Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2018 Mar:149:39-45.
doi: 10.1016/j.nlm.2018.02.001. Epub 2018 Feb 3.

Paradoxical accentuation of motivation following accumbens-pallidum disconnection

Affiliations

Paradoxical accentuation of motivation following accumbens-pallidum disconnection

Stephen E Chang et al. Neurobiol Learn Mem. 2018 Mar.

Abstract

The nucleus accumbens (NAc) and ventral pallidum (VP) are reciprocally connected, and activity within this circuit is thought to promote reward learning. Inconsistent with this notion, we find that disconnecting NAc medial shell and VP greatly enhances the attribution of value to a cue that is paired with reward. This result suggests that medial NAc shell and VP are both needed for attributing value to cues yet can also oppose one-another's functional contribution.

Keywords: Nucleus accumbens; Sign-tracking; Ventral pallidum.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest: The authors declare no competing financial interests.

Figures

Figure 1
Figure 1
Figure 1(a–b) AAV8-hSyn-hM4Di-mCitrine cell expression in all rats of Group Contra (a; n = 14) and Group Ipsi (b; n =12). Darker areas indicate common areas of overlap in terms of expression between rats. (c) Disconnection of NAc shell and VP dramatically enhanced the acquisition of sign-tracking. (d) Group Contra rats reached peak levels of sign-tracking 40% (4 days) faster compared to Group Ipsi rats. (e) Group Contra rats spent less time in the food cup overall compared to Group Ipsi rats. (f–g) Representative brain slice showing the area of AAV8-hSyn-hM4Di-mCitrine cell expression in the NAc shell (f) and VP (g).
Figure 2
Figure 2
Figure 2(a) AAV8-hSyn-hM4Di-mCitrine cell expression in all Group NAc-Gi rats (n = 7). Darker areas indicate common areas of overlap in terms of expression between rats. (b) Bilateral NAc shell inhibition had no effect on sign-tracking. (c) Bilateral NAc shell inhibition lowered food cup behavior non-discriminately.
Figure 3
Figure 3
Figure 3(a) Map of tetrode placements contralateral to hM4D(Gi) infusions, and recording timeline. (b–c) Populations of units that were excited, inhibited, or unaffected by CNO from recordings in the VP (t6=2.5, p = 0.047 population size comparison) and NAc (t6=0, p = 1). Number of units is shown below percentages (n = 3 rats; n = 26 NAc units, n = 20 VP units). (d–g) Real-time histograms (1-min bins; time zero = CNO) showing single units that were excited or inhibited in the VP and NAc. (h–k) Normalized firing rates (baseline-subtracted z-score) of pooled units with inhibition or excitation in NAc and VP.

Similar articles

Cited by

References

    1. Ahrens AM, Meyer PJ, Ferguson LM, Robinson TE, Aldridge JW. Neural activity in the ventral pallidum encodes variation in the incentive value of a reward cue. Journal of Neuroscience. 2016;36:7957–7970. - PMC - PubMed
    1. Armbruster BN, Li X, Pausch MH, Herlitze S, Roth BL. Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand. Proceedings of the National Academy of Sciences. 2007;104:5163–5168. - PMC - PubMed
    1. Berridge KC. Motivation concepts in behavioral neuroscience. Physiology & Behavior. 2004;81:179–209. - PubMed
    1. Chang SE, Holland PC. Effects of nucleus accumbens core and shell lesions on autoshaped lever-pressing. Behavioural Brain Research. 2013;256:36–42. - PMC - PubMed
    1. Chang SE, Todd TP, Bucci DJ, Smith KS. Chemogenetic manipulation of ventral pallidal neurons impairs acquisition of sign-tracking in rats. European Journal of Neuroscience. 2015;42:3105–3116. - PMC - PubMed

Publication types