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体外增强海马体爆发活动:探寻斯金纳的行为基本单位

In vitro reinforcement of hippocampal bursting: a search for Skinner's atoms of behavior.

作者信息

Stein L, Xue B G, Belluzzi J D

机构信息

Department of Pharmacology, University of California, Irvine 92717.

出版信息

J Exp Anal Behav. 1994 Mar;61(2):155-68. doi: 10.1901/jeab.1994.61-155.

Abstract

A novel "in vitro reinforcement" paradigm was used to investigate Skinner's (1953) hypotheses (a) that operant behavior is made up of infinitesimal "response elements" or "behavioral atoms" and (b) that these very small units, and not whole responses, are the functional units of reinforcement. Our tests are based on the assumption that behavioral atoms may plausibly be represented at the neural level by individual cellular responses. As a first approach, we attempted to reinforce the bursting responses of hippocampal units in a highly reduced brain-slice preparation with local micropressure applications of behaviorally reinforcing dopaminergic drugs. The same injections were administered independently of bursting to provide a "noncontingent" control for nonspecific stimulation or facilitation of firing. It was found that the bursting responses of individual CA1 pyramidal neurons may be progressively facilitated in a dose-related manner by response-contingent (but not noncontingent) injections of dopamine itself, the dopamine D1-preferring agonist SKF 82958, the D3-preferring agonist quinpirole, and the D2-like selective agonist (+)-4-propyl-9 hydroxynapthoxazine. These findings support the conclusion that unit bursting responses can be reinforced in vitro in hippocampal slices, and they further suggest that the same dopamine receptor subtypes are involved in both cellular and behavioral operant conditioning. The results thus provide indirect support for Skinner's atoms-of-behavior hypothesis.

摘要

一种新颖的“体外强化”范式被用于研究斯金纳(1953)的假设:(a)操作性行为由极小的“反应元素”或“行为原子”组成;(b)这些非常小的单元而非整个反应是强化的功能单元。我们的测试基于这样一种假设,即行为原子在神经层面可能合理地由单个细胞反应来表示。作为第一种方法,我们试图在高度简化的脑片制备中,通过行为强化性多巴胺能药物的局部微压应用来强化海马体单元的爆发反应。相同的注射独立于爆发进行,以提供对非特异性刺激或放电促进的“非偶然”对照。结果发现,通过多巴胺本身、偏爱D1的多巴胺激动剂SKF 82958、偏爱D3的激动剂喹吡罗以及类D2选择性激动剂(+)-4-丙基-9-羟基萘并恶嗪的反应性(而非非偶然性)注射,单个CA1锥体神经元的爆发反应可能会以剂量相关的方式逐渐得到促进。这些发现支持了在体外海马体切片中单元爆发反应可被强化的结论,并且进一步表明相同的多巴胺受体亚型参与了细胞和行为操作性条件反射。因此,这些结果为斯金纳的行为原子假设提供了间接支持。

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