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Molecular mechanisms of human fat taste perception

Project

Food and consumer protection

This project contributes to the research aim 'Food and consumer protection'. Which funding institutions are active for this aim? What are the sub-aims? Take a look:
Food and consumer protection


Project code: keine Angaben
Contract period: 01.01.2009 - 31.12.2012
Purpose of research: Applied research

The objective of this sub-project was to investigate the molecular mechanisms underlying human taste perception of fat, in order to characterize the multifactorial flavor evoked by fats in cooperation with other cluster participants. Besides carbohydrates and proteins, fats are the main energy providing food components and are considered as one of the main riskfactors for the development of obesity and related diseases in industrialized countries. Risk-lowering strategies including the reduction of fat contents in dietary products did not succeed so far because consumers were left with unsatisfying taste impressions. For a long time the recognition of fat was believed to rely mostly on textural, olfactory and post-ingestive cues. However, during the recent years research performed in rodent models revealed an additional gustatory component for the detection of, in particular, long-chain fatty acids. In contrast to this, much less is known about fat taste perception in humans. In agreement with the above mentioned rodent studies, sensory studies performed by the group of Prof. Hofmann (sub-project 6 A) revealed long-chain fatty acids as predominant fat taste stimuli also for human individuals. Therefore, we screened candidate fatty acid receptors in in vitro expression studies to correlate their pharmacological properties with the sensory results. It turned out that the pharmacological characteristics of the long-chain fatty acid receptors GPR40 and GPR120 are well correlated with the sensory properties assessed in sub-project 6 A. Especially the activation pattern of GPR120 matched specifically the “fatty” sensation elicited by long-chain fatty acids in sensory studies and is not responsible for the “scratchy” sensation of fatty acids and their alcohols. Further, we analyzed different human taste tissues and found the GPR120 receptor expressed in circumvallate and fungiform papillae. The receptor’s messenger (m)RNA and protein indeed were localized in taste bud cells as well as surrounding tongue epithelium. We demonstrated that a short splice variant, but not the long variant of GPR120, is expressed in taste tissue. We could also show that this variant is able to couple to different G-Proteins, among them Gustducin, which tranduces signals in taste cells. Consequently, the results of this project show that GPR120 indeed represents one of the receptor participating likely in human gustatory fatty acid perception. In the future this knowledge should help to design better acceptable low-fat foods.

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