Team-Physiologie de la Nutrition & Toxicologie, U1231 INSERM/Université de Bourgogne-Franche Comté (UBFC)/Agro-Sup, Dijon, 21000, France.
Team-Physiologie de la Nutrition & Toxicologie, U1231 INSERM/Université de Bourgogne-Franche Comté (UBFC)/Agro-Sup, Dijon, 21000, France.
Biochimie. 2019 Apr;159:3-8. doi: 10.1016/j.biochi.2018.06.013. Epub 2018 Jun 22.
The choice of food is governed largely by the sense of taste. To date, five basic taste modalities have been described; however, there is an increasing agreement on the existence of a 6 fat taste. The taste modalities might interact with each other and also with other senses. The advancements in cellular and molecular biology have helped the characterization of taste signaling mechanisms, down to the receptor level and beyond. CD36 and GPR120 have been shown to be involved in the detection of fat taste while bitter taste is perceived by a number of receptors that belong to a family of taste-type 2 receptors (T2R or TAS2R). Hence, the most common role is played by TAS2R16 and TAS2R38 in bitter taste perception in humans. Increasing evidences from behavioural studies suggest that fat and bitter taste modalities might interact with each other, and this interaction might be critical in obesity. In the current review, we will discuss the evidence from genetic and behavioural studies and propose the molecular mechanism of a cross-talk between fat and bitter tastes.
食物的选择在很大程度上受味觉的支配。迄今为止,已经描述了五种基本的味觉模式;然而,人们越来越认同存在第六种脂肪味觉。味觉模式可能相互作用,也可能与其他感觉相互作用。细胞和分子生物学的进步有助于对味觉信号机制进行特征描述,甚至可以深入到受体水平及受体水平之后。已经表明 CD36 和 GPR120 参与了脂肪味觉的检测,而苦味则由属于味觉型 2 受体(T2R 或 TAS2R)家族的多个受体感知。因此,TAS2R16 和 TAS2R38 在人类苦味感知中起着最常见的作用。越来越多的行为研究证据表明,脂肪和苦味模式可能相互作用,这种相互作用在肥胖中可能是至关重要的。在当前的综述中,我们将讨论来自遗传和行为研究的证据,并提出脂肪和苦味之间相互作用的分子机制。