1. GABA B receptor signaling in the caudate putamen is involved in binge-like consumption during a high fat diet in mice.
- Author
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Sun R, Tsunekawa T, Hirose T, Yaginuma H, Taki K, Mizoguchi A, Miyata T, Kobayashi T, Sugiyama M, Onoue T, Takagi H, Hagiwara D, Ito Y, Iwama S, Suga H, Banno R, Bettler B, and Arima H
- Subjects
- Animals, Baclofen administration & dosage, Bulimia drug therapy, Bulimia genetics, Bulimia pathology, Diet, High-Fat adverse effects, Disease Models, Animal, Dopaminergic Neurons metabolism, Female, GABA-B Receptor Agonists administration & dosage, Humans, Male, Mice, Mice, Knockout, Mice, Transgenic, Nucleus Accumbens cytology, Nucleus Accumbens metabolism, Nucleus Accumbens pathology, Obesity etiology, Obesity prevention & control, Putamen cytology, Putamen metabolism, Putamen pathology, Receptors, Dopamine D1 metabolism, Receptors, G-Protein-Coupled genetics, Receptors, GABA-B genetics, Signal Transduction drug effects, Signal Transduction genetics, Bulimia physiopathology, Obesity physiopathology, Putamen physiopathology, Receptors, GABA-B metabolism
- Abstract
Previous studies suggest that signaling by the gamma-aminobutyric acid (GABA) type B receptor (GABA
B R) is involved in the regulation of binge eating, a disorder which might contribute to the development of obesity. Here, we show that intermittent access to a high fat diet (HFD) induced binge-like eating behavior with activation of dopamine receptor d1 (drd1)-expressing neurons in the caudate putamen (CPu) and nucleus accumbens (NAc) in wild-type (WT) mice. The activation of drd1-expressing neurons during binge-like eating was substantially increased in the CPu, but not in the NAc, in corticostriatal neuron-specific GABAB R-deficient knockout (KO) mice compared to WT mice. Treatment with the GABAB R agonist, baclofen, suppressed binge-like eating behavior in WT mice, but not in KO mice, as reported previously. Baclofen also suppressed the activation of drd1-expressing neurons in the CPu, but not in the NAc, during binge-like eating in WT mice. Thus, our data suggest that GABAB R signaling in CPu neurons expressing drd1 suppresses binge-like consumption during a HFD in mice., (© 2021. The Author(s).)- Published
- 2021
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