首页> 美国卫生研究院文献>The Journal of Physiology >Involvement of multiple taste receptors in umami taste: analysis of gustatory nerve responses in metabotropic glutamate receptor 4 knockout mice
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Involvement of multiple taste receptors in umami taste: analysis of gustatory nerve responses in metabotropic glutamate receptor 4 knockout mice

机译:多种味觉受体参与鲜味:代谢型谷氨酸受体4基因敲除小鼠味觉神经反应的分析

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摘要

Umami taste is elicited by l-glutamate and some other amino acids and is thought to be initiated by G-protein-coupled receptors. Proposed umami receptors include heterodimers of taste receptor type 1, members 1 and 3 (T1R1 + T1R3), and metabotropic glutamate receptors 1 and 4 (mGluR1 and mGluR4). Accumulated evidences support the involvement of T1R1 + T1R3 in umami responses in mice. However, little is known about the in vivo function of mGluR in umami taste. Here, we examined taste responses of the chorda tympani (CT) and the glossopharyngeal (GL) nerves in wild-type mice and mice genetically lacking mGluR4 (mGluR4-KO). Our results indicated that compared to wild-type mice, mGluR4-KO mice showed significantly smaller gustatory nerve responses to glutamate and l-(+)-2-amino-4-phosphonobutyrate (an agonist for group III mGluR) in both the CT and GL nerves without affecting responses to other taste stimuli. Residual glutamate responses in mGluR4-KO mice were not affected by (RS)-alpha-cyclopropyl-4-phosphonophenylglycine (an antagonist for group III mGluR), but were suppressed by gurmarin (a T1R3 blocker) in the CT and (RS)-1-aminoindan-1,5-dicarboxylic acid (an antagonist for group I mGluR) in the CT and GL nerve. In wild-type mice, both quisqualic acid (an agonist for group I mGluR) and l-(+)-2-amino-4-phosphonobutyrate elicited gustatory nerve responses and these responses were suppressed by addition of (RS)-1-aminoindan-1,5-dicarboxylic acid and (RS)-alpha-cyclopropyl-4-phosphonophenylglycine, respectively. Collectively, the present study provided functional evidences for the involvement of mGluR4 in umami taste responses in mice. The results also suggest that T1R1 + T1R3 and mGluR1 are involved in umami taste responses in mice. Thus, umami taste would be mediated by multiple receptors.
机译:鲜味是由谷氨酸和其他一些氨基酸引起的,被认为是由G蛋白偶联受体引发的。提议的鲜味受体包括味觉受体1型,成员1和3(T1R1 + T1R3)的异二聚体,以及代谢型谷氨酸受体1和4(mGluR1和mGluR4)。积累的证据支持T1R1 + T1R3参与小鼠的鲜味反应。然而,关于mGluR在鲜味中的体内功能所知甚少。在这里,我们检查了野生型小鼠和遗传缺乏mGluR4(mGluR4-KO)的小鼠中的鼓膜鼓膜(CT)和舌咽(GL)神经的味觉反应。我们的结果表明,与野生型小鼠相比,mGluR4-KO小鼠在CT和CT上均显示出对谷氨酸和l-(+)-2-氨基-4-膦酰丁酸(III组mGluR的激动剂)的味觉神经反应明显较小。 GL神经不影响对其他味觉刺激的反应。 mGluR4-KO小鼠中的残留谷氨酸反应不受(RS)-α-环丙基-4-膦酰基苯甘氨酸(III型mGluR的拮抗剂)的影响,但在CT和(RS)-中被古马灵(一种T1R3阻断剂)抑制了。 CT和GL神经中的1-氨基茚满-1,5-二羧酸(I组mGluR的拮抗剂)。在野生型小鼠中,喹喹酸(I组mGluR的激动剂)和1-(+)-2-氨基-4-膦酸丁酸酯均引起味觉神经反应,并且通过添加(RS)-1-氨基茚满抑制这些反应。 -1,5-二羧酸和(RS)-α-环丙基-4-膦酰基苯基甘氨酸。总的来说,本研究为mGluR4参与小鼠鲜味味觉反应提供了功能性证​​据。结果还表明T1R1 + T1R3和mGluR1参与了小鼠的鲜味味道反应。因此,鲜味将由多种受体介导。

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