» Articles » PMID: 35217811

Activation of Mesocorticolimbic Dopamine Projections Initiates Cue-induced Reinstatement of Reward Seeking in Mice

Overview
Specialty Pharmacology
Date 2022 Feb 26
PMID 35217811
Authors
Affiliations
Soon will be listed here.
Abstract

Drug addiction is characterized by relapse when addicts are re-exposed to drug-associated environmental cues, but the neural mechanisms underlying cue-induced relapse are unclear. In the present study we investigated the role of a specific dopaminergic (DA) pathway from ventral tegmental area (VTA) to nucleus accumbens core (NAcore) in mouse cue-induced relapse. Optical intracranial self-stimulation (oICSS) was established in DAT-Cre transgenic mice. We showed that optogenetic excitation of DA neurons in the VTA or their projection terminals in NAcore, NAshell or infralimbic prefrontal cortex (PFC-IL) was rewarding. Furthermore, activation of the VTA-NAcore pathway alone was sufficient and necessary to induce reinstatement of oICSS. In cocaine self-administration model, cocaine-associated cues activated VTA DA neurons as assessed by intracellular GCaMP signals. Cue-induced reinstatement of cocaine-seeking was triggered by optogenetic stimulation of the VTA-NAcore pathway, and inhibited by chemogenetic inhibition of this pathway. Together, these results demonstrate that cue-induced reinstatement of reward seeking is in part mediated by activation of the VTA-NAcore DA pathway.

Citing Articles

The nucleus accumbens in reward and aversion processing: insights and implications.

Xu Y, Lin Y, Yu M, Zhou K Front Behav Neurosci. 2024; 18:1420028.

PMID: 39184934 PMC: 11341389. DOI: 10.3389/fnbeh.2024.1420028.


Optical Intracranial Self-Stimulation (oICSS): A New Behavioral Model for Studying Drug Reward and Aversion in Rodents.

Song R, Soler-Cedeno O, Xi Z Int J Mol Sci. 2024; 25(6).

PMID: 38542425 PMC: 10970671. DOI: 10.3390/ijms25063455.


Advancing the preclinical study of comorbid neuroHIV and substance use disorders: Current perspectives and future directions.

Namba M, Xie Q, Barker J Brain Behav Immun. 2023; 113:453-475.

PMID: 37567486 PMC: 10528352. DOI: 10.1016/j.bbi.2023.07.021.


A neuropeptide signal confers ethanol state dependency during olfactory learning in .

Lindsay J, Mathies L, Davies A, Bettinger J Proc Natl Acad Sci U S A. 2022; 119(46):e2210462119.

PMID: 36343256 PMC: 9674237. DOI: 10.1073/pnas.2210462119.


Arecoline Induces an Excitatory Response in Ventral Tegmental Area Dopaminergic Neurons in Anesthetized Rats.

Lan Q, Guan P, Huang C, Huang S, Zhou P, Zhang C Front Pharmacol. 2022; 13:872212.

PMID: 35548350 PMC: 9081529. DOI: 10.3389/fphar.2022.872212.

References
1.
Kenny P, Hoyer D, Koob G . Animal Models of Addiction and Neuropsychiatric Disorders and Their Role in Drug Discovery: Honoring the Legacy of Athina Markou. Biol Psychiatry. 2018; 83(11):940-946. DOI: 10.1016/j.biopsych.2018.02.009. View

2.
Sinha R, Jastreboff A . Stress as a common risk factor for obesity and addiction. Biol Psychiatry. 2013; 73(9):827-35. PMC: 3658316. DOI: 10.1016/j.biopsych.2013.01.032. View

3.
Wolf M . Synaptic mechanisms underlying persistent cocaine craving. Nat Rev Neurosci. 2016; 17(6):351-65. PMC: 5466704. DOI: 10.1038/nrn.2016.39. View

4.
See R . Neural substrates of conditioned-cued relapse to drug-seeking behavior. Pharmacol Biochem Behav. 2002; 71(3):517-29. DOI: 10.1016/s0091-3057(01)00682-7. View

5.
Wilson S, Sayette M, Fiez J . Prefrontal responses to drug cues: a neurocognitive analysis. Nat Neurosci. 2004; 7(3):211-4. PMC: 2637355. DOI: 10.1038/nn1200. View