Evidence map›Paper›PMID 21483433›Full record

ArticleMolecular psychiatry2011

Selective deletion of the leptin receptor in dopamine neurons produces anxiogenic-like behavior and increases dopaminergic activity in amygdala.

J Liu, S M Perez, W Zhang, D J Lodge, X-Y Lu

Abstract read
In one paragraph

Article in Molecular psychiatry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

65 citing papers in PubMed, 118 citations in OpenAlex.

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  16. Obesity - A Matter of Motivation?Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association · 2022
    Review
  17. Review
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  19. Article
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5 more citing papers are in PubMed but not listed here.

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.

J LiuDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
S M Perez
W Zhang
D J Lodge
X-Y Lu
The University of Texas Health Science Center at San Antonio · US

Funding

Characterization of leptin's antidepressant activityR01MH076929 · NIMH · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LU, XIN-YUN · 2007 to 2016
$3.3M
Melanocortin system stress and HPA axisR01MH073844 · NIMH · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LU, XIN-YUN · 2006 to 2010
$1.3M
Attractin, Mahogunin, and NeurodegenerationR03NS056237 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ZHANG, WEI · 2007 to 2008
$146k
NIMH NIH HHS MH 073844NIMH NIH HHS MH 076929NIMH NIH HHS R01 MH073844NIMH NIH HHS R01 MH076929NINDS NIH HHS NS056237NINDS NIH HHS R03 NS056237
6 · The paper itself

Abstract

The leptin receptor (Lepr) is expressed on midbrain dopamine neurons. However, the specific role of Lepr signaling in dopamine neurons remains to be clarified. In the present study, we generated a line of conditional knockout mice lacking functional Lepr selectively on dopamine neurons (Lepr(DAT-Cre)). These mice exhibit normal body weight and feeding. Behaviorally, Lepr(DAT-Cre) mice display an anxiogenic-like phenotype in the elevated plus-maze, light-dark box, social interaction and novelty-suppressed feeding tests. Depression-related behaviors, as assessed by chronic stress-induced anhedonia, forced swim and tail-suspension tests, were not affected by deletion of Lepr in dopamine neurons. In vivo electrophysiological recordings of dopamine neurons in the ventral tegmental area revealed an increase in burst firing in Lepr(DAT-Cre) mice. Moreover, blockade of D1-dependent dopamine transmission in the central amygdala by local microinjection of the D1 antagonist SCH23390 attenuated the anxiogenic phenotype of Lepr(DAT-Cre) mice. These findings suggest that Lepr signaling in midbrain dopamine neurons has a crucial role for the expression of anxiety and for the dopamine modulation of amygdala function.

Indexed as

Action PotentialsAmygdalaAnimalsAnxietyDopamineDopaminergic NeuronsExploratory BehaviorInterpersonal RelationsMaze LearningMiceMice, KnockoutReceptors, LeptinSignal TransductionVentral Tegmental AreaDopamineReceptors, Leptin

Identifiers

PMID21483433
PMCPMC3432580
OpenAlexW2060925442

What OpenQuestion holds

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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.