Evidence map›Paper›PMID 27956741›Full record

ArticleMolecular psychiatry2017

Role of the adipose PPARγ-adiponectin axis in susceptibility to stress and depression/anxiety-related behaviors.

M Guo, C Li, Y Lei, S Xu, D Zhao, X-Y Lu

Open access · hybridAbstract read
In one paragraph

Article in Molecular psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 4% 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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 125 citations in OpenAlex.

  1. Pooled it
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20 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

6 authors at 3 institutions in 2 countries.

M GuoInstitute for Metabolic and Neuropsychiatric Disorders, Binzhou Medical University Hospital, Binzhou, China.
C LiInstitute for Metabolic and Neuropsychiatric Disorders, Binzhou Medical University Hospital, Binzhou, China.
Y LeiDepartment of Pharmacology, The University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
S XuInstitute for Metabolic and Neuropsychiatric Disorders, Binzhou Medical University Hospital, Binzhou, China.
D ZhaoInstitute for Metabolic and Neuropsychiatric Disorders, Binzhou Medical University Hospital, Binzhou, China.
X-Y LuInstitute for Metabolic and Neuropsychiatric Disorders, Binzhou Medical University Hospital, Binzhou, China.
Binzhou Medical University · CNBinzhou University · CNThe 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
Adiponectin signaling in mood regulationR01MH100583 · NIMH · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LU, XIN-YUN · 2013 to 2017
$1.9M
Adiponectin regulation of the mesolimbic dopamine systemR21MH096251 · NIMH · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LODGE, DANIEL, LU, XIN-YUN · 2012 to 2013
$399k
NIMH NIH HHS R01 MH076929NIMH NIH HHS R01 MH100583NIMH NIH HHS R21 MH096251
6 · The paper itself

Abstract

Adaptive responses to stressful stimuli involving behavioral, emotional and metabolic changes are orchestrated by the nervous and endocrine systems. Adipose tissue has been recognized as a highly active metabolic and endocrine organ, secreting adipokines that operate as hormones to mediate the crosstalk with other organs including the brain. The role of adipose tissue in sensing and responding to emotional stress and in behavioral regulation, however, remains largely unknown. The nuclear receptor peroxisome proliferator-activated receptor gamma (PPARγ) is a key transcriptional factor controlling adipokine gene expression. Here we show that chronic social defeat stress decreases messenger RNA and protein levels of PPARγ in adipose tissue of susceptible but not resilient mice, which was correlated with social avoidance behavior. A corresponding reduction in adipose adiponectin production was observed in susceptible mice. Rosiglitazone, a blood-brain barrier-impermeant PPARγ-selective agonist, elicited antidepressant- and anxiolytic-like behavioral effects in wild-type mice, with a concurrent increase in plasma adiponectin levels. These effects of rosiglitazone were absent in mice lacking adiponectin but having normal PPARγ expression in adipose tissue and brain. Moreover, pretreatment with the PPARγ-selective antagonist GW9662 blocked rosiglitazone-induced adiponectin expression and antidepressant/anxiolytic-like effects. Together, these results suggest that the behavioral responses to rosiglitazone are mediated through PPARγ-dependent induction of adiponectin. Our findings support an important role for the adipose PPARγ-adiponectin axis in susceptibility to stress and negative emotion-related behaviors. Selectively targeting PPARγ in adipose tissue may offer novel strategies for combating depression and anxiety.

Indexed as

AdipocytesAdiponectinAdipose TissueAdiposityAnimalsAnxietyBlood-Brain BarrierDepressionFemaleHypoglycemic AgentsMaleMiceMice, Inbred C57BLObesityPPAR gammaRNA, MessengerAdiponectinHypoglycemic AgentsPPAR gammaRNA, MessengerRosiglitazoneThiazolidinediones

Identifiers

PMID27956741
PMCPMC5468488
OpenAlexW2563054448

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.