α7 nicotinic acetylcholine receptor agonist attenuates allergen-induced immediate nasal response in murine model of allergic rhinitis

The expression of nicotinic acetylcholine receptor (nAChR) subunits on various immune cells suggests their involvement in allergic rhinitis. However, how exactly they contribute to this pathogenesis is not yet confirmed. Our present study examined the therapeutic potential of GTS-21, an α7 nAChR ago...

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Published inJournal of Veterinary Medical Science Vol. 86; no. 7; pp. 824 - 827
Main Authors OGATA, Sawako, MIURA, Kento, MATSUURA, Anna, HOSOMI, Naohisa, MORI, Akio, YAMASHITA, Shuhei, YAMASAKI, Norimasa, KITAMURA, Noriko, UDA, Naoto, GOTOH, Minoru, NAKAJIMA, Shotaro, KAMINUMA, Osamu
Format Journal Article
LanguageEnglish
Published Japan JAPANESE SOCIETY OF VETERINARY SCIENCE 2024
Japan Science and Technology Agency
The Japanese Society of Veterinary Science
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ISSN0916-7250
1347-7439
1347-7439
DOI10.1292/jvms.24-0033

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Summary:The expression of nicotinic acetylcholine receptor (nAChR) subunits on various immune cells suggests their involvement in allergic rhinitis. However, how exactly they contribute to this pathogenesis is not yet confirmed. Our present study examined the therapeutic potential of GTS-21, an α7 nAChR agonist, for treating allergic rhinitis by employing its mouse models. GTS-21 treatment reduced allergen-induced immediate nasal response in ovalbumin (OVA)-sensitized model. However, nasal hyperresponsiveness or eosinophil infiltration elicited in either the OVA-sensitized or T helper 2 cell-transplanted model was not affected by GTS-21. GTS-21 did not alter allergen-induced passive cutaneous anaphylaxis response in anti-dinitrophenyl IgE-sensitized mice. This evidence implies GTS-21’s potential to alleviate allergic rhinitis without perturbing T cells or mast cells.
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These authors contributed equally to this work.
ISSN:0916-7250
1347-7439
1347-7439
DOI:10.1292/jvms.24-0033