Abstract |
We examined whether different itch signals converge on the same dorsal horn neurons in mice. Intradermal injections of histamine and SLIGRL-NH2 (protease-activated receptor-2 agonist) induced scratching in naive mice and so did mosquito allergen in sensitized mice. These stimuli induced Fos expression in cells in the superficial dorsal horn. Fos-positive cells were mainly distributed within the isolectin B4-labeled region (inner aspect of lamina II) after histamine injection. In contrast, they were in the region dorsal to the isolectin B4-labeled region after injections of SLIGRL-NH2 and mosquito allergen. These results suggest that allergic itch signal is mediated by primary afferents expressing protease-activated receptor-2 and the neurons receiving signals of protease-associated itch and allergy-associated itch are different from those of histamine-induced itch.
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Authors | Tasuku Nakano, Tsugunobu Andoh, Jung-Bum Lee, Yasushi Kuraishi |
Journal | Neuroreport
(Neuroreport)
Vol. 19
Issue 7
Pg. 723-6
(May 07 2008)
ISSN: 0959-4965 [Print] England |
PMID | 18418246
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Proto-Oncogene Proteins c-fos
- Receptor, PAR-2
- Histamine
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Topics |
- Afferent Pathways
(cytology, metabolism)
- Animals
- Histamine
(pharmacology)
- Hypersensitivity
(metabolism)
- Immunohistochemistry
- Mice
- Mice, Inbred ICR
- Posterior Horn Cells
(cytology, metabolism)
- Proto-Oncogene Proteins c-fos
(metabolism)
- Pruritus
(etiology, metabolism)
- Receptor, PAR-2
(metabolism)
- Skin
(innervation)
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