2016
DOI: 10.1111/ejn.13358
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Dopaminergic neurotransmission in ventral and dorsal striatum differentially modulates alcohol reinforcement

Abstract: Dopaminergic neurotransmission in the striatum has been widely implicated in the reinforcing properties of substances of abuse. However, the striatum is functionally heterogeneous, and previous work has mostly focused on psychostimulant drugs. Therefore, we investigated how dopamine within striatal subregions modulates alcohol-directed behaviour in rats. We assessed the effects of infusion of the dopamine receptor antagonist alpha-flupenthixol into the shell and core of the nucleus accumbens (NAcc) and the dor… Show more

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Cited by 11 publications
(9 citation statements)
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References 88 publications
(122 reference statements)
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“…Indeed, across the literature, lower SB doses seem to suppress behavior involving other putative high-motivation states, including nicotine intake [181] and alcohol drinking in genetically-preferring rats [164]. Additionally, the NAcb shell [150,182] and Ox1Rs [183] regulate several types of compulsion-like behaviors, and the former is also a region where lower dose receptor inhibition can impact highereffort responding (progressive ratio), while higher antagonist doses are required to reduce lower-effort responding [184,185]. Thus, our interest in the NAcb shell as a regulator of compulsion-like drinking in both sexes remains.…”
Section: Systemic Test Of Orexin Receptor Regulation Of Binge and Compulsion-like Alcohol Drinkingmentioning
confidence: 99%
“…Indeed, across the literature, lower SB doses seem to suppress behavior involving other putative high-motivation states, including nicotine intake [181] and alcohol drinking in genetically-preferring rats [164]. Additionally, the NAcb shell [150,182] and Ox1Rs [183] regulate several types of compulsion-like behaviors, and the former is also a region where lower dose receptor inhibition can impact highereffort responding (progressive ratio), while higher antagonist doses are required to reduce lower-effort responding [184,185]. Thus, our interest in the NAcb shell as a regulator of compulsion-like drinking in both sexes remains.…”
Section: Systemic Test Of Orexin Receptor Regulation Of Binge and Compulsion-like Alcohol Drinkingmentioning
confidence: 99%
“…Interestingly, whereas inactivation of the DMS prevented the expression of an ethanol devaluation effect following 2 weeks of training, this manipulation was ineffective after 8 weeks of training when inactivation of the DLS restored sensitivity to devaluation 56 . Altogether, it is tempting to speculate that the higher motivation to consume ethanol in sensitized mice (compared with resistant mice) may be associated with habit learning processes and the abnormal response of the DLS that has also a well‐known role in incentive motivation 57 . It could be interesting to test in a future work whether targeting the DLS with lesions, denervation, or pharmacological inactivation could have an impact on the increased motivation for ethanol intake in sensitized mice.…”
Section: Discussionmentioning
confidence: 99%
“…The reason is that this slice contains the enlarged ventricle and the shrunk gray matter caused by alcoholism. On the contrary, hippocampus [36] and striatum [37] are also related to alcoholism. Nevertheless, their altered volumes are relatively small and hence do not provide an excellent performance in this task.…”
Section: Validation Of the Selected Slicementioning
confidence: 96%