Evidence map›Paper›PMID 21726490›Full record

ArticleThe international journal of neuropsychopharmacology2012

Serotonin at the level of the amygdala and orbitofrontal cortex modulates distinct aspects of positive emotion in primates.

Mei-See Man, Yevheniia Mikheenko, Katrin Braesicke, Gemma Cockcroft, Angela C Roberts

Open access · hybridAbstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Anxiety and depression: A top-down, bottom-up model of circuit function.Annals of the New York Academy of Sciences · 2023
    Review
  2. Review
  3. Input-specific contributions to valence processing in the amygdala.Learning & memory (Cold Spring Harbor, N.Y.) · 2016
    Review
  4. Article
  5. Review
  6. Serotonin and aversive Pavlovian control of instrumental behavior in humans.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  7. Review
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Mei-See ManDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge, UK.
Yevheniia MikheenkoDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge, UK.
Katrin BraesickeDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge, UK.
Gemma CockcroftBehavioural and Clinical Neurosciences Institute, University of Cambridge, Downing Street, UK.
Angela C RobertsDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge, UK.
University of Cambridge · GB

Funding

Medical Research Council G0001354Medical Research Council G0401411Medical Research Council G0901884Medical Research Council G1000183Wellcome Trust 093875
6 · The paper itself

Abstract

Impaired top-down regulation of the amygdala, and its modulation by serotonin (5-HT), is strongly implicated in the dysregulation of negative emotion that characterizes a number of affective disorders. However, the contribution of these mechanisms to the regulation of positive emotion is not well understood. This study investigated the role of 5-HT within the amygdala and the orbitofrontal cortex (OFC), on the expression of appetitive Pavlovian conditioned emotional responses and their reversal in a primate, the common marmoset. Its effects were compared to those of the amygdala itself. Having developed conditioned autonomic and behavioural responses to an appetitive cue prior to surgery, marmosets with excitotoxic amygdala lesions failed to display such conditioned autonomic arousal at retention, but still displayed intact cue-directed conditioned behaviours. In contrast, 5,7-DHT infusions into the amygdala, reducing extracellular 5-HT levels, selectively enhanced the expression of appetitive conditioned behaviour at retention. Similar infusions into the OFC, producing marked reductions in post-mortem 5-HT tissue levels, had no overall effect on autonomic or behavioural responses, either at retention or during reversal learning, but caused an uncoupling of these responses, thereby fractionating emotional output. These data demonstrate the critical role of the amygdala in the expression of appetitive autonomic conditioning, and the region-selective contribution of 5-HT in the amygdala and OFC, respectively, to the expression of conditioned behaviour and the overall coordination of the emotional response. They provide insight into the neurochemical mechanisms underlying the regulation of positive emotional responses, advancing our understanding of the neural basis of pathologically dysregulated emotion.

Indexed as

5,7-DihydroxytryptamineAmygdalaAnimalsAppetitive BehaviorCallithrixCardiovascular Physiological PhenomenaConditioning, ClassicalCuesEmotionsExtracellular SpaceFemaleFrontal LobeHydroxyindoleacetic AcidMaleMotor ActivityNeurotoxins5,7-DihydroxytryptamineHydroxyindoleacetic AcidNeurotoxinsSerotoninSerotonin Agents

Identifiers

PMID21726490
PMCPMC3243904
OpenAlexW2100342300

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.