The Human Bitter Taste Receptor hTAS2R50 Is Activated by the Two Natural Bitter Terpenoids Andrographolide and Amarogentin

被引:63
作者
Behrens, Maik [1 ]
Brockhoff, Anne [1 ]
Batram, Claudia [1 ]
Kuhn, Christina [1 ]
Appendino, Giovanni [2 ]
Meyerhof, Wolfgang [1 ]
机构
[1] German Inst Human Nutr Potsdam Rehbrucke, Dept Mol Genet, D-14558 Nuthetal, Germany
[2] Univ Piemonte, Dipartimento Sci Chim, I-28100 Novara, Italy
关键词
Bitter taste; TAS2Rs; heterologous expression; andrographolide; amarogentin; CELLS; PHENYLTHIOCARBAMIDE; SENSITIVITY; SUPPRESSION; EXPRESSION; SACCHARIN; PATHWAY; PROTEIN; GENES;
D O I
10.1021/jf9014334
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Bitterness perception in mammals is mediated through activation of dedicated bitter taste receptors located in the oral cavity. Genomic analyses revealed the existence of orthologous mammalian bitter taste receptor genes, which presumably recognize the same compounds in different species, as well as species-specific receptor gene expansions believed to fulfill a critical role during evolution. In man, 8 of the 25 bitter taste receptors (hTAS2Rs) are closely related members of such an expanded subfamily of receptor genes. This study identified two natural bitter terpenoids, andrographolide and amarogentin, that are agonists for the orphan receptor hTAS2R50, the most distant member of the subfamily. This paper presents the pharmacological characterization of this receptor and analyzes its functional relationship with the previously deorphaned hTAS2R43, hTAS2R44, hTAS2R46, and hTAS2R47. Insights into the general breadth of tuning, functional redundancies, and relationships between pharmacological activation patterns and amino acid homologies for this receptor subfamily are presented.
引用
收藏
页码:9860 / 9866
页数:7
相关论文
共 28 条
  • [1] Ammon C., 2002, Archives of Physiology and Biochemistry, V110, P137, DOI 10.1076/apab.110.1.137.908
  • [2] The human taste receptor hTAS2R14 responds to a variety of different bitter compounds
    Behrens, M
    Brockhoff, A
    Kuhn, C
    Bufe, B
    Winnig, M
    Meyerhof, W
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 319 (02) : 479 - 485
  • [3] Gustatory expression pattern of the human TAS2R bitter receptor gene family reveals a heterogenous population of bitter responsive taste receptor cells
    Behrens, Maik
    Foerster, Susann
    Staehler, Frauke
    Raguse, Jan-Dirk
    Meyerhof, Wolfgang
    [J]. JOURNAL OF NEUROSCIENCE, 2007, 27 (46) : 12630 - 12640
  • [4] BELITZ H-D, 1985, Food Reviews International, V1, P271, DOI 10.1080/87559128509540773
  • [5] Broad tuning of the human bitter taste receptor hTAS2R46 to various sesquiterpene lactones, clerodane and labdane diterpenoids, strychnine, and denatonium
    Brockhoff, Anne
    Behrens, Maik
    Massarotti, Alberto
    Appendino, Giovanni
    Meyerhof, Wolfgang
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2007, 55 (15) : 6236 - 6243
  • [6] The human TAS2R16 receptor mediates bitter taste in response to β-glucopyranosides
    Bufe, B
    Hofmann, T
    Krautwurst, D
    Raguse, JD
    Meyerhof, W
    [J]. NATURE GENETICS, 2002, 32 (03) : 397 - 401
  • [7] The molecular basis of individual differences in phenylthiocarbamide and propylthiouracil bitterness perception
    Bufe, B
    Breslin, PAS
    Kuhn, C
    Reed, DR
    Tharp, CD
    Slack, JP
    Kim, UK
    Drayna, D
    Meyerhof, W
    [J]. CURRENT BIOLOGY, 2005, 15 (04) : 322 - 327
  • [8] T2Rs function as bitter taste receptors
    Chandrashekar, J
    Mueller, KL
    Hoon, MA
    Adler, E
    Feng, LX
    Guo, W
    Zuker, CS
    Ryba, NJP
    [J]. CELL, 2000, 100 (06) : 703 - 711
  • [9] Andrographolide suppresses endothelial cell apoptosis via activation of phosphatidyl inositol-3-kinase/Akt pathway
    Chen, JH
    Hsiao, G
    Lee, AR
    Wu, CC
    Yen, MH
    [J]. BIOCHEMICAL PHARMACOLOGY, 2004, 67 (07) : 1337 - 1345
  • [10] Mechanisms of suppression of inducible nitric oxide synthase (iNOS) expression in RAW 264.7 cells by andrographolide
    Chiou, WF
    Chen, CF
    Lin, JJ
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2000, 129 (08) : 1553 - 1560