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Changes in median eminence of fatty acid–binding protein 3 in a mouse model of pain
AIMS: Fatty acid–binding protein (FABP) regulates polyunsaturated fatty acid (PUFA) intracellular trafficking and signal transduction. Our previous studies demonstrated that the alteration of PUFA in the hypothalamus is involved in pain process. However, how FABP subtypes change during pain remain u...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919114/ https://www.ncbi.nlm.nih.gov/pubmed/35090101 http://dx.doi.org/10.1002/npr2.12225 |
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author | Tachibana, Dan Nakamoto, Kazuo Tokuyama, Shogo |
author_facet | Tachibana, Dan Nakamoto, Kazuo Tokuyama, Shogo |
author_sort | Tachibana, Dan |
collection | PubMed |
description | AIMS: Fatty acid–binding protein (FABP) regulates polyunsaturated fatty acid (PUFA) intracellular trafficking and signal transduction. Our previous studies demonstrated that the alteration of PUFA in the hypothalamus is involved in pain process. However, how FABP subtypes change during pain remain unclear. Here, we examined the expression changes and localization in the hypothalamic FABP subtype in postoperative pain model mice. METHODS: Paw incision–induced postoperative methods were adopted as a pain model in male ddY mice. Mechanical allodynia was examined using the von Frey test. The analysis of several FABPs mRNA was measured by real‐time PCR, and cellular localization of its protein level was measured by immunofluorescent study. RESULTS: Postoperative pain mouse elicited mechanical allodynia on Day 2 after paw incision, and mRNA expression of FABP3 increased significantly in the hypothalamus in the postoperative pain mouse model compared to that in control mice. FABP3 protein expressed in the median eminence and the arcuate nucleus, and colocalized with Iba‐1, which is a microglial cell marker. Its protein level significantly increased in the median eminence on Day 2 after incision and returned to the control level on Day 4 after incision. CONCLUSIONS: Our findings indicate that FABP3 in the median eminence may change in pain stimuli and may represent a molecular link controlling pain. |
format | Online Article Text |
id | pubmed-8919114 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89191142022-03-18 Changes in median eminence of fatty acid–binding protein 3 in a mouse model of pain Tachibana, Dan Nakamoto, Kazuo Tokuyama, Shogo Neuropsychopharmacol Rep Original Articles AIMS: Fatty acid–binding protein (FABP) regulates polyunsaturated fatty acid (PUFA) intracellular trafficking and signal transduction. Our previous studies demonstrated that the alteration of PUFA in the hypothalamus is involved in pain process. However, how FABP subtypes change during pain remain unclear. Here, we examined the expression changes and localization in the hypothalamic FABP subtype in postoperative pain model mice. METHODS: Paw incision–induced postoperative methods were adopted as a pain model in male ddY mice. Mechanical allodynia was examined using the von Frey test. The analysis of several FABPs mRNA was measured by real‐time PCR, and cellular localization of its protein level was measured by immunofluorescent study. RESULTS: Postoperative pain mouse elicited mechanical allodynia on Day 2 after paw incision, and mRNA expression of FABP3 increased significantly in the hypothalamus in the postoperative pain mouse model compared to that in control mice. FABP3 protein expressed in the median eminence and the arcuate nucleus, and colocalized with Iba‐1, which is a microglial cell marker. Its protein level significantly increased in the median eminence on Day 2 after incision and returned to the control level on Day 4 after incision. CONCLUSIONS: Our findings indicate that FABP3 in the median eminence may change in pain stimuli and may represent a molecular link controlling pain. John Wiley and Sons Inc. 2022-01-28 /pmc/articles/PMC8919114/ /pubmed/35090101 http://dx.doi.org/10.1002/npr2.12225 Text en © 2022 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Neuropsychopharmacology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Tachibana, Dan Nakamoto, Kazuo Tokuyama, Shogo Changes in median eminence of fatty acid–binding protein 3 in a mouse model of pain |
title | Changes in median eminence of fatty acid–binding protein 3 in a mouse model of pain |
title_full | Changes in median eminence of fatty acid–binding protein 3 in a mouse model of pain |
title_fullStr | Changes in median eminence of fatty acid–binding protein 3 in a mouse model of pain |
title_full_unstemmed | Changes in median eminence of fatty acid–binding protein 3 in a mouse model of pain |
title_short | Changes in median eminence of fatty acid–binding protein 3 in a mouse model of pain |
title_sort | changes in median eminence of fatty acid–binding protein 3 in a mouse model of pain |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919114/ https://www.ncbi.nlm.nih.gov/pubmed/35090101 http://dx.doi.org/10.1002/npr2.12225 |
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