IN VITRO REINFORCEMENT OF HIPPOCAMPAL BURSTING: A SEARCH FOR SKINNER'S ATOMS OF BEHAVIOR
- 1 March 1994
- journal article
- research article
- Published by Wiley in Journal of the Experimental Analysis of Behavior
- Vol. 61 (2) , 155-168
- https://doi.org/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.Keywords
This publication has 23 references indexed in Scilit:
- The D1 agonists SKF 82958 and SKF 77434 are self-administered by ratsBrain Research, 1992
- The Central Role of Voltage-Activated and Receptor-Operated Calcium Channels in Neuronal CellsAnnual Review of Pharmacology and Toxicology, 1992
- Receptor Subtypes in Opioid and Stimulant RewardBasic & Clinical Pharmacology & Toxicology, 1992
- Mechanisms Underlying Long-Term Potentiation of Synaptic TransmissionAnnual Review of Neuroscience, 1991
- Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neurolepticsNature, 1990
- Dopamine receptor agonists: selectivity and dopamine D1 receptor efficacyEuropean Journal of Pharmacology: Molecular Pharmacology, 1990
- Cellular investigations of behavioral reinforcementNeuroscience & Biobehavioral Reviews, 1989
- Distribution of opiate receptor subtypes and enkephalin and dynorphin immunoreactivity in the hippocampus of squirrel, guinea pig, rat, and hamsterJournal of Comparative Neurology, 1987
- Dopaminergic activity of substituted 6-chloro-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepinesJournal of Medicinal Chemistry, 1982
- Reward Schedules and Behavior Maintained by Intracranial Self-StimulationScience, 1955