Elsevier

Brain Research

Volume 567, Issue 1, 13 December 1991, Pages 169-174
Brain Research

Dopaminergic activity is reduced in the prefrontal cortex and increased in the nucleus accumbens of rats predisposed to develop amphetamine self-administration

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Abstract

Individual vulnerability to the reinforcing effects of drugs appear to be a crucial factor in the development of addiction in humans. In the rat, individuals at risk for psychostimulant self-administration (SA) may be identified from their locomotor reactivity to a stress situation such as exposure to a novel environment. Animals with higher locomotor responses to novelty (High Responders, HR) tend to acquire amphetamine SA, while animals with the lower responses (Low Responders, LR) do not. In this study, we examined whether activity of dopaminergic (DA) and serotoninergic (5-HT) systems differed between HR and LR animals. These transmitter systems are thought to be involved in the reinforcing effects of psychostimulants. Animals from both groups were sacrificed under basal conditions and after exposure for 30 or 120 min to a novel environment, and the DA, 3,4-dihydroxyphenylacetic acid (DOPAC), 5-HT, and 5-hydroxyindolacetic acid (5-HIAA) contents were determined in the prefrontal cortex, nucleus accumbens and striatum. The HR rats displayed a specific neurochemical pattern: a higher DOPAC/DA ratio in the nucleus accumbens and striatum and a lower one in the prefrontal cortex. Furthermore, HR animals had lower overall 5-HT and 5-HIAA levels, corresponding to the mean of these compounds for the three structures studied over the three environmental conditions. Since similar DOPAC/DA ratios are found in animals in which the propensity to psychostimulants SA was induced by brain lesions of life events, an opposite pattern of dopaminergic activity in the prefrontal cortex (decrease) and in the ventral and dorsal striatum (increase) may be one of the neurobiological substrate of the predisposition to acquire amphetamine self-administration. The development of this difference may be influenced by interactions between dopaminergic and serotominergic systems. These results suggest that potential therapeutic strategies for the treatment of addiction will need to take into account the functional heterogeneity of projection systems rather than concentrate on a single neurotransmitter.

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    This work was supported by l'Institut National de la Santéet de la Recherche Médicale (INSERM) and l'Universitéde Bordeaux II.

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    We thank Isabelle Batby for secretarial assistance.

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