Toll-like receptor 4 mediates fat, sugar, and umami taste preference and food intake and body weight regulation.

Obesity (Silver Spring)

Laboratory of Neurosciences, National Institute on Aging, Intramural Research Program, Baltimore, Maryland, USA.

Published: July 2017

AI Article Synopsis

  • The study examines how Toll-like receptor 4 (TLR4) influences the taste preferences for fats and sugars in mice, connecting immune pathways to metabolic disorders.
  • TLR4 knockout mice displayed a lower preference for dietary lipids, sugars, and umami compared to wild-type mice, indicating that TLR4 plays a crucial role in taste perception.
  • Additionally, TLR4 KO mice on a high-fat, high-sugar diet consumed less and gained less weight, suggesting that TLR4 signaling enhances the intake of these unhealthy foods.

Article Abstract

Objective: Immune and inflammatory pathways play important roles in the pathogenesis of metabolic disorders. This study investigated the role of toll-like receptor 4 (TLR4) in orosensory detection of dietary lipids and sugars.

Methods: Taste preferences of TLR4 knockout (KO) and wild-type (WT) male mice under a standard and a high-fat, high-sugar diet were assessed with two-bottle tests. Gene expression of taste signaling molecules was analyzed in the tongue epithelium. The role of TLR4 in food intake and weight gain was investigated in TLR4 KO and WT mice fed a high-fat and high-sugar diet for 12 weeks.

Results: Compared to WT mice, TLR4 KO mice showed reduced preference for lipids, sugars, and umami in a two-bottle preference test. The altered taste perception was associated with decreased levels of key taste regulatory molecules in the tongue epithelium. TLR4 KO mice on a high-fat and high-sugar diet consumed less food and drink, resulting in diminished weight gain.

Conclusions: TLR4 signaling promotes ingestion of sugar and fat by a mechanism involving increased preference for such obesogenic foods.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487280PMC
http://dx.doi.org/10.1002/oby.21871DOI Listing

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