Citation: Wang Nan, Chai Guobi, Wang Dingzhong, Ji Lingbo, Zhao Wuduo, Cui Kai, Zong Yongli, Fan Wu, Liu Junhui. Astringent Compounds and Related Transduction Mechanisms[J]. Chemistry, ;2016, 79(12): 1134-1138,1133. shu

Astringent Compounds and Related Transduction Mechanisms

  • Corresponding author: Fan Wu,  Liu Junhui, 
  • Received Date: 26 May 2016
    Available Online: 18 August 2016

    Fund Project:

  • Astringent compounds are one of the predominant factors to the quality of foods and beverages. Research on astringency perception has attracted great interest over past decades due to its positive effects on the human body including antibacterial, anticarcinogenic, antioxidant, and neuroprotective effects. Astringency is described as a ‘drying, roughing, puckering and astringent sensation’ in the mouth following consumption of astringent compounds such as polyphenols. It is debated whether astringency is a taste sensation or tactile sensation, or a trigeminal sensation analogous to spicy taste. Studies on the mechanisms of astringency are based on protein precipitation theory. This paper gives a brief introduction of the astringent compounds and mechanisms of astringency perception.
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    1. [1]

      [1] C Clark, H Lawless. Chem. Senses., 1994, 19: 583~594.

    2. [2]

      [2] Standard definitions of terms relating to sensory evaluation of materials and products. Annual book of ASTM standards. Philadelphia: American Society for Testing and Materials, 2004.

    3. [3]

      [3] M Das, D R Bickers, H Mukhtar. Int. J. Cancer., 1989, 43: 468~470.

    4. [4]

      [4] M Athar, W A Khan, H Mukhtar. Cancer Res., 1989, 49: 5784~5788.

    5. [5]

      [5] A Scalbert. Phytochem., 1991, 30, 3875~3883.

    6. [6]

      [6] P L Teissedre, E N Frankel, A L Waterhouse et al. J. Sci. Food Agric., 1996, 70: 55~61.

    7. [7]

      [7] K Chung, T Y Wong, C Wei et al. Crit. Rev. Food Sci. Nutr., 1998, 38: 421~464.

    8. [8]

      [8] A Simonyi, D Woods, A Y Sun et al. Alcohol Clin. Exp. Res., 2002, 26: 352~357.

    9. [9]

      [9] M Ozeck, P Brust, H Xu et al. Eur. J. Pharmacol., 2004, 489: 139~149.

    10. [10]

      [10] S Ugawa, T Yamamoto, T Ueda et al. J. Neurosci., 2003, 23: 3616~3622.

    11. [11]

      [11] S Simon, W L Hall, S S Schiffman. Pharm. Biochem. Behav., 1992, 43: 271~283.

    12. [12]

      [12] Y Kawamura, M Funakoshi, Y Kasahara et al. Jpn. J. Physiol., 1969, 19: 851~865.

    13. [13]

      [13] S S Schiffman, M S Suggs, A L Sostman et al. Physiol. Behav., 1992, 51: 55~63.

    14. [14]

      [14] S Iiyama, S Ezaki, K Toko et al. Sens. Actuat. B Chem., 1995, 24: 75~79.

    15. [15]

      [15] E C Bate-Smith. Food, 1954, 23: 124~127.

    16. [16]

      [16] B Lyman, B Green. Chem. Senses, 1990, 15: 151~164.

    17. [17]

      [17] P Breslin, M Gilmore, G Beauchamp et al. Chem. Senses, 1993, 18: 405~417.

    18. [18]

      [18] J Lim, H T Lawless. Physiol. Behav., 2005, 85: 308~313.

    19. [19]

      [19] G Luck, H Liao, N J Murray et al. Phytochemistry, 1994, 37: 357~371.

    20. [20]

      [20] K S Feldman, A Sambandam, S T Lemon et al. Phytochemistry, 1999, 51: 867~872.

    21. [21]

      [21] E Jöbstl, J O'Connell, J P Fairclough et al. Biomacromolecules, 2004, 5: 942~949.

    22. [22]

      [22] N Schöbel, D Radtke, J Kyereme et al. Chem. Senses, 2014, 39: 471~87.

    23. [23]

      [23] M A Joslyn, J L Goldstein. Adv. Food Res., 1964, 13: 179~217.

    24. [24]

      [24] R A Arnold, A C Noble, V L Singleton. J. Agric. Food Chem., 1980, 28: 675~678.

    25. [25]

      [25] S Courregelongue, P Schlich, A C Noble. Food Qual. Pref., 1999, 10: 273~279.

    26. [26]

      [26] M Naish, M N Clifford, G G Birch. J. Sci. Food Agric., 1993, 61: 57~64.

    27. [27]

      [27] H Peleg, K Gacon, P Schlich et al. J. Sci. Food Agric., 1999, 79: 1123~1128.

    28. [28]

      [28] K H Gustavson. J. Polym. Sci., 1954, 12: 317~324.

    29. [29]

      [29] J L Goldstein, T Swain. Phytochemistry, 1963, 2: 371~383.

    30. [30]

      [30] W D Loomis, J Battaile. Phytochemistry, 1966, 5: 423~438.

    31. [31]

      [31] W D Loomis. Methods Enzymol., 1974, 31: 528~544.

    32. [32]

      [32] E Haslam. Biochem. J., 1974, 139: 285~288.

    33. [33]

      [33] A E Hagerman, L G Butler. J. Biol. Chem., 1981, 256: 4494~4497.

    34. [34]

      [34] C Simon, K Barathieu, M Laguerre et al. Biochemistry, 2003, 42: 10385~10395.

    35. [35]

      [35] R A Frazier, A Papadopoulou, R J Green. J. Pharm. Biomed. Anal., 2006, 41: 1602~1605.

    36. [36]

      [36] J L Goldstein, T Swain. Phytochemistry, 1965, 4: 185~192.

    37. [37]

      [37] H I Oh, J E Hoff, G S Armstrong et al. J. Agric. Food Chem., 1980, 28: 394~398.

    38. [38]

      [38] T Hatano, R W Hemingway. Chem. Commun., 1996: 2537~2538.

    39. [39]

      [39] K Wroblewski, R Muhandiram, A Chakrabartty et al. Eur. J. Biochem., 2001, 268: 4384~4397.

    40. [40]

      [40] E Jobstl, J R Howse, J P A Fairclough et al. J. Agric. Food Chem., 2006, 54: 4077~4081.

    41. [41]

      [41] K Yokotsuka, V L Singleton. Am. J. Enol. Vitic., 1995, 46: 329~338.

    42. [42]

      [42] N J Baxter, T H Lilley, E Haslam et al. Biochemistry, 1997, 36: 5566~5577.

    43. [43]

      [43] H Kawamoto, F Nakatsubo, K Murakami. Phytochemistry, 1995, 40: 1503~1505.

    44. [44]

      [44] A J Charlton, N J Baxter, M L Khan et al. J. Agric. Food Chem., 2002, 50: 1593~1601.

    45. [45]

      [45] U Fischer, R B Boulton, A C Noble. Food Qual. Pref., 1994, 5: 55~64.

    46. [46]

      [46] S Kallithraka, J Bakker, M N Clifford. J. Agric. Food Chem., 1997, 45: 2211~2216.

    47. [47]

      [47] H Peleg, K K Bodine, A C Noble. Chem. Senses, 1998, 23: 371~378.

    48. [48]

      [48] H Peleg, A C Noble. Food Qual. Pref., 1999, 100: 343~347.

    49. [49]

      [49] R A Sowalsky, A C Noble. Chem. Senses, 1998, 23: 343~349.

    50. [50]

      [50] S Martin, R M Pangborn. J. Dent. Res. 1971, 50: 485~490.

    51. [51]

      [51] R J Hyde, R M Pangborn. Am. J. Enol. Vitic., 1978, 29: 87~91.

    52. [52]

      [52] S M Rubico, M R McDaniel. Chem. Senses, 1992, 17: 273~289.

    53. [53]

      [53] P Hartwig, M R Mc Daniel. J. Food Sci., 1995, 60: 384~388.

    54. [54]

      [54] C H Corrigan, H T Lawless. Chem. Senses, 1995, 20:593~600.

    55. [55]

      [55] C A Lee, B Ismail, Z M Vickers. J. Food Sci. 2012, 77: 381~387.

    56. [56]

      [56] H T Lawless, J Horne, P Giasi. Chem. Senses, 1996, 21: 397~403.

    57. [57]

      [57] G A Trapp. J. Environ. Pathol. Tox., 1985, 6, 15.

    58. [58]

      [58] M W Dodds, D A Johnson, C K Yeh. J. Dent. Res., 2005, 33: 223~233.

    59. [59]

      [59] Q Yan, A Bennick. Biochem. J., 1995, 311: 341~347.

    60. [60]

      [60] Y Lu, A Bennick. Arch. Oral Biol., 1998, 43:717~728.

    61. [61]

      [61] V de Freitas, N Mateus. J. Sci. Food Agric., 2001, 82: 113~119.

    62. [62]

      [62] A Gambuti, A Rinaldi, R Pessina et al. Food Chem., 2006, 97: 614~620.

    63. [63]

      [63] N Condelli, A Dinnella, A Cerone et al. Food Qual. Pref., 2006, 17: 96~107.

    64. [64]

      [64] B L Slomiany, V L N Murty. J Piotrowski et al. Gen. Pharmacol., 1996, 27: 761~771.

    65. [65]

      [65] H Inoue, K Ono, W Masuda et al. J. Oral Biosci., 2008, 50: 134~141.

    66. [66]

      [66] H Boze, T Marlin, D Durand et al. Biophys. J., 2010, 99: 656~665.

    67. [67]

      [67] R Pramanik, S M Osailan, S J Challacombe et al. Eur. J. Oral Sci., 2010, 118: 245~253.

    68. [68]

      [68] S D Bradway, E J Bergey, P C Jones et al. Biochem. J., 1989, 261: 887~896.

    69. [69]

      [69] A J Charlton, N J Baxter, M L Khan et al. J. Agric. Food Chem., 2002, 50: 593~1601.

    70. [70]

      [70] J F Prinz, R A de Wijk, L Huntjens. Food Hydrocoll., 2006, 21: 402~408.

    71. [71]

      [71] N Brossard, H Cai, F Osorio et al. J. Texture Stud., 2016, doi: 10.1111/jtxs.12184

    72. [72]

      [72] S Ma, H Lee, Y Liang et al. Angew. Chem. Int. Ed., 2016, 55: 5793~5797.

    73. [73]

      [73] M Kurogi, M Miyashita, Y Emoto et al. Chem. Senses., 2012, 37: 167~177.

    74. [74]

      [74] H L Gibbins, G H Carpenter. J. Texture Stud., 2013, 44: 364~375.

    75. [75]

      [75] G Ares, C Barreiro, R Deliza et al. Food Res. Int., 2009, 42: 871~878.

    76. [76]

      [76] B J Lyman, B G Green. Chem. Senses, 1990, 15: 151~164.

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