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鲜味的味觉受体:多种受体的情况

Taste receptors for umami: the case for multiple receptors.

作者信息

Chaudhari Nirupa, Pereira Elizabeth, Roper Stephen D

机构信息

Department of Physiology and Biophysics, University of Miami, FL 33136, USA.

出版信息

Am J Clin Nutr. 2009 Sep;90(3):738S-742S. doi: 10.3945/ajcn.2009.27462H. Epub 2009 Jul 1.

Abstract

Umami taste is elicited by many small molecules, including amino acids (glutamate and aspartate) and nucleotides (monophosphates of inosinate or guanylate, inosine 5'-monophosphate and guanosine-5'-monophosphate). Mammalian taste buds respond to these diverse compounds via membrane receptors that bind the umami tastants. Over the past 15 y, several receptors have been proposed to underlie umami detection in taste buds. These receptors include 2 glutamate-selective G protein-coupled receptors, mGluR4 and mGluR1, and the taste bud-expressed heterodimer T1R1+T1R3. Each of these receptors is expressed in small numbers of cells in anterior and posterior taste buds. The mGluRs are activated by glutamate and certain analogs but are not reported to be sensitive to nucleotides. In contrast, T1R1+T1R3 is activated by a broad range of amino acids and displays a strongly potentiated response in the presence of nucleotides. Mice in which the Grm4 gene is knocked out show a greatly enhanced preference for umami tastants. Loss of the Tas1r1 or Tas1R3 genes is reported to depress but not eliminate neural and behavioral responses to umami. When intact mammalian taste buds are apically stimulated with umami tastants, their functional responses to umami tastants do not fully resemble the responses of a single proposed umami receptor. Furthermore, the responses to umami tastants persist in the taste cells of T1R3-knockout mice. Thus, umami taste detection may involve multiple receptors expressed in different subsets of taste cells. This receptor diversity may underlie the complex perception of umami, with different mixtures of amino acids, peptides, and nucleotides yielding subtly distinct taste qualities.

摘要

鲜味是由许多小分子引发的,包括氨基酸(谷氨酸和天冬氨酸)和核苷酸(肌苷酸或鸟苷酸的单磷酸盐、5'-肌苷酸和5'-鸟苷酸)。哺乳动物的味蕾通过与鲜味剂结合的膜受体对这些不同的化合物作出反应。在过去15年里,已经提出了几种受体作为味蕾中鲜味检测的基础。这些受体包括2种谷氨酸选择性G蛋白偶联受体,即代谢型谷氨酸受体4(mGluR4)和代谢型谷氨酸受体1(mGluR1),以及味蕾中表达的异二聚体T1R1+T1R3。这些受体中的每一种都在前部和后部味蕾的少量细胞中表达。代谢型谷氨酸受体被谷氨酸和某些类似物激活,但据报道对核苷酸不敏感。相比之下,T1R1+T1R3被多种氨基酸激活,并且在存在核苷酸的情况下显示出强烈增强的反应。Grm4基因敲除的小鼠对鲜味剂的偏好大大增强。据报道,Tas1r1或Tas1R3基因的缺失会降低但不会消除对鲜味的神经和行为反应。当完整的哺乳动物味蕾用鲜味剂进行顶端刺激时,它们对鲜味剂的功能反应并不完全类似于单个提出的鲜味受体的反应。此外,对鲜味剂的反应在T1R3基因敲除小鼠的味觉细胞中持续存在。因此,鲜味检测可能涉及在不同味觉细胞亚群中表达的多种受体。这种受体多样性可能是鲜味复杂感知的基础,不同的氨基酸、肽和核苷酸混合物会产生微妙不同的味觉品质。

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