase.
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論文のバージョン | publisher
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PubMed ID | |
DOI | |
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関連URL | isVersionOf https://doi.org/10.3389/fphar.2021.715752
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ライセンス | https://creativecommons.org/licenses/by/4.0/
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助成番号 | Matsumoto R, Takahashi D, Watanabe M, Nakatani S, Takamura Y, Kurosaki Y, Kakuta H and Hase K (2021) A Retinoid X Receptor Agonist Directed to the Large Intestine Ameliorates T-Cell-Mediated Colitis in Mice. Front. Pharmacol. 12:715752. doi: 10.3389/fphar.2021.715752
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オープンアクセス(出版社) |
OA
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