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Dopamine D2 receptors in addiction-like reward dysfunction and compulsive eating in obese rats.肥胖大鼠成瘾样奖励功能障碍和强迫性进食中的多巴胺 D2 受体。
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食物强化的行为经济学以及预喂食、灭绝和依替必利对多巴胺 D2 受体突变小鼠的影响。

Behavioral economics of food reinforcement and the effects of prefeeding, extinction, and eticlopride in dopamine D2 receptor mutant mice.

机构信息

Department of Psychiatry and Behavioral Sciences, Division of Behavioral Biology, Johns Hopkins University, Ross 469, 720 Rutland Ave, Baltimore, MD 21205, USA.

出版信息

Psychopharmacology (Berl). 2011 Jun;215(4):775-84. doi: 10.1007/s00213-011-2173-z. Epub 2011 Feb 2.

DOI:10.1007/s00213-011-2173-z
PMID:21287342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3981201/
Abstract

RATIONALE

Several studies have investigated the reinforcing effects of food in genetically engineered mice lacking dopamine D(2) receptors (DA D(2)Rs); however, behavioral economic analyses quantifying reinforcement have not been conducted.

OBJECTIVE

The role of DA D(2)Rs in food reinforcement was examined by comparing responding under various fixed-ratio (FR) schedules of reinforcement, and effects of extinction, satiation, and the DA D(2)R antagonist eticlopride, in mice with and without genetic deletions of the receptor.

RESULTS

Response rates of DA D(2)R knockout (KO) mice were generally lower than those of littermate wild-type (WT) and heterozygous (HET) mice. The demand curve (consumption vs. FR value) for KO mice decreased more steeply than that of HET or WT mice, suggesting that reinforcing effectiveness is decreased with DA D(2)R deletion. Prefeeding decreased, whereas extinction increased overall response rates as a proportion of baseline, with no significant genotype differences. Both (+)- and (-)-eticlopride dose-dependently decreased responding in all genotypes with (-)-eticlopride more potent than (+)-eticlopride in all but KO mice. The enantiomers were equipotent in KO mice, and similar in potency to (+)-eticlopride in WT and HET mice.

CONCLUSIONS

That prefeeding and extinction did not vary across genotypes indicates a lack of involvement of DA D(2)Rs in these processes. Differences between (-)-eticlopride effects and extinction indicate that DA D(2)R blockade does not mimic extinction. The maintenance of responding in KO mice indicates that the DA D(2)R is not necessary for reinforcement. However, the economic analysis indicates that the DA D(2)R contributes substantially to the effectiveness of food reinforcement.

摘要

原理

已有多项研究调查了缺乏多巴胺 D2 受体(DA D2Rs)的基因工程小鼠中食物的强化效应;然而,尚未进行量化强化的行为经济学分析。

目的

通过比较不同固定比率(FR)强化方案下的反应以及在有和没有受体基因缺失的小鼠中进行的消退、饱食和 DA D2R 拮抗剂 eticlopride 的作用,研究 DA D2Rs 在食物强化中的作用。

结果

DA D2R 敲除(KO)小鼠的反应率通常低于同窝野生型(WT)和杂合子(HET)小鼠。KO 小鼠的需求曲线(消耗与 FR 值的关系)下降得比 HET 或 WT 小鼠更陡峭,这表明强化效力随 DA D2R 缺失而降低。预先喂食减少,而消退则增加了整体反应率,相对于基线,而基因型之间没有显著差异。(+)-和(-)-eticlopride 均以剂量依赖的方式降低了所有基因型的反应,而(-)-eticlopride 的作用比(+)-eticlopride 在除 KO 小鼠之外的所有小鼠中更为强烈。两种对映体在 KO 小鼠中均具有等效的效力,并且在 WT 和 HET 小鼠中的效力与(+)-eticlopride 相似。

结论

预喂食和消退在基因型之间没有差异表明 DA D2Rs 不参与这些过程。(-)-eticlopride 作用与消退之间的差异表明,DA D2R 阻断并不模拟消退。KO 小鼠中反应的维持表明 DA D2R 对于强化并非必需。然而,经济分析表明,DA D2R 对食物强化的有效性有很大贡献。