Multiple sweet receptors and transduction pathways revealed in knockout mice by temperature dependence and gurmarin sensitivity

被引:70
作者
Ohkuri, Tadahiro [1 ]
Yasumatsu, Keiko [1 ]
Horio, Nao [1 ]
Jyotaki, Masafumi [1 ]
Margolskee, Robert F. [2 ]
Ninomiya, Yuzo [1 ]
机构
[1] Kyushu Univ, Grad Sch Dent Sci, Sect Oral Neurosci, Higashi Ku, Fukuoka 8128582, Japan
[2] Mt Sinai Sch Med, Dept Neurosci, New York, NY USA
基金
日本学术振兴会;
关键词
sweet taste transduction; gurmarin sensitivity; temperature-dependent increase; knockout mice; chorda tympani nerve; CHORDA TYMPANI NERVE; TASTE BUD CELLS; CYCLIC-NUCLEOTIDES; INOSITOL 1,4,5-TRISPHOSPHATE; SIGNAL-TRANSDUCTION; NEURAL RESPONSES; BITTER TASTE; ACESULFAME-K; UMAMI TASTE; C57BL MICE;
D O I
10.1152/ajpregu.91018.2008
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Ohkuri T, Yasumatsu K, Horio N, Jyotaki M, Margolskee RF, Ninomiya Y. Multiple sweet receptors and transduction pathways revealed in knockout mice by temperature dependence and gurmarin sensitivity. Am J Physiol Regul Integr Comp Physiol 296: R960-R971, 2009. First published February 11, 2009; doi:10.1152/ajpregu.91018.2008.-Sweet taste transduction involves taste receptor type 1, member 2 (T1R2), taste receptor type 1, member 3 (T1R3), gustducin, and TRPM5. Because knockout (KO) mice lacking T1R3, gustducin's G alpha subunit (G alpha gust), or TRPM5 exhibited greatly reduced, but not abolished responses of the chorda tympani (CT) nerve to sweet compounds, it is likely that multiple sweet transduction pathways exist. That gurmarin (Gur), a sweet taste inhibitor, inhibits some but not all mouse CT responses to sweet compounds supports the existence of multiple sweet pathways. Here, we investigated Gur inhibition of CT responses to sweet compounds as a function of temperature in KO mice lacking T1R3, G alpha gust, or TRPM5. In T1R3-KO mice, responses to sucrose and glucose were Gur sensitive (GS) and displayed a temperature-dependent increase (TDI). In G alpha gust-KO mice, responses to sucrose and glucose were Gur-insensitive (GI) and showed a TDI. In TRPM5-KO mice, responses to glucose were GS and showed a TDI. All three KO mice exhibited no detectable responses to SC45647, and their responses to saccharin displayed neither GS nor a TDI. For all three KO mice, the lingual application of pronase, another sweet response inhibitor, almost fully abolished responses to sucrose and glucose but did not affect responses to saccharin. These results provide evidence for 1) the existence of multiple transduction pathways underlying responses to sugars: a T1R3-independent GS pathway for sucrose and glucose, and a TRPM5-independent temperature sensitive GS pathway for glucose; 2) the requirement for G alpha gust in GS sweet taste responses; and 3) the existence of a sweet independent pathway for saccharin, in mouse taste cells on the anterior tongue.
引用
收藏
页码:R960 / R971
页数:12
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