Bitter taste receptor T2R1 activities were compatible with behavioral sensitivity to bitterness in chickens

Clarification of the mechanism of the sense of taste in chickens will provide information useful for creating and improving new feedstuffs for chickens, because the character of the taste receptors in oral tissues affects feeding behavior in animals. In this study, we focused on the sensitivity to b...

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Veröffentlicht in:Biochemical and biophysical research communications 2015-05, Vol.460 (2), p.464-468
Hauptverfasser: Hirose, Nozomi, Kawabata, Yuko, Kawabata, Fuminori, Nishimura, Shotaro, Tabata, Shoji
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Sprache:eng
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Zusammenfassung:Clarification of the mechanism of the sense of taste in chickens will provide information useful for creating and improving new feedstuffs for chickens, because the character of the taste receptors in oral tissues affects feeding behavior in animals. In this study, we focused on the sensitivity to bitterness in chickens. We cloned one of the bitter taste receptors, T2R1, from the chicken palate, constructed several biosensor-cells expressing chicken T2R1 (cT2R1), and determined a highly sensitive biosensor of cT2R1 among them. By using Ca2+ imaging methods, we identified two agonists of cT2R1, dextromethorphan (Dex) and diphenidol (Dip). Dex was a new agonist of cT2R1 that was more potent than Dip. In a behavioral drinking study, the intake volumes of solutions of these compounds were significantly lower than that of water in chickens. These aversive concentrations were identical to the concentrations that could activate cT2R1 in a cell-based assay. These results suggest that the cT2R1 activities induced by these agonists are linked to behavioral sensitivity to bitterness in chickens. •We cloned the chicken bitter taste receptor gene, cT2R1, from the chicken palate.•We constructed a highly sensitive biosensor of cT2R1.•We identified two agonists of cT2R1, dextromethorphan and diphenidol.•cT2R1 activities were linked to behavioral sensitivity to bitterness in chickens.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2015.03.056