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Astaxanthin alleviates inflammatory pain by regulating the p38 mitogen-activated protein kinase and nuclear factor-erythroid factor 2-related factor/heme oxygenase-1 pathways in mice

Inflammatory pain is a complex process that has a substantial negative impact on post-injury quality of life. Astaxanthin (AST), which is a lipid-soluble red-orange carotenoid that is found in lobsters, inhibits the development and maintenance of inflammation in mice via its antioxidant and anti-inf...

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Published in:Food & function 2021-12, Vol.12 (24), p.12381-12394
Main Authors: Zhao, Lin, Tao, Xueshu, Wan, Chengfu, Dong, Daosong, Wang, Chenglong, Xi, Qi, Liu, Yan, Song, Tao
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cited_by cdi_FETCH-LOGICAL-c378t-e6f391b01b069da02f5575eef5aad8e3cf07886ec9dc71cd88169ddaac04eff93
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container_title Food & function
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creator Zhao, Lin
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Wan, Chengfu
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description Inflammatory pain is a complex process that has a substantial negative impact on post-injury quality of life. Astaxanthin (AST), which is a lipid-soluble red-orange carotenoid that is found in lobsters, inhibits the development and maintenance of inflammation in mice via its antioxidant and anti-inflammatory activities. However, the specific mechanisms underlying these effects remain unclear. In this study, we aimed to elucidate the mechanism by which astaxanthin alleviated inflammation using a mouse model with Complete Freund's adjuvant (CFA)-induced inflammatory pain. Mechanical allodynia and thermal hyperalgesia were observed on days 1-14 post CFA injection. Expression of p38 mitogen-activated protein kinase (MAPK) in the left paw and L4-6 dorsal root ganglia (DRG) were upregulated in the CFA-induced mice. Expression of the nuclear factor erythroid 2-related factor 2 (Nrf2)/heme oxygenase-1 (HO-1) pathways were also increased. Astaxanthin relieved mechanical allodynia and thermal hyperalgesia induced by CFA and inhibited the inflammatory response ( e.g. , infiltration of inflammatory cells and production of inflammatory factors) in the ipsilateral paw and DRG. Additionally, AST inhibited p38 MAPK and enhanced Nrf2/HO-1 contents in the left paw and DRG, and reversed the pain induced by p38 MAPK agonist and Nrf2 inhibitors. These findings suggest that AST exerts anti-inflammatory effects and regulates p38 MAPK and Nrf2/HO-1 to alleviate inflammatory pain. AST may be a potential therapeutic agent for relieving inflammation. Astaxanthin suppressed the CFA-induced upregulation of p38 MAPK and enhanced Nrf2/HO-1 pathway. Additionally, AST reduced the inflammatory response ( e.g. , inflammatory cells and pro-inflammatory factors) to alleviate symptoms of inflammatory pain.
doi_str_mv 10.1039/d1fo02326h
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Astaxanthin (AST), which is a lipid-soluble red-orange carotenoid that is found in lobsters, inhibits the development and maintenance of inflammation in mice via its antioxidant and anti-inflammatory activities. However, the specific mechanisms underlying these effects remain unclear. In this study, we aimed to elucidate the mechanism by which astaxanthin alleviated inflammation using a mouse model with Complete Freund's adjuvant (CFA)-induced inflammatory pain. Mechanical allodynia and thermal hyperalgesia were observed on days 1-14 post CFA injection. Expression of p38 mitogen-activated protein kinase (MAPK) in the left paw and L4-6 dorsal root ganglia (DRG) were upregulated in the CFA-induced mice. Expression of the nuclear factor erythroid 2-related factor 2 (Nrf2)/heme oxygenase-1 (HO-1) pathways were also increased. Astaxanthin relieved mechanical allodynia and thermal hyperalgesia induced by CFA and inhibited the inflammatory response ( e.g. , infiltration of inflammatory cells and production of inflammatory factors) in the ipsilateral paw and DRG. Additionally, AST inhibited p38 MAPK and enhanced Nrf2/HO-1 contents in the left paw and DRG, and reversed the pain induced by p38 MAPK agonist and Nrf2 inhibitors. These findings suggest that AST exerts anti-inflammatory effects and regulates p38 MAPK and Nrf2/HO-1 to alleviate inflammatory pain. AST may be a potential therapeutic agent for relieving inflammation. Astaxanthin suppressed the CFA-induced upregulation of p38 MAPK and enhanced Nrf2/HO-1 pathway. 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Astaxanthin relieved mechanical allodynia and thermal hyperalgesia induced by CFA and inhibited the inflammatory response ( e.g. , infiltration of inflammatory cells and production of inflammatory factors) in the ipsilateral paw and DRG. Additionally, AST inhibited p38 MAPK and enhanced Nrf2/HO-1 contents in the left paw and DRG, and reversed the pain induced by p38 MAPK agonist and Nrf2 inhibitors. These findings suggest that AST exerts anti-inflammatory effects and regulates p38 MAPK and Nrf2/HO-1 to alleviate inflammatory pain. AST may be a potential therapeutic agent for relieving inflammation. Astaxanthin suppressed the CFA-induced upregulation of p38 MAPK and enhanced Nrf2/HO-1 pathway. Additionally, AST reduced the inflammatory response ( e.g. , inflammatory cells and pro-inflammatory factors) to alleviate symptoms of inflammatory pain.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>34825683</pmid><doi>10.1039/d1fo02326h</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-3999-4535</orcidid></addata></record>
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source Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list)
subjects Animals
Anti-Inflammatory Agents - pharmacology
Anti-Inflammatory Agents - therapeutic use
Antioxidants
Astaxanthin
Chemical compounds
Disease Models, Animal
Dorsal root ganglia
Freund's adjuvant
Ganglia
Heme
Heme oxygenase (decyclizing)
Heme Oxygenase-1 - metabolism
Inflammation
Inflammation - drug therapy
Inflammatory response
Kinases
Lipids
Lobsters
Male
MAP kinase
Membrane Proteins - metabolism
Mice
Mice, Inbred C57BL
NF-E2-Related Factor 2 - metabolism
Oxygenase
p38 Mitogen-Activated Protein Kinases - metabolism
Pain
Pain Measurement - drug effects
Pain perception
Pharmacology
Phytotherapy
Protein kinase
Proteins
Quality of life
Xanthophylls - pharmacology
Xanthophylls - therapeutic use
title Astaxanthin alleviates inflammatory pain by regulating the p38 mitogen-activated protein kinase and nuclear factor-erythroid factor 2-related factor/heme oxygenase-1 pathways in mice
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