1988
DOI: 10.1016/0006-8993(88)90768-8
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Stressful environmental stimuli increase extracellular DOPAC levels in the prefrontal cortex of hypoemotional (Roman high-avoidance) but not hyperemotional (Roman low-avoidance) rats. An in vivo voltammetric study

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Cited by 133 publications
(41 citation statements)
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“…A possible interpretation of this is that the septohippocampal system is involved in finding the appropriate coping reaction in an aversive situation (see also the theory by Gray [19]). According to D'Angio et al [9] also the medial prefrontal cortex plays a role in finding the appropriate coping strategy by way of influencing "attentional and/or cognitive processes in an attempt to deal with the stressor". The results of the present study, however, indicate that this is not true for the prelimbic area (it may well be true for the anterior cingulate area), because coping behavior was not influenced by the lesion.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…A possible interpretation of this is that the septohippocampal system is involved in finding the appropriate coping reaction in an aversive situation (see also the theory by Gray [19]). According to D'Angio et al [9] also the medial prefrontal cortex plays a role in finding the appropriate coping strategy by way of influencing "attentional and/or cognitive processes in an attempt to deal with the stressor". The results of the present study, however, indicate that this is not true for the prelimbic area (it may well be true for the anterior cingulate area), because coping behavior was not influenced by the lesion.…”
Section: Discussionmentioning
confidence: 99%
“…According to another view [31] it may have the function '*to update appropriate response outputs dependent on ..[the] internal state", which may among others be determined by the amygdala, which determines the 'emotional significance' of stimuli. Related to this is the opinion that the medial prefrontal cortex plays a role in stress responses [4], namely in finding appropriate coping reactions [9]. Besides these hypotheses, there are also those assigning to the prelimbic area a function in selecting responses in a working memory task context [18] or selecting 'cognitive strategies' [5].…”
Section: Introductionmentioning
confidence: 99%
“…Thus, it has been hypothesized that long-term exposure to drugs of abuse may alter the functional activity of dopaminergic afferent projections and glutamatergic neurons in frontocortical areas, with a consequent deficiency in the ability to inhibit inappropriate responses to drugs or drug-paired stimuli (Jentsch and Taylor, 1999;Everitt and Wolf, 2002;Chambers et al, 2003;Vanderschuren and Everitt, 2005). It is therefore noteworthy in this context that, compared with RLA rats, the mesocortical dopaminergic system of RHA rats is more robustly activated by both stressful and rewarding stimuli (D'Angio et al, 1988;Corda et al, 1997;Giorgi et al, 1999Giorgi et al, , 2003. In addition, RHA rats display higher scores than RLA rats in experimental paradigms used to assess sensation/ novelty seeking behavior in rodents (Siegel et al, 1993;Escorihuela et al, 1999;Fernández-Teruel et al, 2002;Steimer and Driscoll 2005).…”
Section: Figurementioning
confidence: 99%
“…Thus, compared with their RLA counterparts, RHA rats display a more robust sensation/novelty seeking profile, as well as higher baseline levels of impulsivity, and a marked preference for and intake of natural and drug rewards (Zeier et al, 1978;Siegel et al 1993;Escorihuela et al 1999;Giorgi et al 1999;Fernández-Teruel et al 2002). The phenotypic traits that distinguish these lines are at least partly determined by differences in the functional properties of their central dopaminergic pathways: (1) stressors and anxiogenic drugs activate the mesocortical dopaminergic projection of RHA, but not RLA, rats (D'Angio et al, 1988;Corda et al, 1997;Giorgi et al, 2003); (2) RHA rats have a higher density of D-1 dopamine (DA) receptors in the NAc (Giorgi et al, 1994); (3) the acute administration of psychostimulants and morphine causes a larger increment in motor activity and in DA output in the shell than in the core of the NAc of RHA, but not RLA, rats (Lecca et al, 2004); (4) the repeated administration of psychostimulants and morphine induces behavioral sensitization only in RHA rats Corda et al, 2005;Giorgi et al, 2005a); (5) in sensitized RHA rats, a subsequent challenge with these drugs elicits a more robust increment in DA output in the NAc-core, associated with an attenuated dopaminergic response in the NAc-shell, whereas these adaptive changes are not observed in sensitization-resistant RLA rats (Giorgi et al, 2005b(Giorgi et al, , 2007.…”
Section: Introductionmentioning
confidence: 99%
“…These findings suggest that RLA rats represent a valid genetic model to investigate the neural circuitry and molecular mechanisms underlying stress‐induced depression and, more specifically, to study depression associated with anxiety symptoms. Multidisciplinary studies aimed at identifying the central neuronal circuits involved in the above‐mentioned behavioral differences across the Roman lines have shown that their divergent phenotypic traits may be accounted for, at least in part, by differences in the functional responses of their central monoaminergic systems (D'Angiò, Serrano, Driscoll, & Scatton, 1988; Giorgi, Lecca, Piras, Driscoll, & Corda, 2003; Giorgi, Piras, Lecca, & Corda, 2005; Giorgi et al., 1994; Giorgi, Piras, et al., 2003 Giorgi et al., 2007, 2015; Lecca, Piras, Driscoll, Giorgi, & Corda, 2004; Sanna et al., 2015; Tournier et al., 2013). …”
Section: Introductionmentioning
confidence: 99%