Gut T1R3 sweet taste receptors do not mediate sucrose-conditioned flavor preferences in mice

被引:75
|
作者
Sclafani, Anthony [1 ]
Glass, Damien S. [1 ]
Margolskee, Robert F. [2 ]
Glendinning, John I. [3 ]
机构
[1] CUNY Brooklyn Coll, Dept Psychol, Brooklyn, NY 11210 USA
[2] Monell Chem Senses Ctr, Philadelphia, PA 19104 USA
[3] Columbia Univ Barnard Coll, Dept Biol Sci, New York, NY 10027 USA
关键词
flavor learning; sucralose; gastric infusions; T1R3 knockout mouse; ALPHA-GUSTDUCIN; UMAMI TASTE; 129P3/J MICE; FOOD REWARD; GLUCOSE; RATS; EXPRESSION; BITTER; CELLS; SUGAR;
D O I
10.1152/ajpregu.00495.2010
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Sclafani A, Glass DS, Margolskee RF, Glendinning JI. Gut T1R3 sweet taste receptors do not mediate sucrose-conditioned flavor preferences in mice. Am J Physiol Regul Integr Comp Physiol 299: R1643-R1650, 2010. First published October 6, 2010; doi:10.1152/ajpregu.00495.2010.-Most mammals prefer the sweet taste of sugars, which is mediated by the heterodimeric T1R2 + T1R3 taste receptor. Sugar appetite is also enhanced by the post-oral reinforcing actions of the nutrient in the gut. Here, we examined the contribution of gut T1R3 (either alone or as part of the T1R3 + T1R3 receptor) to post-oral sugar reinforcement using a flavor-conditioning paradigm. We trained mice to associate consumption of a flavored solution (CS+) with intragastric (IG) infusions of a sweetener, and a different flavored solution (CS-) with IG infusions of water (23 h/day); then, we measured preference in a CS+ vs. CS-choice test. In experiment 1, we predicted that if activation of gut T1R3 mediates sugar reinforcement, then IG infusions of a nutritive (sucrose) or nonnutritive (sucralose) ligand for this receptor should condition a preference for the CS+ in B6 wild-type (WT) mice. While the mice that received IG sucrose infusions developed a strong preference for the CS+, those that received IG sucralose infusions developed a weak avoidance of the CS+. In experiment 2, we used T1R3 knockout (KO) mice to examine the necessity of gut T1R2 + T1R3 receptors for conditioned flavor preferences. If intact gut T1R3 (or T1R2 + T1R3) receptors are necessary for flavor-sugar conditioning, then T1R3 KO mice should not develop a sugar-conditioned flavor preference. We found that T1R3 KO mice, like WT mice, acquired a strong preference for the CS+ paired with IG sucrose infusions. The KO mice were also like WT mice in avoiding a CS+ flavor paired with IG sucralose infusions These findings provide clear evidence that gut T1R3 receptors are not necessary for sugar-conditioned flavor preferences or sucralose-induced flavor avoidance in mice.
引用
下载
收藏
页码:R1643 / R1650
页数:8
相关论文
共 50 条
  • [21] T1R3 is a Receptor for the Taste of Calcium and Magnesium
    Tordoff, Michael G.
    Shao, Hongguang
    Alarcon, Laura K.
    Margolskee, Robert F.
    Mosinger, Bedrich
    Bachmanov, Alexander A.
    Reed, Danielle R.
    McCaughey, Stuart
    CHEMICAL SENSES, 2008, 33 (08) : S113 - S114
  • [22] Phosphorus Taste Involves T1R2 and T1R3
    Tordoff, Michael G.
    CHEMICAL SENSES, 2017, 42 (05) : 425 - 433
  • [23] Expression and Distribution of the Sweet Taste Receptor Isoforms T1R2 and T1R3 in Human and Rat Bladders
    Elliott, Ruth A.
    Kapoor, Shalini
    Tincello, Douglas G.
    JOURNAL OF UROLOGY, 2011, 186 (06): : 2455 - 2462
  • [24] T1R2, T1R3, and the Detection of Sweet Stimuli
    Vigues, Stephan
    Hobbs, Jeanette R.
    Nie, Yiling
    Conn, Graeme L.
    Munger, Steven D.
    SWEETNESS AND SWEETENERS: BIOLOGY, CHEMISTRY, AND PSYCHOPHYSICS, 2008, 979 : 65 - 75
  • [25] Sensitivity of human sweet taste receptor subunits T1R2 and T1R3 to activation by glucose enantiomers
    Dubovski, Nitzan
    Ben-Shoshan Galeczki, Yaron
    Malach, Einav
    Niv, Masha Y.
    CHEMICAL SENSES, 2023, 48
  • [26] Red algae-derived isofloridoside activates the sweet taste receptor T1R2/ T1R3
    Akishino, Miku
    Aoki, Yuko
    Baba, Hajime
    Asakawa, Makio
    Hama, Yoichiro
    Mitsutake, Susumu
    FOOD BIOSCIENCE, 2022, 50
  • [27] Anticonvulsant activity of artificial sweeteners: A structural link between sweet-taste receptor T1R3 and brain glutamate receptors
    Talevi, Alan
    Enrique, Andrea V.
    Bruno-Blanch, Luis E.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2012, 22 (12) : 4072 - 4074
  • [28] Neural taste responses to ethanol in C57BL/6J and T1R3 sweet taste receptor knockout mice
    Lemon, C. H.
    Brasser, S. M.
    ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2008, 32 (06) : 147A - 147A
  • [29] Systematic analysis reveals novel insight into the molecular determinants of function, diversity and evolution of sweet taste receptors T1R2/T1R3 in primates
    Wang, Congrui
    Liu, Yi
    Cui, Meng
    Liu, Bo
    FRONTIERS IN MOLECULAR BIOSCIENCES, 2023, 10
  • [30] Activation of the sweet taste receptor, T1R3, by the artificial sweetener sucralose regulates the pulmonary endothelium
    Harrington, Elizabeth O.
    Vang, Alexander
    Braza, Julie
    Shil, Aparna
    Chichger, Havovi
    AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2018, 314 (01) : L165 - L176