Intrathecal administration of low-dose nociceptin/orphanin FQ induces allodynia via c-Jun N-terminal kinase and monocyte chemoattractant protein-1.

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Intrathecal administration of low-dose nociceptin/orphanin FQ induces allodynia via c-Jun N-terminal kinase and monocyte chemoattractant protein-1.

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

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name

Intrathecal administration of ...... yte chemoattractant protein-1.

@en

Intrathecal administration of ...... yte chemoattractant protein-1.

@nl

type

Item

label

Intrathecal administration of ...... yte chemoattractant protein-1.

@en

Intrathecal administration of ...... yte chemoattractant protein-1.

@nl

prefLabel

Intrathecal administration of ...... yte chemoattractant protein-1.

@en

Intrathecal administration of ...... yte chemoattractant protein-1.

@nl

P1476

Intrathecal administration of ...... yte chemoattractant protein-1.

@en

P2093

Emiko Okuda-Ashitaka

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Isamu Nishimura

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Kenta Kawabata

http://www.w3.org/2001/XMLSchema#string

Shoko Terauchi

http://www.w3.org/2001/XMLSchema#string

Takeshi Fujiwara

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Toshiaki Minami

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P2860

Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor

The ORL1 receptor: molecular pharmacology and signalling mechanisms

The nociceptin/orphanin FQ receptor: a target with broad therapeutic potential

Characterization of nociceptin/orphanin FQ-induced pain responses in conscious mice: neonatal capsaicin treatment and N-methyl-D-aspartate receptor GluRepsilon subunit knockout mice

Ethical guidelines for investigations of experimental pain in conscious animals

MAP kinase and pain.

Role of JNK isoforms in the development of neuropathic pain following sciatic nerve transection in the mouse.

Nociceptin/orphanin FQ-induced nociceptive responses through substance P release from peripheral nerve endings in mice.

Novel helix-constrained nociceptin derivatives are potent agonists and antagonists of ERK phosphorylation and thermal analgesia in mice.

Characterization of nociceptin/orphanin FQ-induced pain responses by the novel receptor antagonist N-(4-amino-2-methylquinolin-6-yl)-2-(4-ethylphenoxymethyl) benzamide monohydrochloride.

P304

1499-1508

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P31

scholarly article

P356

10.1111/EJN.13247

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P407

English

P433

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P478

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Seiji Ito

P577

2016-04-02T00:00:00Z

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P698

27038234

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P921

nociceptin