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Galantamine attenuates autoinflammation in a mouse model of familial mediterranean fever

BACKGROUND: Autoinflammatory diseases, a diverse group of inherited conditions characterized by excessive innate immune activation, have limited therapeutic options. Neuroimmune circuits of the inflammatory reflex control innate immune overactivation and can be stimulated to treat disease using the...

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Autores principales: Mughrabi, Ibrahim T., Ochani, Mahendar, Tanovic, Mirza, Wang, Ping, Diamond, Betty, Sherry, Barbara, Pavlov, Valentin A., Ozen, Seza, Kastner, Daniel L., Chae, Jae Jin, Al-Abed, Yousef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733251/
https://www.ncbi.nlm.nih.gov/pubmed/36494621
http://dx.doi.org/10.1186/s10020-022-00571-9
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author Mughrabi, Ibrahim T.
Ochani, Mahendar
Tanovic, Mirza
Wang, Ping
Diamond, Betty
Sherry, Barbara
Pavlov, Valentin A.
Ozen, Seza
Kastner, Daniel L.
Chae, Jae Jin
Al-Abed, Yousef
author_facet Mughrabi, Ibrahim T.
Ochani, Mahendar
Tanovic, Mirza
Wang, Ping
Diamond, Betty
Sherry, Barbara
Pavlov, Valentin A.
Ozen, Seza
Kastner, Daniel L.
Chae, Jae Jin
Al-Abed, Yousef
author_sort Mughrabi, Ibrahim T.
collection PubMed
description BACKGROUND: Autoinflammatory diseases, a diverse group of inherited conditions characterized by excessive innate immune activation, have limited therapeutic options. Neuroimmune circuits of the inflammatory reflex control innate immune overactivation and can be stimulated to treat disease using the acetylcholinesterase inhibitor galantamine. METHODS: We tested the efficacy of galantamine in a rodent model of the prototypical autoinflammatory disease familial Mediterranean fever (FMF). Multiple chronic disease markers were evaluated in animals that received long-term galantamine treatment compared to vehicle. RESULTS: Long-term treatment with galantamine attenuated the associated splenomegaly and anemia which are characteristic features of this disease. Further, treatment reduced inflammatory cell infiltration into affected organs and a subcutaneous air pouch. CONCLUSIONS: These findings suggest that galantamine attenuates chronic inflammation in this mouse model of FMF. Further research is warranted to explore the therapeutic potential of galantamine in FMF and other autoinflammatory diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s10020-022-00571-9.
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spelling pubmed-97332512022-12-10 Galantamine attenuates autoinflammation in a mouse model of familial mediterranean fever Mughrabi, Ibrahim T. Ochani, Mahendar Tanovic, Mirza Wang, Ping Diamond, Betty Sherry, Barbara Pavlov, Valentin A. Ozen, Seza Kastner, Daniel L. Chae, Jae Jin Al-Abed, Yousef Mol Med Short Report BACKGROUND: Autoinflammatory diseases, a diverse group of inherited conditions characterized by excessive innate immune activation, have limited therapeutic options. Neuroimmune circuits of the inflammatory reflex control innate immune overactivation and can be stimulated to treat disease using the acetylcholinesterase inhibitor galantamine. METHODS: We tested the efficacy of galantamine in a rodent model of the prototypical autoinflammatory disease familial Mediterranean fever (FMF). Multiple chronic disease markers were evaluated in animals that received long-term galantamine treatment compared to vehicle. RESULTS: Long-term treatment with galantamine attenuated the associated splenomegaly and anemia which are characteristic features of this disease. Further, treatment reduced inflammatory cell infiltration into affected organs and a subcutaneous air pouch. CONCLUSIONS: These findings suggest that galantamine attenuates chronic inflammation in this mouse model of FMF. Further research is warranted to explore the therapeutic potential of galantamine in FMF and other autoinflammatory diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s10020-022-00571-9. BioMed Central 2022-12-09 /pmc/articles/PMC9733251/ /pubmed/36494621 http://dx.doi.org/10.1186/s10020-022-00571-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Short Report
Mughrabi, Ibrahim T.
Ochani, Mahendar
Tanovic, Mirza
Wang, Ping
Diamond, Betty
Sherry, Barbara
Pavlov, Valentin A.
Ozen, Seza
Kastner, Daniel L.
Chae, Jae Jin
Al-Abed, Yousef
Galantamine attenuates autoinflammation in a mouse model of familial mediterranean fever
title Galantamine attenuates autoinflammation in a mouse model of familial mediterranean fever
title_full Galantamine attenuates autoinflammation in a mouse model of familial mediterranean fever
title_fullStr Galantamine attenuates autoinflammation in a mouse model of familial mediterranean fever
title_full_unstemmed Galantamine attenuates autoinflammation in a mouse model of familial mediterranean fever
title_short Galantamine attenuates autoinflammation in a mouse model of familial mediterranean fever
title_sort galantamine attenuates autoinflammation in a mouse model of familial mediterranean fever
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733251/
https://www.ncbi.nlm.nih.gov/pubmed/36494621
http://dx.doi.org/10.1186/s10020-022-00571-9
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