Synapse · 2018 · 32 citations · 75 references
MedicineNeurosciencePharmacologyNeurochemistryNeuroendocrinologyNeuropharmacologyAppetite RegulationDopaminergic PharmacologyDopaminergic SignalingObesity ManagementReward PathwaysWeight ManagementD1-like Dopamine ReceptorsDopamine D1-like ReceptorsDopamine TransportersDopaminergic Pathway RegulationDopaminergic System EffectsMesocortical Dopamine SystemReward Pathway DysregulationSham Treatment
Abstract Roux‐en‐Y gastric bypass surgery (RYGB) is one of the most effective treatments for morbid obesity. However, increased substance abuse following RYGB has been observed clinically. This study examined the effects of RYGB on the dopamine system to elucidate these observed changes in reward‐related behavior. Rats were assigned to four groups: normal diet with sham surgery, ad libitum high fat (HF) diet with sham surgery, restricted HF diet with sham surgery, and HF diet with RYGB surgery. Following surgeries, rats were kept on their respective diets for 9 weeks before they were sacrificed. [ 3 H]SCH 23390, [ 3 H]Spiperone, and [ 3 H]WIN35 428 autoradiography was performed to quantify the effects of diet and RYGB surgery on dopamine type 1‐like receptor (D1R)‐like, dopamine type 2‐like receptor (D2R)‐like, and dopamine transporter (DAT) binding. Rats on a chronic HF diet became obese with reduced D1R‐like binding within the ventrolateral striatum and the nucleus accumbens core, reduced D2R‐like binding in all areas of the striatum and nucleus accumbens core and shell, and reduced DAT binding in the dorsomedial striatum. Restricted HF diet rats showed similar reductions in D1R‐like and D2‐R‐like binding as the obese rats, and reduced DAT binding within all areas of the striatum. Both RYGB and restricted HF diet rats showed similar weight reductions, with RYGB rats showing no difference in binding compared to controls. The observed changes in binding between non‐treated obese rats and RYGB rats demonstrates that HF dietary effects on the dopamine system were reversed by RYGB.
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