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Resolvin E1 Attenuates Chronic Pain-Induced Depression-Like Behavior in Mice: Possible Involvement of Chemerin Receptor ChemR23

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Title: Resolvin E1 Attenuates Chronic Pain-Induced Depression-Like Behavior in Mice: Possible Involvement of Chemerin Receptor ChemR23
Authors: Suzuki, Hiroe Browse this author
Otsuka, Takahisa Browse this author
Hitora-Imamura, Natsuko Browse this author
Ishimura, Kohei Browse this author
Fukuda, Hayato Browse this author
Fujiwara, Koichi Browse this author →KAKEN DB
Shuto, Satoshi Browse this author →KAKEN DB
Deyama, Satoshi Browse this author →KAKEN DB
Minami, Masabumi Browse this author →KAKEN DB
Keywords: resolvin
n-3 polyunsaturated fatty acid
antidepressant
pain
Issue Date: 1-Oct-2021
Publisher: The Pharmaceutical Society of Japan (日本薬学会)
Journal Title: Biological & pharmaceutical bulletin
Volume: 44
Issue: 10
Start Page: 1548
End Page: 1550
Publisher DOI: 10.1248/bpb.b21-00461
Abstract: The antidepressant effect of eicosapentaenoic acid-derived bioactive lipid, resolvin E1 (RvE1), was examined in a murine model of chronic pain-induced depression using a tail suspension test. Because RvE1 reportedly possesses agonistic activity on a chemerin receptor ChemR23, we also examined the antidepressant effect of chemerin. Two weeks after surgery for unilateral spared nerve injury to prepare neuropathic pain model mice, immobility time was measured in a tail suspension test. Chronic pain significantly increased immobility time, and this depression-like behavior was attenuated by intracerebroventricular injection of RvE1 (1 ng) or chemerin (500 ng). These results demonstrate that RvE1 exerts an antidepressant effect in a murine model of chronic pain-induced depression, which is likely to be via ChemR23. RvE1 and its receptor may be promising targets to develop novel antidepressants.
Type: article
URI: http://hdl.handle.net/2115/83324
Appears in Collections:薬学研究院 (Faculty of Pharmaceutical Sciences) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

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