Profiling of fatty acid metabolism in the dorsal root ganglion after peripheral nerve injury
Peripheral nerve injury (PNI) induces neuronal hyperexcitability, which underlies neuropathic pain. The emergence of RNA sequencing technologies has enabled profiling of transcriptional changes in pathological conditions. However, these approaches do not provide information regarding metabolites suc...
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Frontiers Media S.A.
2022-07-01
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Series: | Frontiers in Pain Research |
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Online Access: | https://www.frontiersin.org/articles/10.3389/fpain.2022.948689/full |
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author | Shota Yamamoto Tomomi Hashidate-Yoshida Takao Shimizu Takao Shimizu Hideo Shindou Hideo Shindou |
author_facet | Shota Yamamoto Tomomi Hashidate-Yoshida Takao Shimizu Takao Shimizu Hideo Shindou Hideo Shindou |
author_sort | Shota Yamamoto |
collection | DOAJ |
description | Peripheral nerve injury (PNI) induces neuronal hyperexcitability, which underlies neuropathic pain. The emergence of RNA sequencing technologies has enabled profiling of transcriptional changes in pathological conditions. However, these approaches do not provide information regarding metabolites such as lipids that are not directly encoded by genes. Fatty acids (FAs) are some of the essential lipids in mammalian organisms and are mainly stored as membrane phospholipids. In response to various biological stimuli, FAs are rapidly released and converted into several mediators, such as eicosanoids and docosanoids. FAs themselves or their metabolites play important roles in physiology and pathology. In this study, using a comprehensive lipidomic analysis of FA metabolites, 152 species were measured in the dorsal root ganglia of mice at multiple time points after PNI. We found that PNI increased the ω-6 FA metabolites produced by cyclooxygenases but not those produced by lipoxygenases or cytochrome P450 enzymes in the dorsal root ganglia. In contrast, ω-3 FA metabolites biosynthesized by any enzyme transiently increased after nerve injury. Overall, these findings provide a new resource and valuable insights into PNI pathologies, including pain and nerve regeneration. |
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issn | 2673-561X |
language | English |
last_indexed | 2024-04-14T07:29:08Z |
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spelling | doaj.art-576e878e97854bf58c925925e96aaf3c2022-12-22T02:05:55ZengFrontiers Media S.A.Frontiers in Pain Research2673-561X2022-07-01310.3389/fpain.2022.948689948689Profiling of fatty acid metabolism in the dorsal root ganglion after peripheral nerve injuryShota Yamamoto0Tomomi Hashidate-Yoshida1Takao Shimizu2Takao Shimizu3Hideo Shindou4Hideo Shindou5Department of Lipid Life Science, National Center for Global Health and Medicine, Tokyo, JapanDepartment of Lipid Life Science, National Center for Global Health and Medicine, Tokyo, JapanInstitute of Microbial Chemistry, Tokyo, JapanDepartment of Lipid Signaling, National Center for Global Health and Medicine, Tokyo, JapanDepartment of Lipid Life Science, National Center for Global Health and Medicine, Tokyo, JapanDepartment of Medical Lipid Science, Graduate School of Medicine, The University of Tokyo, Tokyo, JapanPeripheral nerve injury (PNI) induces neuronal hyperexcitability, which underlies neuropathic pain. The emergence of RNA sequencing technologies has enabled profiling of transcriptional changes in pathological conditions. However, these approaches do not provide information regarding metabolites such as lipids that are not directly encoded by genes. Fatty acids (FAs) are some of the essential lipids in mammalian organisms and are mainly stored as membrane phospholipids. In response to various biological stimuli, FAs are rapidly released and converted into several mediators, such as eicosanoids and docosanoids. FAs themselves or their metabolites play important roles in physiology and pathology. In this study, using a comprehensive lipidomic analysis of FA metabolites, 152 species were measured in the dorsal root ganglia of mice at multiple time points after PNI. We found that PNI increased the ω-6 FA metabolites produced by cyclooxygenases but not those produced by lipoxygenases or cytochrome P450 enzymes in the dorsal root ganglia. In contrast, ω-3 FA metabolites biosynthesized by any enzyme transiently increased after nerve injury. Overall, these findings provide a new resource and valuable insights into PNI pathologies, including pain and nerve regeneration.https://www.frontiersin.org/articles/10.3389/fpain.2022.948689/fulldorsal root ganglionfatty acidleukotrienlipid mediatorpainperipheral nerve injury |
spellingShingle | Shota Yamamoto Tomomi Hashidate-Yoshida Takao Shimizu Takao Shimizu Hideo Shindou Hideo Shindou Profiling of fatty acid metabolism in the dorsal root ganglion after peripheral nerve injury Frontiers in Pain Research dorsal root ganglion fatty acid leukotrien lipid mediator pain peripheral nerve injury |
title | Profiling of fatty acid metabolism in the dorsal root ganglion after peripheral nerve injury |
title_full | Profiling of fatty acid metabolism in the dorsal root ganglion after peripheral nerve injury |
title_fullStr | Profiling of fatty acid metabolism in the dorsal root ganglion after peripheral nerve injury |
title_full_unstemmed | Profiling of fatty acid metabolism in the dorsal root ganglion after peripheral nerve injury |
title_short | Profiling of fatty acid metabolism in the dorsal root ganglion after peripheral nerve injury |
title_sort | profiling of fatty acid metabolism in the dorsal root ganglion after peripheral nerve injury |
topic | dorsal root ganglion fatty acid leukotrien lipid mediator pain peripheral nerve injury |
url | https://www.frontiersin.org/articles/10.3389/fpain.2022.948689/full |
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