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Role of dopamine D1 and D2 receptors in the nucleus accumbens shell on the acquisition and expression of fructose-conditioned flavor-flavor preferences in rats

机译:多巴胺D1和D2受体在伏伏核壳中对大鼠果糖条件性风味偏好的获取和表达的作用

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摘要

Systemic administration of dopamine D1 () and less so D2 (raclopride) receptor antagonists significantly reduce acquisition and expression of fructoseconditioned flavor preferences (CFP). Because dopamine in the nucleus accumbens shell (NAcS) is implicated in food reward, the present study examined whether NAcS D1 or D2 antagonists altered acquisition and/or expression of fructose-CFP. In Experiment 1, food-restricted rats with bilateral NAcS cannulae were trained to drink a fructose (8%) + saccharin (0.2%) solution mixed with one flavor (CS+/Fs) and a less-preferred 0.2% saccharin solution with mixed another flavor (CS−/s). Unlimited two-bottle tests with the two flavors in saccharin (0.2%: CS+/s, CS−/s) occurred 10 min following total bilateral NAcS doses of 0, 12, 24 or 48 nmol of or raclopride. Preference for CS+/s over CS−/s following vehicle treatment (76%) was significantly reduced by (48 nmol, 62%) and raclopride (24 nmol, 63%). In Experiment 2, rats received bilateral NAcS injections (12 nmol) of or raclopride on one-bottle training (16 ml) days. Yoked control rats received vehicle and were limited to the CS intakes of the D1 and D2 groups, whereas untreated controls without injections received their CS ration during training. Subsequent unlimited two-bottle tests revealed initial preferences of CS+/s over CS−/s in all groups that remained stable in untreated and yoked controls, but were lost over the 6 tests sessions in D1 and D2 groups. These data indicate that NAcS D1 and D2 antagonists significantly attenuated the expression of the fructose-CFP and did not block acquisition, but hastened extinction of fructose-CFP.
机译:多巴胺D1()和D2(雷氯必利)受体拮抗剂的全身给药显着降低了果糖条件风味偏好(CFP)的获取和表达。因为伏隔核壳(NAcS)中的多巴胺与食物报酬有关,所以本研究检查了NAcS D1或D2拮抗剂是否改变了果糖CFP的获得和/或表达。在实验1中,训练有食物限制的双侧NAcS插管大鼠喝果糖(8%)+糖精(0.2%)溶液与一种风味剂(CS + / Fs)混合,而偏爱的0.2%糖精溶液与另一种风味剂混合风味(CS- / s)。在总的双侧NAcS剂量为0、12、24或48 nmol或raclopride后,糖精中的两种风味剂(0.2%:CS + / s,CS- / s)进行了无限制的两瓶试验(0.2%)。媒介物处理后(76%)相对于CS- / s的CS + / s偏好显着降低(48 nmol,62%)和雷洛必利(24 nmol,63%)。在实验2中,大鼠接受一瓶训练(16 ml)的双侧NAcS注射(12 nmol)或raclopride注射。轭对照组大鼠接受媒介物,并且仅限于D1和D2组的CS摄入量,而未经注射的未经治疗的对照组在训练过程中接受CS定量。随后的无限制两瓶试验显示,所有组中CS + / s优于CS- / s的初始偏好在未经治疗和带轭的对照组中均保持稳定,但在D1和D2组的6次试验中均消失了。这些数据表明,NAcS D1和D2拮抗剂可显着减弱果糖CFP的表达,并且不会阻止获取,但会加速果糖CFP的灭绝。

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