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多巴胺、摄食激活和反应效果评估:关注单次 session 内舔吸爆发次数的时程变化。

Dopamine, activation of ingestion and evaluation of response efficacy: a focus on the within-session time-course of licking burst number.

机构信息

Dipartimento di Scienze Biomediche, Università di Sassari, Viale S. Pietro 43/b, Sassari, 07100, Italy.

出版信息

Psychopharmacology (Berl). 2024 Jun;241(6):1111-1124. doi: 10.1007/s00213-024-06600-1. Epub 2024 May 4.

Abstract

RATIONALE

Evidence on the effect of dopamine D1-like and D2-like receptor antagonists on licking microstructure and the forced swimming response led us to suggest that (i) dopamine on D1-like receptors plays a role in activating reward-directed responses and (ii) the level of response activation is reboosted based on a process of evaluation of response efficacy requiring dopamine on D2-like receptors. A main piece of evidence in support of this hypothesis is the observation that the dopamine D2-like receptor antagonist raclopride induces a within-session decrement of burst number occurring after the contact with the reward. The few published studies with a detailed analysis of the time-course of this measure were conducted in our laboratory.

OBJECTIVES

The aim of this review is to recapitulate and discuss the evidence in support of the analysis of the within-session burst number as a behavioural substrate for the study of the mechanisms governing ingestion, behavioural activation and the related evaluation processes, and its relevance in the analysis of drug effects on ingestion.

CONCLUSIONS

The evidence gathered so far suggests that the analysis of the within-session time-course of burst number provides an important behavioural substrate for the study of the mechanisms governing ingestion, behavioural activation and the related evaluation processes, and might provide decisive evidence in the analysis of the effects of drugs on ingestion. However, further evidence from independent sources is necessary to validate the use and the proposed interpretation of this measure.

摘要

原理

有关多巴胺 D1 样和 D2 样受体拮抗剂对舔舐微观结构和强迫游泳反应影响的证据使我们提出,(i)多巴胺在 D1 样受体上的作用在于激活奖励导向的反应,(ii)反应激活的水平根据需要 D2 样受体上的多巴胺的反应效能评估过程重新增强。支持这一假设的一个主要证据是观察到多巴胺 D2 样受体拮抗剂氯丙嗪在与奖励接触后会导致爆发次数在会话期间内减少。我们实验室进行了一些关于该措施时间进程的详细分析的已发表研究。

目的

本综述的目的是回顾和讨论支持分析会话内爆发次数作为研究控制摄入、行为激活和相关评估过程的机制的行为底物的证据,及其在分析药物对摄入的影响方面的相关性。

结论

迄今为止收集的证据表明,分析爆发次数的会话内时间进程为研究控制摄入、行为激活和相关评估过程的机制提供了重要的行为底物,并可能为分析药物对摄入的影响提供决定性证据。然而,需要来自独立来源的进一步证据来验证该措施的使用和提出的解释。

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