The kinin B1 receptor mediates alloknesis in a murine model of inflammation

•Non-noxious mechanical stimulus elicits itch in skin inflamed by complete Freund's adjuvant.•Subcutaneous naltrexone reduces alloknesis score.•Premedication with kinin B1 receptor antagonist reduces alloknesis score.•Premedication with kinin B2 receptor antagonist increases alloknesis score. N...

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Veröffentlicht in:Neuroscience letters 2014-02, Vol.560, p.31-35
Hauptverfasser: Feng, Jumian, Chen, Yuanzhen, Xiong, Jialing, Chen, Xu, Liang, Jiexian, Ji, Wenjin
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container_title Neuroscience letters
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creator Feng, Jumian
Chen, Yuanzhen
Xiong, Jialing
Chen, Xu
Liang, Jiexian
Ji, Wenjin
description •Non-noxious mechanical stimulus elicits itch in skin inflamed by complete Freund's adjuvant.•Subcutaneous naltrexone reduces alloknesis score.•Premedication with kinin B1 receptor antagonist reduces alloknesis score.•Premedication with kinin B2 receptor antagonist increases alloknesis score. Noxious stimuli and non-noxious mechanical stimuli elicit itch (alloknesis) instead of pain on skin lesions of patients with atopic dermatitis. We previously found that bradykinin evokes an itch-related scratching response through activation of kinin B1 receptor in skin inflamed using complete Freund's adjuvant. In this study we investigated whether alloknesis is evoked in CFA-inflamed skin and the involvement of kinin receptors. In our results, alloknesis was elicited four days after CFA-inflammation. Furthermore, pretreatment with a B1 receptor antagonist or μ-opioid receptor antagonist significantly reduced alloknesis. In contrast, treatment with a B2 receptor antagonist significantly increased alloknesis. These results suggest that the alloknesis response is mediated by the activation of kinin B1 receptor but antagonized by the B2 receptor in CFA-inflamed mice.
doi_str_mv 10.1016/j.neulet.2013.12.014
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Noxious stimuli and non-noxious mechanical stimuli elicit itch (alloknesis) instead of pain on skin lesions of patients with atopic dermatitis. We previously found that bradykinin evokes an itch-related scratching response through activation of kinin B1 receptor in skin inflamed using complete Freund's adjuvant. In this study we investigated whether alloknesis is evoked in CFA-inflamed skin and the involvement of kinin receptors. In our results, alloknesis was elicited four days after CFA-inflammation. Furthermore, pretreatment with a B1 receptor antagonist or μ-opioid receptor antagonist significantly reduced alloknesis. In contrast, treatment with a B2 receptor antagonist significantly increased alloknesis. 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Noxious stimuli and non-noxious mechanical stimuli elicit itch (alloknesis) instead of pain on skin lesions of patients with atopic dermatitis. We previously found that bradykinin evokes an itch-related scratching response through activation of kinin B1 receptor in skin inflamed using complete Freund's adjuvant. In this study we investigated whether alloknesis is evoked in CFA-inflamed skin and the involvement of kinin receptors. In our results, alloknesis was elicited four days after CFA-inflammation. Furthermore, pretreatment with a B1 receptor antagonist or μ-opioid receptor antagonist significantly reduced alloknesis. In contrast, treatment with a B2 receptor antagonist significantly increased alloknesis. These results suggest that the alloknesis response is mediated by the activation of kinin B1 receptor but antagonized by the B2 receptor in CFA-inflamed mice.</description><subject>Alloknesis</subject><subject>Animals</subject><subject>Bradykinin - pharmacology</subject><subject>Bradykinin B1 Receptor Antagonists</subject><subject>Bradykinin B2 Receptor Antagonists</subject><subject>Complete Freund's adjuvant</subject><subject>Dermatitis - etiology</subject><subject>Dermatitis - metabolism</subject><subject>Dermatitis - physiopathology</subject><subject>Freund's Adjuvant</subject><subject>Inflammation</subject><subject>Itch</subject><subject>Kinin B1 receptor</subject><subject>Male</subject><subject>Mice, Inbred C57BL</subject><subject>Physical Stimulation</subject><subject>Pruritus - etiology</subject><subject>Pruritus - metabolism</subject><subject>Pruritus - physiopathology</subject><subject>Receptor, Bradykinin B1 - metabolism</subject><subject>Receptor, Bradykinin B2 - metabolism</subject><subject>Receptors, Opioid, mu - antagonists &amp; 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inhibitors</topic><topic>Skin - metabolism</topic><topic>Touch</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feng, Jumian</creatorcontrib><creatorcontrib>Chen, Yuanzhen</creatorcontrib><creatorcontrib>Xiong, Jialing</creatorcontrib><creatorcontrib>Chen, Xu</creatorcontrib><creatorcontrib>Liang, Jiexian</creatorcontrib><creatorcontrib>Ji, Wenjin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Neuroscience letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feng, Jumian</au><au>Chen, Yuanzhen</au><au>Xiong, Jialing</au><au>Chen, Xu</au><au>Liang, Jiexian</au><au>Ji, Wenjin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The kinin B1 receptor mediates alloknesis in a murine model of inflammation</atitle><jtitle>Neuroscience letters</jtitle><addtitle>Neurosci Lett</addtitle><date>2014-02-07</date><risdate>2014</risdate><volume>560</volume><spage>31</spage><epage>35</epage><pages>31-35</pages><issn>0304-3940</issn><eissn>1872-7972</eissn><abstract>•Non-noxious mechanical stimulus elicits itch in skin inflamed by complete Freund's adjuvant.•Subcutaneous naltrexone reduces alloknesis score.•Premedication with kinin B1 receptor antagonist reduces alloknesis score.•Premedication with kinin B2 receptor antagonist increases alloknesis score. Noxious stimuli and non-noxious mechanical stimuli elicit itch (alloknesis) instead of pain on skin lesions of patients with atopic dermatitis. We previously found that bradykinin evokes an itch-related scratching response through activation of kinin B1 receptor in skin inflamed using complete Freund's adjuvant. In this study we investigated whether alloknesis is evoked in CFA-inflamed skin and the involvement of kinin receptors. In our results, alloknesis was elicited four days after CFA-inflammation. Furthermore, pretreatment with a B1 receptor antagonist or μ-opioid receptor antagonist significantly reduced alloknesis. In contrast, treatment with a B2 receptor antagonist significantly increased alloknesis. 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subjects Alloknesis
Animals
Bradykinin - pharmacology
Bradykinin B1 Receptor Antagonists
Bradykinin B2 Receptor Antagonists
Complete Freund's adjuvant
Dermatitis - etiology
Dermatitis - metabolism
Dermatitis - physiopathology
Freund's Adjuvant
Inflammation
Itch
Kinin B1 receptor
Male
Mice, Inbred C57BL
Physical Stimulation
Pruritus - etiology
Pruritus - metabolism
Pruritus - physiopathology
Receptor, Bradykinin B1 - metabolism
Receptor, Bradykinin B2 - metabolism
Receptors, Opioid, mu - antagonists & inhibitors
Skin - metabolism
Touch
title The kinin B1 receptor mediates alloknesis in a murine model of inflammation
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