| First Author | Khan MSH | Year | 2025 |
| Journal | Mol Metab | Volume | 91 |
| Pages | 102068 | PubMed ID | 39571902 |
| Mgi Jnum | J:360669 | Mgi Id | MGI:7789778 |
| Doi | 10.1016/j.molmet.2024.102068 | Citation | Khan MSH, et al. (2024) FGF21 acts in the brain to drive macronutrient-specific changes in behavioral motivation and brain reward signaling. Mol Metab 91:102068 |
| abstractText | OBJECTIVE: Dietary protein restriction induces adaptive changes in food preference, increasing protein consumption over carbohydrates or fat. We investigated whether motivation and reward signaling underpin these preferences. METHODS AND RESULTS: In an operant task, protein-restricted male mice responded more for liquid protein rewards, but not carbohydrate, fat, or sweet rewards compared to non-restricted mice. When the number of responses required to access protein reward varied, protein-restricted mice exhibited higher operant responses at moderate to high response requirements. The protein restriction-induced increase in operant responding for protein was absent in Fgf21-KO mice and mice with neuron-specific deletion of the FGF21 co-receptor beta-Klotho (Klb(Cam2ka)). Fiber photometry recording of VTA dopamine neurons revealed that oral delivery of maltodextrin triggered a larger dopamine neuron activation than casein in control diet-fed mice, while casein triggered a larger activation in low-protein diet-fed mice. This restriction-induced shift in nutrient-specific VTA dopamine signaling was lost in Fgf21-KO mice. CONCLUSION: These data suggest that the increased FGF21 during protein restriction acts in the brain to induce a protein-specific appetite by specifically enhancing the reward value of protein-containing foods and the motivation to consume them. |
