Centre des Sciences du Goût et de l'Alimentation, UMR-1324 INRA, UMR-6265 CNRS, Université de Bourgogne, 21000, Dijon, France.
Appl Microbiol Biotechnol. 2012 Nov;96(3):619-30. doi: 10.1007/s00253-012-4387-3. Epub 2012 Sep 18.
Sweet-tasting compounds are recognized by a heterodimeric receptor composed of the taste receptor, type 1, members 2 (T1R2) and 3 (T1R3) located in the mouth. This receptor is also expressed in the gut where it is involved in intestinal absorption, metabolic regulation, and glucose homeostasis. These metabolic functions make the sweet taste receptor a potential novel therapeutic target for the treatment of obesity and related metabolic dysfunctions such as diabetes. Existing sweet taste inhibitors or blockers that are still in development would constitute promising therapeutic agents. In this review, we will summarize the current knowledge of sweet taste inhibitors, including a sweet-taste-suppressing protein named gurmarin, which is only active on rodent sweet taste receptors but not on that of humans. In addition, their potential applications as therapeutic tools are discussed.
甜味化合物被位于口腔中的异型二聚体味觉受体 1 型成员 2(T1R2)和 3(T1R3)识别。该受体也在肠道中表达,参与肠道吸收、代谢调节和葡萄糖稳态。这些代谢功能使甜味受体成为治疗肥胖和相关代谢功能障碍(如糖尿病)的潜在新的治疗靶点。现有的甜味抑制剂或阻滞剂仍在开发中,将成为有前途的治疗药物。在这篇综述中,我们将总结甜味抑制剂的现有知识,包括一种名为gurmarin 的甜味抑制蛋白,它仅对啮齿动物的甜味受体有活性,而对人类的甜味受体没有活性。此外,还讨论了它们作为治疗工具的潜在应用。