Department of Molecular Genetics, German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany.
Chem Senses. 2012 Feb;37(2):123-39. doi: 10.1093/chemse/bjr069. Epub 2011 Aug 25.
In contrast to carbohydrates and proteins, which are detected by specialized taste receptors in the forms of their respective building blocks, sugars, and L-amino acids, the third macronutrient, lipids, has until now not been associated with gustatory receptors. Instead, the recognition of fat stimuli was believed to rely mostly on textural, olfactory, and postingestive cues. During the recent years, however, research done mainly in rodent models revealed an additional gustatory component for the detection of long-chain fatty acids (LCFAs), the main taste-activating component of lipids. Concomitantly, a number of candidate fat taste receptors were proposed to be involved in rodent's gustatory fatty acid perception. Compared with rodent models, much less is known about human fat taste. In order to investigate the ability of the human gustatory system to respond to fat components, we performed sensory experiments with fatty acids of different chain lengths and derivatives thereof. We found that our panelists discriminated a "fatty" and an irritant "scratchy" taste component, with the "fatty" percept restricted to LCFAs. Using functional calcium-imaging experiments with the human orthologs of mouse candidate fat receptors belonging to the G protein-coupled receptor family, we correlated human sensory data with receptor properties characterized in vitro. We demonstrated that the pharmacological activation profile of human GPR40 and GPR120, 2 LCFA-specific receptors associated with gustatory fat perception in rodents, is inconsistent with the "scratchy" sensation of human subjects and more consistent with the percept described as "fatty." Expression analysis of GPR40 and GPR120 in human gustatory tissues revealed that, while the GPR40 gene is not expressed, GPR120 is detected in gustatory and nongustatory epithelia. On a cellular level, we found GPR120 mRNA and protein in taste buds as well as in the surrounding epithelial cells. We conclude that GPR120 may indeed participate in human gustatory fatty acid perception.
与碳水化合物和蛋白质不同,它们分别以各自的结构单元——糖和 L-氨基酸的形式被专门的味觉受体所感知,直到现在,作为第三大宏量营养素的脂肪还没有与味觉受体联系起来。相反,人们认为脂肪刺激物的识别主要依赖于质地、嗅觉和摄食后线索。然而,近年来,主要在啮齿动物模型中进行的研究揭示了长链脂肪酸(LCFAs)检测的另一个味觉成分,LCFAs 是脂质的主要味觉激活成分。同时,提出了一些候选脂肪味觉受体参与啮齿动物的味觉脂肪酸感知。与啮齿动物模型相比,人们对人类脂肪味觉的了解要少得多。为了研究人类味觉系统对脂肪成分的反应能力,我们用不同链长的脂肪酸及其衍生物进行了感官实验。我们发现,我们的小组人员能够区分出一种“脂肪”和一种刺激性的“刺痛”味道成分,而“脂肪”感知仅限于 LCFAs。使用属于 G 蛋白偶联受体家族的候选脂肪受体的人类同源物的功能性钙成像实验,我们将人类的感官数据与体外特征化的受体特性相关联。我们证明,与人类受试者的“刺痛”感觉不一致,而与描述为“脂肪”的感觉更一致的是,人类 GPR40 和 GPR120 的药理学激活特征,这两种 LCFA 特异性受体与啮齿动物的味觉脂肪感知有关联。GPR40 和 GPR120 在人类味觉组织中的表达分析表明,虽然 GPR40 基因不表达,但 GPR120 在味觉和非味觉上皮中都有检测到。在细胞水平上,我们在味蕾以及周围的上皮细胞中发现了 GPR120 mRNA 和蛋白。我们得出结论,GPR120 确实可能参与人类味觉脂肪酸的感知。